Search by Gene
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1581 | 272 | 79 | 51 | 99 | 13 | 28 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0002 | 0/0 | 1581 | 3 | 3 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0003 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0004 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0005 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0006 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0007 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4746 | 256 | 66 | 51 | 99 | 12 | 26 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0002 | 0/0 | 4746 | 13 | 11 | 0 | 0 | 1 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0003 | 0/0 | 4746 | 3 | 3 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0004 | 0/0 | 4746 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0005 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0006 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0007 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0008 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0009 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| c0010 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3392 | 136 | 26 | 31 | 52 | 7 | 18 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0002 | 0/0 | 3392 | 112 | 46 | 17 | 40 | 5 | 4 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0003 | 0/0 | 3392 | 5 | 0 | 1 | 0 | 1 | 3 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0004 | 0/0 | 3391 | 5 | 5 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0005 | 0/0 | 3392 | 4 | 0 | 0 | 4 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0006 | 0/0 | 3393 | 3 | 3 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0007 | 0/0 | 3393 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0008 | 0/0 | 3392 | 2 | 0 | 0 | 0 | 1 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0009 | 0/0 | 3392 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0010 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0011 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0012 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0013 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0014 | 0/0 | 3392 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0015 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0016 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0017 | 0/0 | 3392 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0018 | 0/0 | 3391 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| t0019 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 256 | 66 | 51 | 99 | 12 | 26 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 13 | 11 | 0 | 0 | 1 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0003c0005 | a0003 | c0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0004c0007 | a0004 | c0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0005c0009 | a0005 | c0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0006c0006 | a0006 | c0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0007c0010 | a0007 | c0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 133 | 24 | 31 | 51 | 7 | 18 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 98 | 35 | 17 | 38 | 4 | 4 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0002t0006 | a0001 | c0002 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0002t0008 | a0001 | c0002 | t0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0001c0008t0017 | a0001 | c0008 | t0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0002c0003t0002 | a0002 | c0003 | t0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0002c0003t0015 | a0002 | c0003 | t0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0003c0005t0002 | a0003 | c0005 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0004c0007t0010 | a0004 | c0007 | t0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0005c0009t0002 | a0005 | c0009 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0006c0006t0002 | a0006 | c0006 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| a0007c0010t0001 | a0007 | c0010 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0259 | a0001 | c0001 | t0001 | g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0001g0273 | a0001 | c0001 | t0001 | g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0152 | a0001 | c0001 | t0002 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0153 | a0001 | c0001 | t0002 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0154 | a0001 | c0001 | t0002 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0155 | a0001 | c0001 | t0002 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0156 | a0001 | c0001 | t0002 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0158 | a0001 | c0001 | t0002 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0159 | a0001 | c0001 | t0002 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0160 | a0001 | c0001 | t0002 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0161 | a0001 | c0001 | t0002 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0163 | a0001 | c0001 | t0002 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0164 | a0001 | c0001 | t0002 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0166 | a0001 | c0001 | t0002 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0167 | a0001 | c0001 | t0002 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0168 | a0001 | c0001 | t0002 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0169 | a0001 | c0001 | t0002 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0170 | a0001 | c0001 | t0002 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0171 | a0001 | c0001 | t0002 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0172 | a0001 | c0001 | t0002 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0173 | a0001 | c0001 | t0002 | g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0174 | a0001 | c0001 | t0002 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0175 | a0001 | c0001 | t0002 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0181 | a0001 | c0001 | t0002 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0182 | a0001 | c0001 | t0002 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0183 | a0001 | c0001 | t0002 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0184 | a0001 | c0001 | t0002 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0185 | a0001 | c0001 | t0002 | g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0186 | a0001 | c0001 | t0002 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0187 | a0001 | c0001 | t0002 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0188 | a0001 | c0001 | t0002 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0190 | a0001 | c0001 | t0002 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0191 | a0001 | c0001 | t0002 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0193 | a0001 | c0001 | t0002 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0194 | a0001 | c0001 | t0002 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0195 | a0001 | c0001 | t0002 | g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0200 | a0001 | c0001 | t0002 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0201 | a0001 | c0001 | t0002 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0202 | a0001 | c0001 | t0002 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0204 | a0001 | c0001 | t0002 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0207 | a0001 | c0001 | t0002 | g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0208 | a0001 | c0001 | t0002 | g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0209 | a0001 | c0001 | t0002 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0210 | a0001 | c0001 | t0002 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0211 | a0001 | c0001 | t0002 | g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0212 | a0001 | c0001 | t0002 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0213 | a0001 | c0001 | t0002 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0214 | a0001 | c0001 | t0002 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0215 | a0001 | c0001 | t0002 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0216 | a0001 | c0001 | t0002 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0217 | a0001 | c0001 | t0002 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0218 | a0001 | c0001 | t0002 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0220 | a0001 | c0001 | t0002 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0221 | a0001 | c0001 | t0002 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0222 | a0001 | c0001 | t0002 | g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0224 | a0001 | c0001 | t0002 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0225 | a0001 | c0001 | t0002 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0226 | a0001 | c0001 | t0002 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0227 | a0001 | c0001 | t0002 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0228 | a0001 | c0001 | t0002 | g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0229 | a0001 | c0001 | t0002 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0230 | a0001 | c0001 | t0002 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0231 | a0001 | c0001 | t0002 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0233 | a0001 | c0001 | t0002 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0235 | a0001 | c0001 | t0002 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0237 | a0001 | c0001 | t0002 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0238 | a0001 | c0001 | t0002 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0239 | a0001 | c0001 | t0002 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0241 | a0001 | c0001 | t0002 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0242 | a0001 | c0001 | t0002 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0243 | a0001 | c0001 | t0002 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0246 | a0001 | c0001 | t0002 | g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0247 | a0001 | c0001 | t0002 | g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0248 | a0001 | c0001 | t0002 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0250 | a0001 | c0001 | t0002 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0251 | a0001 | c0001 | t0002 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0252 | a0001 | c0001 | t0002 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0253 | a0001 | c0001 | t0002 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0254 | a0001 | c0001 | t0002 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0255 | a0001 | c0001 | t0002 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0256 | a0001 | c0001 | t0002 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0257 | a0001 | c0001 | t0002 | g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0266 | a0001 | c0001 | t0002 | g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0267 | a0001 | c0001 | t0002 | g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0268 | a0001 | c0001 | t0002 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0002g0269 | a0001 | c0001 | t0002 | g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0003g0012 | a0001 | c0001 | t0003 | g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0003g0013 | a0001 | c0001 | t0003 | g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0003g0014 | a0001 | c0001 | t0003 | g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0003g0016 | a0001 | c0001 | t0003 | g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0004g0157 | a0001 | c0001 | t0004 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0004g0162 | a0001 | c0001 | t0004 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0004g0165 | a0001 | c0001 | t0004 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0004g0240 | a0001 | c0001 | t0004 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0004g0244 | a0001 | c0001 | t0004 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0005g0043 | a0001 | c0001 | t0005 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0005g0091 | a0001 | c0001 | t0005 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0005g0119 | a0001 | c0001 | t0005 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0005g0124 | a0001 | c0001 | t0005 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0006g0236 | a0001 | c0001 | t0006 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0007g0009 | a0001 | c0001 | t0007 | g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0007g0136 | a0001 | c0001 | t0007 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0009g0090 | a0001 | c0001 | t0009 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0011g0051 | a0001 | c0001 | t0011 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0012g0123 | a0001 | c0001 | t0012 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0013g0234 | a0001 | c0001 | t0013 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0014g0118 | a0001 | c0001 | t0014 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0016g0249 | a0001 | c0001 | t0016 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0018g0060 | a0001 | c0001 | t0018 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0001t0019g0275 | a0001 | c0001 | t0019 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0005 | a0001 | c0002 | t0002 | g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0006 | a0001 | c0002 | t0002 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0180 | a0001 | c0002 | t0002 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0260 | a0001 | c0002 | t0002 | g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0261 | a0001 | c0002 | t0002 | g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0262 | a0001 | c0002 | t0002 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0263 | a0001 | c0002 | t0002 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0002g0265 | a0001 | c0002 | t0002 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0006g0178 | a0001 | c0002 | t0006 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0006g0274 | a0001 | c0002 | t0006 | g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0008g0179 | a0001 | c0002 | t0008 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0002t0008g0264 | a0001 | c0002 | t0008 | g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0004t0001g0149 | a0001 | c0004 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0004t0001g0150 | a0001 | c0004 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0001c0008t0017g0075 | a0001 | c0008 | t0017 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 |
