Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9441 |
|---|---|
| ensemblid | ENSG00000105085.11 |
| hgncid | 2376 |
| symbol | MED26 |
| name | mediator complex subunit 26 |
| refseq_nuc | NM_004831.5 |
| refseq_prot | NP_004822.2 |
| ensembl_nuc | ENST00000263390.8 |
| ensembl_prot | ENSP00000263390.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 16574919 |
| end | 16628204 |
| strand | - |
| ver | v1.2 |
| region | chr19:16574919-16628204 |
| region5000 | chr19:16569919-16633204 |
| regionname0 | MED26_chr19_16574919_16628204 |
| regionname5000 | MED26_chr19_16569919_16633204 |
| ahapid | grch38/chm13v2 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 | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 600 | 265 | 77 | 62 | 78 | 6 | 40 | 46 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0002 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0003 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0004 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1803 | 248 | 64 | 60 | 77 | 6 | 39 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0002 | 0/0 | 1803 | 12 | 11 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0003 | 0/0 | 1803 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0004 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0005 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0006 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0007 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0008 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| c0009 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| thapid | grch38chm13v2 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1370 | 249 | 68 | 58 | 77 | 6 | 38 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0002 | 0/0 | 1369 | 12 | 8 | 3 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0003 | 0/0 | 1369 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0004 | 0/0 | 1370 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0005 | 0/0 | 1369 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0006 | 0/0 | 1370 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0007 | 0/0 | 1370 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0008 | 0/0 | 1370 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| t0009 | 0/0 | 1370 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0002 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0004 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0005 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0006 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| achapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1803 | 248 | 64 | 60 | 77 | 6 | 39 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0002 | 0/0 | 1803 | 12 | 11 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0003 | 0/0 | 1803 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0005 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0006 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0009 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0002c0004 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0003c0007 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0004c0008 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3172 | 231 | 54 | 56 | 76 | 6 | 37 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0001t0002 | 0/0 | 3171 | 11 | 7 | 3 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0001t0004 | 0/0 | 3172 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0001t0005 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0001t0006 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0001t0007 | 0/0 | 3172 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0001t0008 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0001t0009 | 0/0 | 3172 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0002t0001 | 0/0 | 3172 | 12 | 11 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0003t0001 | 0/0 | 3172 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0005t0003 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0006t0001 | 0/0 | 3172 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0001c0009t0001 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0002c0004t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0003c0007t0001 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| a0004c0008t0001 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | copy fasta | chr19 | 16569919 | 16633204 |
| actghapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0005 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0003t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0005t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0009t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0002c0004t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0003c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0004c0008t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0148 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02280 | hp1 | a0001 | c0005 | t0003 | g0077 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0186 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02922 | hp2 | a0003 | c0007 | t0001 | g0029 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02965 | hp1 | a0001 | c0009 | t0001 | g0142 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02976 | hp1 | a0004 | c0008 | t0001 | g0092 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03516 | hp2 | a0002 | c0004 | t0002 | g0214 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0023 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18949 | hp1 | a0001 | c0006 | t0001 | g0082 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | USA | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0199 | REF | REF | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0175 | REF | REF | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16576265
|
C | T | 1 | a0003 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1565G>A | p.Arg522Gln | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1826/3172 | 1565/1803 | 522/600 | chr19 | 16576265 | ||
| chr19:16576775
|
G | A | 1 | a0004 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1055C>T | p.Ala352Val | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1316/3172 | 1055/1803 | 352/600 | chr19 | 16576775 | ||
| chr19:16578405
|
C | T | 1 | a0002 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.77G>A | p.Arg26Gln | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/3 | 338/3172 | 77/1803 | 26/600 | chr19 | 16578405 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16576591
|
C | T | 1 | a0001c0006 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.1239G>A | p.Ala413Ala | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1500/3172 | 1239/1803 | 413/600 | chr19 | 16576591 | ||
| chr19:16576891
|
C | T | 1 | a0001c0005 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.939G>A | p.Pro313Pro | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1200/3172 | 939/1803 | 313/600 | chr19 | 16576891 | ||
| chr19:16576942
|
G | A | 1 | a0001c0009 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.888C>T | p.Ser296Ser | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1149/3172 | 888/1803 | 296/600 | chr19 | 16576942 | ||
| chr19:16577059
|
G | A | 1 | a0001c0002 | 12 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
synonymous_variant | LOW | c.771C>T | p.Asp257Asp | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1032/3172 | 771/1803 | 257/600 | chr19 | 16577059 | ||
| chr19:16577647
|
G | A | 1 | a0001c0003 | 2 | HG00738.hp1 HG03927.hp2 |