| a0002c0003t0002g0232 | a0002 | c0003 | t0002 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0002c0003t0002g0271 | a0002 | c0003 | t0002 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0002c0003t0015g0270 | a0002 | c0003 | t0015 | g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0003c0005t0002g0196 | a0003 | c0005 | t0002 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0004c0007t0010g0007 | a0004 | c0007 | t0010 | g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0005c0009t0002g0245 | a0005 | c0009 | t0002 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0006c0006t0002g0205 | a0006 | c0006 | t0002 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| a0007c0010t0001g0015 | a0007 | c0010 | t0001 | g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | MED1_chr17_39399285_39456263 | MED1 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | MED1_chr17_39399285_39456263 | MED1 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | MED1_chr17_39399285_39456263 | MED1 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | FIN | MED1_chr17_39399285_39456263 | MED1 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01081 | hp2 | a0004 | c0007 | t0010 | g0007 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01192 | hp2 | a0001 | c0001 | t0014 | g0118 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0237 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 |
| HG01516 | hp1 | a0006 | c0006 | t0002 | g0205 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG02004 | hp2 | a0001 | c0001 | t0009 | g0090 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0150 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0149 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CDX | MED1_chr17_39399285_39456263 | MED1 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | MED1_chr17_39399285_39456263 | MED1 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02258 | hp2 | a0002 | c0003 | t0015 | g0270 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02523 | hp1 | a0001 | c0001 | t0019 | g0275 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02647 | hp1 | a0002 | c0003 | t0002 | g0232 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02738 | hp1 | a0001 | c0002 | t0008 | g0179 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0263 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0274 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0260 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG03195 | hp2 | a0002 | c0003 | t0002 | g0271 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0234 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03491 | hp2 | a0001 | c0001 | t0018 | g0060 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 |
| HG03654 | hp1 | a0001 | c0008 | t0017 | g0075 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18961 | hp2 | a0007 | c0010 | t0001 | g0015 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18966 | hp1 | a0003 | c0005 | t0002 | g0196 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18971 | hp2 | a0001 | c0001 | t0011 | g0051 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19006 | hp2 | a0005 | c0009 | t0002 | g0245 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19007 | hp2 | a0001 | c0001 | t0016 | g0249 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19009 | hp1 | a0001 | c0001 | t0012 | g0123 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0178 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | MED1_chr17_39399285_39456263 | MED1 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ASW | MED1_chr17_39399285_39456263 | MED1 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 |
| NA20752 | hp2 | a0001 | c0002 | t0008 | g0264 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | MED1_chr17_39399285_39456263 | MED1 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | GIH | MED1_chr17_39399285_39456263 | MED1 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0151 | REF | REF | MED1_chr17_39399285_39456263 | MED1 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0223 | REF | REF | MED1_chr17_39399285_39456263 | MED1 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:39407536
|
G | A | 1 | a0004 | 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 | a0005 | 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 | a0006 | 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 | a0007 | 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 | a0003 | 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 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | 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 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:39404520
|
T | C | 1 | a0004c0007t0010 | 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 | a0004c0007t0010 | 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 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(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 | a0001c0001t0019 | 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 | a0001c0001t0011a0001c0001t0012 | 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 | a0001c0001t0006a0001c0001t0007a0001c0002t0006others(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 | a0001c0001t0004a0001c0001t0018 | 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 | a0001c0001t0019 | 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 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:39410897
|
C | T | 1 | a0001c0001t0002g0181 | 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 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0086others(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 | a0001c0001t0001g0088 | 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 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0180others(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 | a0001c0001t0002g0167a0001c0001t0002g0184a0001c0001t0002g0185others(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 | a0001c0001t0002g0171 | 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 | a0001c0001t0001g0056a0001c0001t0001g0089a0001c0001t0001g0110others(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 | a0002c0003t0002g0232a0002c0003t0002g0271a0002c0003t0015g0270 | 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 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0001c0001t0002g0212 | 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1500-1286delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412006 | ||||||
| chr17:39412038
|
G | C | 1 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0089a0001c0001t0002g0152a0001c0001t0002g0153others(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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0001g0103a0001c0001t0001g0108 | 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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0001g0073a0001c0001t0001g0115a0001c0001t0001g0129others(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 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(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 | a0001c0001t0001g0041a0001c0001t0002g0241a0001c0001t0004g0244 | 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 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0002g0201others(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 | a0001c0001t0004g0157a0001c0001t0004g0165 | 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0002g0207 | 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 | a0001c0001t0004g0240 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0002g0247 | 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 | a0001c0001t0002g0169a0001c0001t0002g0173a0001c0001t0002g0208others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0001g0272a0001c0001t0002g0169a0001c0001t0002g0173others(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 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0025others(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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): 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 | a0001c0001t0002g0231 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0041a0001c0001t0001g0112a0001c0001t0002g0216others(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 | a0001c0001t0001g0017 | 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0002g0002a0001c0001t0002g0169a0001c0001t0002g0170others(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 | a0001c0001t0002g0174a0001c0001t0002g0201a0001c0001t0002g0204others(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 | a0001c0001t0002g0168 | 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 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0187others(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 | a0001c0001t0001g0176a0001c0001t0001g0259a0001c0001t0002g0230others(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 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0156others(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 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0135others(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 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(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 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(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 | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(53): 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 | a0001c0001t0007g0009 | 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 | a0001c0001t0002g0248 | 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 | a0001c0001t0002g0003a0001c0001t0002g0200a0001c0001t0002g0202others(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 | a0001c0001t0002g0004a0001c0001t0002g0195a0001c0001t0002g0214others(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 | a0001c0001t0002g0160 | 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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0161others(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 | a0001c0001t0002g0231 | 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 | a0001c0001t0002g0257a0001c0002t0006g0178a0001c0002t0008g0179 | 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 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0241others(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 | a0004c0007t0010g0007 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0001g0097a0001c0001t0001g0114a0001c0001t0001g0129 | 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 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0086others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0001g0116 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1298-333A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415672 | ||||||
| chr17:39415674
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0001g0258 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0044others(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 | a0001c0001t0004g0157a0001c0001t0004g0165 | 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 | a0001c0001t0001g0052a0001c0001t0001g0176a0001c0001t0001g0177others(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 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(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 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0156others(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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0002g0218a0001c0001t0002g0246a0001c0001t0002g0247others(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 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0001c0001t0001g0010 | 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 | 196 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(193): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1298-1473T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39416812 | ||||||
| chr17:39416893
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0135 | 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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1298-1853A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417192 | ||||||
| chr17:39417193
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1298-1854C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417193 | ||||||
| chr17:39417263
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0001g0070a0001c0001t0002g0152a0001c0001t0002g0153others(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 | a0001c0001t0002g0246 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0002g0246 | 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0002g0255 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0002g0152others(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 | a0001c0001t0001g0078a0001c0001t0001g0127a0001c0001t0002g0159others(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 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(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 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0025others(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 | 14 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0030others(11): Show | 14 | HG00741.hp2 HG01071.hp1 HG01243.hp1 others(11): 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0001g0019a0001c0001t0001g0134 | 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 | 144 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): 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 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(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 | a0001c0001t0004g0165 | 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0002g0167a0001c0001t0002g0188 | 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 | a0001c0001t0001g0258 | 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 | a0001c0002t0002g0265 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0018others(140): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1297+927dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418789 | ||||||
| chr17:39418789
|
A | ATT | 7 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0115others(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 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0132 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0154a0001c0001t0002g0182a0001c0001t0002g0183others(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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | 150 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): 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 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0002g0152others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0130 | 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0001g0077a0001c0001t0001g0122a0001c0001t0001g0126others(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 | a0001c0001t0001g0034a0001c0001t0001g0067a0001c0001t0001g0114others(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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0013g0234 | 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 | a0001c0008t0017g0075 | 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 | a0001c0001t0004g0165 | 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 | 162 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1096-874dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420791 | ||||||
| chr17:39420791
|