synonymous_variant | LOW | c.183C>T | p.Arg61Arg | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 444/3172 | 183/1803 | 61/600 | chr19 | 16577647 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16574921
|
GT | G | 4 | a0001c0001t0002a0001c0001t0005a0001c0005t0003others(1): Show | 14 | HG01070.hp2 HG01071.hp2 HG01943.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1105delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1105 | chr19 | 16574921 | |||||
| chr19:16575124
|
C | T | 1 | a0001c0001t0007 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 903 | chr19 | 16575124 | |||||
| chr19:16575128
|
G | A | 1 | a0001c0001t0008 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 899 | chr19 | 16575128 | |||||
| chr19:16575521
|
G | T | 1 | a0001c0001t0006 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 506 | chr19 | 16575521 | |||||
| chr19:16575634
|
A | G | 1 | a0001c0001t0005 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 393 | chr19 | 16575634 | |||||
| chr19:16575809
|
G | A | 1 | a0001c0001t0009 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 218 | chr19 | 16575809 | |||||
| chr19:16575894
|
C | T | 1 | a0001c0001t0004 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 133 | chr19 | 16575894 | |||||
| chr19:16576025
|
G | T | 1 | a0001c0005t0003 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 2 | chr19 | 16576025 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16577714
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.148-32G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16577714 | ||||||
| chr19:16577943
|
C | A | 1 | a0001c0001t0001g0135 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.148-261G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16577943 | ||||||
| chr19:16578017
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147+318C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578017 | ||||||
| chr19:16578069
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+266A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578069 | ||||||
| chr19:16578270
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.147+65G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578270 | ||||||
| chr19:16578291
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+44G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578291 | ||||||
| chr19:16578429
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.73-20A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578429 | ||||||
| chr19:16578603
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | NA18991.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.73-194G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578603 | ||||||
| chr19:16578804
|
T | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-395A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578804 | ||||||
| chr19:16578828
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-419G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578828 | ||||||
| chr19:16578890
|
C | T | 1 | a0001c0001t0005g0216 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-481G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578890 | ||||||
| chr19:16578895
|
G | T | 1 | a0001c0001t0002g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-486C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578895 | ||||||
| chr19:16578929
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | NA18612.hp2 NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.73-520G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578929 | ||||||
| chr19:16579106
|
T | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-697A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579106 | ||||||
| chr19:16579162
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.73-753C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579162 | ||||||
| chr19:16579424
|
G | A | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-1015C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579424 | ||||||
| chr19:16579705
|
C | G | 1 | a0001c0001t0007g0148 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.73-1296G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579705 | ||||||
| chr19:16579964
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.73-1555T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579964 | ||||||
| chr19:16579991
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.73-1582G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579991 | ||||||
| chr19:16580002
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-1593G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580002 | ||||||
| chr19:16580202
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0182 | 2 | HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.73-1793C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580202 | ||||||
| chr19:16580215
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02451.hp1 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.73-1806C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580215 | ||||||
| chr19:16580493
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-2084G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580493 | ||||||
| chr19:16580541
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0053others(2): Show | 7 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-2132C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580541 | ||||||
| chr19:16580729
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.73-2320C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580729 | ||||||
| chr19:16580818
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.73-2409G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580818 | ||||||
| chr19:16580847
|
T | G | 1 | a0001c0009t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.73-2438A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580847 | ||||||
| chr19:16581170
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.73-2761C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581170 | ||||||
| chr19:16581214
|
TC | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.73-2806delG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581214 | ||||||
| chr19:16581283
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.73-2874T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581283 | ||||||
| chr19:16581441
|
C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-3032G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581441 | ||||||
| chr19:16581518
|
A | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-3109T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581518 | ||||||
| chr19:16581817
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-3408G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581817 | ||||||
| chr19:16581895
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-3486G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581895 | ||||||
| chr19:16581896
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.73-3487C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581896 | ||||||
| chr19:16581911
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-3502G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581911 | ||||||
| chr19:16581916
|
G | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-3507C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581916 | ||||||
| chr19:16582090
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.73-3681G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582090 | ||||||
| chr19:16582126
|
A | G | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-3717T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582126 | ||||||