A | ATT | 6 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0125others(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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0002g0225a0001c0001t0002g0228 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0016g0249 | 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 | a0001c0001t0002g0170 | 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 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0042 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1096-1288C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421206 | ||||||
| chr17:39421231
|
C | A | 274 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(271): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1096-1313G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421231 | ||||||
| chr17:39421238
|
C | CA | 17 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0053others(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 | a0001c0001t0002g0230 | 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 | a0001c0001t0013g0234 | 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 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0255others(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 | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1095+1424G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421903 | ||||||
| chr17:39422127
|
CA | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1095+1199delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422127 | ||||||
| chr17:39422181
|
T | C | 1 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | 58 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(55): Show | 58 | HG00423.hp2 HG01081.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1095+857dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422469 | ||||||
| chr17:39422469
|
G | GTT | 5 | a0001c0001t0001g0082a0001c0001t0001g0115a0001c0001t0002g0152others(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 | a0001c0001t0002g0241a0001c0001t0004g0244 | 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 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0023others(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 | 67 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(64): Show | 68 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(65): 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 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0221others(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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0109a0001c0001t0001g0141 | 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 | a0001c0001t0001g0109a0001c0001t0001g0141 | 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 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0068others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0061 | 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 | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): 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 | a0001c0001t0002g0216 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0002g0154a0001c0001t0002g0164 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0002g0154a0001c0001t0002g0164a0001c0001t0002g0166 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0002g0266a0001c0001t0002g0267 | 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 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0002g0181 | 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 | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0135others(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 | a0001c0001t0001g0056a0001c0001t0001g0176a0001c0001t0001g0177others(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 | a0001c0001t0002g0246 | 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 | a0001c0001t0002g0167 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0002t0002g0263a0001c0002t0006g0178a0001c0002t0006g0274 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0004g0157a0001c0001t0004g0165 | 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0002g0167a0001c0001t0002g0184a0001c0001t0002g0185others(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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0057 | 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 | a0004c0007t0010g0007 | 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 | a0003c0005t0002g0196 | 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 | a0001c0001t0001g0010a0001c0001t0001g0070 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0002g0210a0001c0001t0002g0215a0001c0001t0002g0219 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0237 | 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 | a0001c0001t0001g0097a0001c0001t0001g0114a0001c0001t0001g0129 | 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 | a0001c0001t0002g0163 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0002t0008g0264 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084 | 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 | 194 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(191): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): 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 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0257 | 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 | a0001c0001t0002g0212 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | 140 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.649+1412dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429702 | ||||||
| chr17:39429702
|
T | TAA | 34 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(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 | a0001c0001t0002g0269 | 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0001g0128 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0182a0001c0001t0002g0183 | 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 | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0002g0171 | 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 | 188 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(185): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.649+422delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430692 | ||||||
| chr17:39430744
|
G | A | 3 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0002g0204 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.576-94delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 8/16 | chr17 | 39431281 | ||||||
| chr17:39431288
|
T | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0115 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0083others(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 | 182 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(179): Show | 184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0001t0001g0072 | 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 | 146 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0059a0001c0001t0001g0137a0001c0001t0002g0215others(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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0259others(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 | a0001c0001t0002g0181 | 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0089a0001c0001t0001g0110a0001c0001t0001g0120 | 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 | a0001c0001t0002g0154a0001c0001t0002g0164 | 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 | a0001c0001t0002g0239 | 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 | a0001c0001t0013g0234 | 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 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0002g0194others(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 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0055others(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 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0107others(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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0156others(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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084 | 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 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0273 | 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 | a0004c0007t0010g0007 | 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 | a0001c0002t0002g0263 | 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 | a0001c0001t0002g0255 | 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 | a0001c0001t0002g0255 | 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 | a0001c0001t0001g0045a0001c0001t0001g0067 | 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 | 146 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): 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 | a0001c0001t0002g0201 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0002g0191 | 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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): 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 | a0001c0001t0002g0163 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0107a0001c0001t0001g0108 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0001c0001t0001g0107a0001c0001t0001g0108 | 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 | a0001c0001t0001g0148a0001c0004t0001g0149a0001c0004t0001g0150 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0266a0001c0001t0002g0267 | 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 | a0001c0001t0002g0266a0001c0001t0002g0267 | 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 | 153 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(150): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.429-2050delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436369 | ||||||
| chr17:39436467
|
C | T | 1 | a0001c0001t0001g0112 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0258others(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 | a0001c0001t0002g0152 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0085a0001c0002t0008g0264 | 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 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0255others(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 | a0001c0001t0001g0045a0001c0001t0001g0067 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0258others(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 | a0001c0001t0002g0213 | 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 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0061others(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 | a0001c0001t0002g0171 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0002g0267 | 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 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(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 | a0001c0001t0001g0272 | 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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): 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 | a0001c0001t0001g0133a0001c0001t0002g0152a0001c0001t0002g0153others(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 | a0001c0001t0002g0167a0001c0001t0002g0190a0001c0001t0002g0193others(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 | 150 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(147): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.428+827delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438337 | ||||||
| chr17:39438337
|
ATT | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0258others(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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0002g0167a0001c0001t0002g0188 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0002g0198 | 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 | a0001c0001t0002g0154a0001c0001t0002g0164a0001c0001t0002g0166 | 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 | a0001c0001t0001g0046a0001c0001t0001g0148a0001c0001t0002g0181others(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 | a0001c0001t0002g0171a0001c0001t0002g0182a0001c0001t0002g0183others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(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 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0070others(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 | a0001c0001t0001g0258a0001c0001t0002g0185a0001c0001t0002g0186others(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 | a0001c0001t0002g0239a0001c0001t0002g0252a0001c0001t0002g0256 | 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 | a0001c0001t0001g0259a0001c0001t0002g0251a0001c0001t0002g0253others(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 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0002g0171others(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 | a0001c0001t0001g0048a0001c0001t0001g0107a0001c0001t0001g0108others(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 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0156others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0040a0001c0001t0001g0095a0001c0001t0001g0096others(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 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0002g0250 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(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 | a0001c0001t0002g0250 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053 | 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 | a0001c0001t0002g0171a0004c0007t0010g0007 | 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 | a0004c0007t0010g0007 | 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 | a0004c0007t0010g0007 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0004g0157a0001c0001t0004g0165a0004c0007t0010g0007 | 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 | a0004c0007t0010g0007 | 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 | a0001c0002t0002g0260 | 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 | 271 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(268): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0258others(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 | a0001c0001t0011g0051 | 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 | a0001c0001t0001g0107a0001c0001t0001g0108 | 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 | a0001c0001t0002g0194a0001c0001t0002g0250a0001c0001t0002g0251others(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 | 196 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(193): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): 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 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0086others(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 | a0001c0001t0001g0042a0001c0001t0001g0117a0001c0001t0001g0132 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0258others(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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.212-818G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441495 | ||||||
| chr17:39441586