| chr19:16582143
|
G | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0056others(7): Show | 14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-3734C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582143 | ||||||
| chr19:16582182
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.73-3773C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582182 | ||||||
| chr19:16582213
|
G | T | 1 | a0001c0003t0001g0023 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.73-3804C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582213 | ||||||
| chr19:16582297
|
A | AT | 29 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.73-3889dupA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582297 | ||||||
| chr19:16582383
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.73-3974C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582383 | ||||||
| chr19:16582447
|
C | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0184 | 2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.73-4038G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582447 | ||||||
| chr19:16582461
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | NA18612.hp2 NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.73-4052A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582461 | ||||||
| chr19:16582578
|
G | C | 1 | a0001c0001t0002g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.73-4169C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582578 | ||||||
| chr19:16582633
|
G | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-4224C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582633 | ||||||
| chr19:16582639
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.73-4230G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582639 | ||||||
| chr19:16582701
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-4292C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582701 | ||||||
| chr19:16582794
|
T | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.73-4385A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582794 | ||||||
| chr19:16583006
|
T | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-4597A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583006 | ||||||
| chr19:16583079
|
G | A | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-4670C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583079 | ||||||
| chr19:16583095
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-4686G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583095 | ||||||
| chr19:16583283
|
T | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(25): Show | 35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-4874A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583283 | ||||||
| chr19:16583389
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.73-4980G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583389 | ||||||
| chr19:16583475
|
G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(32): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5066C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583475 | ||||||
| chr19:16583584
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-5175G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583584 | ||||||
| chr19:16583678
|
G | GCAGGTCC others(4): Show |
1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-5280_73-5270dup others(11): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583678 | ||||||
| chr19:16583701
|
T | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(25): Show | 35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-5292A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583701 | ||||||
| chr19:16583737
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-5328G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583737 | ||||||
| chr19:16583799
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(76): Show | 95 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.73-5390A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583799 | ||||||
| chr19:16583888
|
C | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-5479G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583888 | ||||||
| chr19:16584097
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(25): Show | 35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-5688T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584097 | ||||||
| chr19:16584168
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0050 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.73-5759C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584168 | ||||||
| chr19:16584287
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-5878T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584287 | ||||||
| chr19:16584300
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0133 | 3 | NA19002.hp1 NA19074.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.73-5891G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584300 | ||||||
| chr19:16584300
|
C | T | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-5891G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584300 | ||||||
| chr19:16584301
|
C | A | 12 | a0001c0001t0001g0107a0001c0002t0001g0015a0001c0002t0001g0096others(9): Show | 13 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-5892G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584301 | ||||||
| chr19:16584302
|
C | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-5893G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584302 | ||||||
| chr19:16584303
|
CG | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(13): Show | 23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-5895delC | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584303 | ||||||
| chr19:16584304
|
G | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0006g0078others(1): Show | 4 | HG00673.hp1 HG02280.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-5895C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584304 | ||||||
| chr19:16584306
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.73-5897G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584306 | ||||||
| chr19:16584311
|
C | CA | 42 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(39): Show | 47 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.73-5903dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584311 | ||||||
| chr19:16584426
|
G | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-6017C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584426 | ||||||
| chr19:16584445
|
T | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-6036A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584445 | ||||||
| chr19:16584470
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.73-6061C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584470 | ||||||
| chr19:16585070
|
T | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.73-6661A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585070 | ||||||
| chr19:16585256
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.73-6847C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585256 | ||||||
| chr19:16585288
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(10): Show | 20 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.73-6879C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585288 | ||||||
| chr19:16585439
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-7030C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585439 | ||||||
| chr19:16585710
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-7301C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585710 | ||||||
| chr19:16585735
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(13): Show | 23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-7326G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585735 | ||||||
| chr19:16585763
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028 | 4 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-7354A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585763 | ||||||
| chr19:16585858
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.73-7449T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585858 | ||||||
| chr19:16585907
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.73-7498G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585907 | ||||||
| chr19:16585909
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.73-7500G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585909 | ||||||
| chr19:16586015
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-7606G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586015 | ||||||
| chr19:16586265
|
A | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-7856T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586265 | ||||||
| chr19:16586279
|
G | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-7870C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586279 | ||||||
| chr19:16586432
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.73-8023G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586432 | ||||||
| chr19:16586481
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0088 | 2 | HG00673.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.73-8072G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586481 | ||||||
| chr19:16586539
|
C | T | 1 | a0001c0001t0004g0197 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.73-8130G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586539 | ||||||
| chr19:16586653
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.73-8244G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586653 | ||||||
| chr19:16586688
|
G | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(32): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-8279C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586688 | ||||||
| chr19:16586897
|
T | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.73-8488A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586897 | ||||||
| chr19:16586913
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.73-8504A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586913 | ||||||
| chr19:16587023
|
A | C | 1 | a0001c0001t0001g0022 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.73-8614T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587023 | ||||||
| chr19:16587093
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.73-8684C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587093 | ||||||
| chr19:16587095
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(19): Show | 26 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.73-8686C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587095 | ||||||
| chr19:16587119
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0038 | 4 | HG01256.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-8710G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587119 | ||||||
| chr19:16587764
|
T | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-9355A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587764 | ||||||
| chr19:16587805
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-9396T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587805 | ||||||
| chr19:16587914
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.73-9505G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587914 | ||||||
| chr19:16588120
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-9711G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588120 | ||||||
| chr19:16588159
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.73-9750C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588159 | ||||||
| chr19:16588320
|
T | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-9911A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588320 | ||||||
| chr19:16588513
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.73-10104C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588513 | ||||||
| chr19:16588529
|
G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(32): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-10120C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588529 | ||||||
| chr19:16588532
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73-10123G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588532 | ||||||
| chr19:16588804
|
C | T | 1 | a0001c0003t0001g0023 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.73-10395G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588804 | ||||||
| chr19:16588809
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-10400G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588809 | ||||||
| chr19:16588875
|
G | A | 21 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0212others(18): Show | 22 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-10466C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588875 | ||||||
| chr19:16589002
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(56): Show | 75 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.73-10593G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589002 | ||||||
| chr19:16589041
|
C | G | 23 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(20): Show | 24 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.73-10632G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589041 | ||||||
| chr19:16589081
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-10672C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589081 | ||||||
| chr19:16589209
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-10800C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589209 | ||||||
| chr19:16589216
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.73-10807C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589216 | ||||||
| chr19:16589240
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 157 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.73-10831T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589240 | ||||||
| chr19:16589441
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.73-11032C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589441 | ||||||
| chr19:16589933
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.73-11524G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589933 | ||||||
| chr19:16590076
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-11667G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590076 | ||||||
| chr19:16590331
|
C | A | 5 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0212others(2): Show | 5 | HG02280.hp2 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-11922G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590331 | ||||||
| chr19:16590429
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(32): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-12020G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590429 | ||||||
| chr19:16590645
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026others(1): Show | 4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-12236C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590645 | ||||||
| chr19:16590768
|
C | T | 9 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0212others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.73-12359G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590768 | ||||||