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(193): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): 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 | a0001c0001t0001g0023 | 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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0047others(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 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(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 | a0001c0001t0001g0130 | 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 | 203 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(200): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): 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 | a0001c0001t0001g0259a0001c0001t0002g0152a0001c0001t0002g0155others(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 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0145others(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 | a0004c0007t0010g0007 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0026others(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 | a0001c0001t0001g0050a0001c0001t0001g0148a0001c0001t0002g0152others(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 | a0001c0001t0001g0272 | 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 | 92 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0036others(89): Show | 95 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.211+553dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442996 | ||||||
| chr17:39442996
|
C | CTT | 26 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0002g0257 | 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 | a0001c0001t0001g0036 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0109a0001c0001t0001g0141 | 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 | a0001c0001t0002g0182a0001c0001t0002g0183 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0102a0001c0001t0001g0103 | 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 |
196 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(193): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): 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 | a0001c0001t0001g0107a0001c0001t0001g0108 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0145 | 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 | a0005c0009t0002g0245 | 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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0166 | 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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.133-1236T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444864 | ||||||
| chr17:39444894
|
C | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(141): 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 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(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 | a0001c0001t0001g0106a0001c0001t0001g0176a0001c0001t0001g0177others(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 | a0001c0001t0001g0104a0001c0001t0001g0140 | 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 | a0001c0001t0002g0226 | 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 | 196 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(193): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): 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 | a0001c0001t0002g0181 | 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 | a0001c0001t0002g0241a0001c0001t0004g0244 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039 | 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 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0002g0152others(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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0258others(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 | a0001c0001t0001g0148a0001c0001t0001g0272a0001c0001t0002g0153others(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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 103 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.132+1348delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446449 | ||||||
| chr17:39446508
|
G | A | 1 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0229 | 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 | 204 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(201): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.132+656C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447142 | ||||||
| chr17:39447334
|
T | G | 1 | a0001c0001t0001g0151 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.132+464A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447334 | ||||||
| chr17:39447387
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.132+411C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447387 | ||||||
| chr17:39447394
|
T | TA | 162 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(159): Show | 163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.132+403dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447394 | ||||||
| chr17:39447521
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0258others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0002g0181others(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 | a0004c0007t0010g0007 | 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 | a0001c0001t0002g0152a0001c0001t0002g0159a0001c0001t0002g0160others(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 | a0001c0001t0002g0167a0001c0001t0002g0184a0001c0001t0002g0185others(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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(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 | a0001c0001t0001g0177a0001c0001t0001g0258a0001c0001t0001g0259others(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 | a0001c0001t0002g0182a0001c0001t0002g0183 | 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 | a0001c0001t0002g0266a0001c0001t0002g0267 | 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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0004c0007t0010g0007 | 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 | a0001c0001t0001g0024 | 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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0002g0181 | 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 | 146 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.25+1523delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449514 | ||||||
| chr17:39449809
|
C | CT | 18 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0272others(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 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(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 | ||||||
| chr17:39449809
|
CTT | C | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0151others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+1227_25+1228del others(2): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449809 | ||||||
| chr17:39449839
|
A | G | 15 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0154others(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 | a0004c0007t0010g0007 | 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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): 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 | 146 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.25+915dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39450122 | ||||||
| chr17:39450180
|
G | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): 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 | a0001c0001t0001g0272a0001c0001t0001g0273 | 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 | a0001c0002t0006g0274 | 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 | a0004c0007t0010g0007 | 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 |