| chr19:16590776
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-12367T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590776 | ||||||
| chr19:16590822
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-12413C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590822 | ||||||
| chr19:16590899
|
G | GCACC | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-12491_73-12490i others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590899 | ||||||
| chr19:16590925
|
A | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-12516T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590925 | ||||||
| chr19:16591043
|
AAAATAAA others(14): Show |
A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-12655_73-12635d others(23): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591043 | ||||||
| chr19:16591048
|
A | AAAAT | 4 | a0001c0001t0001g0094a0001c0001t0001g0163a0001c0002t0001g0100others(1): Show | 4 | HG02015.hp1 HG02109.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-12643_73-12640d others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | ||||||
| chr19:16591048
|
AAAAT | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 86 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.73-12643_73-12640d others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | ||||||
| chr19:16591048
|
AAAATAAA others(1): Show |
A | 53 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(50): Show | 59 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.73-12647_73-12640d others(10): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | ||||||
| chr19:16591048
|
AAAATAAA others(5): Show |
A | 19 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0047others(16): Show | 26 | HG01070.hp1 HG01192.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.73-12651_73-12640d others(14): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | ||||||
| chr19:16591048
|
AAAATAAA others(9): Show |
A | 9 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0061others(6): Show | 10 | HG00609.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-12655_73-12640d others(18): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | ||||||
| chr19:16591048
|
AAAATAAA others(13): Show |
A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-12659_73-12640d others(22): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | ||||||
| chr19:16591053
|
AAATAAAT others(4): Show |
A | 1 | a0001c0001t0001g0114 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.73-12655_73-12645d others(13): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591053 | ||||||
| chr19:16591142
|
A | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-12733T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591142 | ||||||
| chr19:16591295
|
C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-12886G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591295 | ||||||
| chr19:16591321
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.73-12912C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591321 | ||||||
| chr19:16591352
|
ATG | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-12945_73-12944d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591352 | ||||||
| chr19:16591459
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.73-13050A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591459 | ||||||
| chr19:16591659
|
C | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0219 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.73-13250G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591659 | ||||||
| chr19:16591992
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73-13583G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591992 | ||||||
| chr19:16592209
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.73-13800A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592209 | ||||||
| chr19:16592541
|
C | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(24): Show | 34 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-14132G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592541 | ||||||
| chr19:16592541
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-14132G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592541 | ||||||
| chr19:16592542
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-14133C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592542 | ||||||
| chr19:16592626
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-14217C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592626 | ||||||
| chr19:16592877
|
C | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0056others(7): Show | 14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-14468G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592877 | ||||||
| chr19:16592999
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(13): Show | 23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-14590G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592999 | ||||||
| chr19:16593025
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.73-14616C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593025 | ||||||
| chr19:16593099
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-14690T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593099 | ||||||
| chr19:16593409
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-15000T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593409 | ||||||
| chr19:16593520
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-15111C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593520 | ||||||
| chr19:16593770
|
A | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-15361T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593770 | ||||||
| chr19:16593928
|
C | T | 1 | a0001c0001t0008g0178 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.73-15519G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593928 | ||||||
| chr19:16593970
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.73-15561T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593970 | ||||||
| chr19:16594031
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.73-15622C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16594031 | ||||||
| chr19:16594532
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.73-16123A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16594532 | ||||||
| chr19:16594896
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-16487C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16594896 | ||||||
| chr19:16595201
|
G | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-16792C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595201 | ||||||
| chr19:16595327
|
G | A | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-16918C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595327 | ||||||
| chr19:16595386
|
T | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-16977A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595386 | ||||||
| chr19:16595437
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0056others(7): Show | 14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-17028G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595437 | ||||||
| chr19:16595485
|
T | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-17076A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595485 | ||||||
| chr19:16595621
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.73-17212T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595621 | ||||||
| chr19:16596248
|
T | A | 1 | a0001c0001t0001g0032 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.73-17839A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596248 | ||||||
| chr19:16596294
|
C | G | 1 | a0001c0001t0009g0186 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.73-17885G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596294 | ||||||
| chr19:16596857
|
G | GC | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-18449dupG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596857 | ||||||
| chr19:16596873
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(13): Show | 23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-18464G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596873 | ||||||
| chr19:16596991
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.73-18582T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596991 | ||||||
| chr19:16597087
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.73-18678G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597087 | ||||||
| chr19:16597205
|
T | TA | 16 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(13): Show | 23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-18797dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597205 | ||||||
| chr19:16597259
|
A | G | 1 | a0001c0001t0008g0178 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.73-18850T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597259 | ||||||
| chr19:16597369
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.73-18960G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597369 | ||||||
| chr19:16597622
|
G | A | 1 | a0003c0007t0001g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-19213C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597622 | ||||||
| chr19:16597623
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.73-19214G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597623 | ||||||
| chr19:16597774
|
G | A | 2 | a0001c0002t0001g0100a0001c0002t0001g0101 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.73-19365C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597774 | ||||||
| chr19:16597810
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(13): Show | 23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-19401G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597810 | ||||||
| chr19:16597923
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.73-19514A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597923 | ||||||
| chr19:16598117
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 34 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-19708G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598117 | ||||||
| chr19:16598193
|
C | T | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-19784G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598193 | ||||||
| chr19:16598200
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.73-19791C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598200 | ||||||
| chr19:16598229
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.73-19820G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598229 | ||||||
| chr19:16598336
|
C | CA | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.73-19928dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598336 | ||||||
| chr19:16598336
|
C | CAA | 45 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 51 | HG00621.hp1 HG00741.hp1 HG01256.hp1 others(48): Show |
intron_variant | MODIFIER | c.73-19929_73-19928d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598336 | ||||||
| chr19:16598336
|
C | CAAA | 7 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0042others(4): Show | 7 | HG01167.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-19930_73-19928d others(5): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598336 | ||||||
| chr19:16598481
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 8 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-20072A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598481 | ||||||
| chr19:16598680
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-20271G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598680 | ||||||
| chr19:16598804
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.73-20395C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598804 | ||||||
| chr19:16598852
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.73-20443A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598852 | ||||||
| chr19:16598919
|
T | TA | 26 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0020others(23): Show | 35 | HG00609.hp2 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-20511dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598919 | ||||||
| chr19:16598935
|
C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-20526G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598935 | ||||||
| chr19:16599114
|
G | C | 2 | a0001c0002t0001g0100a0001c0002t0001g0101 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.73-20705C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599114 | ||||||
| chr19:16599197
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-20788G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599197 | ||||||
| chr19:16599211
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.73-20802G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599211 | ||||||
| chr19:16599759
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.73-21350C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599759 | ||||||
| chr19:16599872
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-21463T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599872 | ||||||
| chr19:16599951
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.73-21542T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599951 | ||||||
| chr19:16600183
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 8 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-21774T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600183 | ||||||
| chr19:16600266
|
T | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-21857A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600266 | ||||||
| chr19:16600454
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.73-22045G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600454 | ||||||
| chr19:16600461
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.73-22052T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600461 | ||||||
| chr19:16600984
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.73-22575G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600984 | ||||||
| chr19:16601136
|
G | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-22727C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601136 | ||||||
| chr19:16601159
|
C | CT | 51 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(48): Show | 63 | HG00621.hp1 HG01192.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.73-22751dupA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601159 | ||||||
| chr19:16601299
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-22890C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601299 | ||||||
| chr19:16601419
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-23010A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601419 | ||||||
| chr19:16601516
|
C | T | 1 | a0004c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73-23107G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601516 | ||||||
| chr19:16601523
|
G | A | 1 | a0001c0009t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.73-23114C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601523 | ||||||
| chr19:16601652
|
C | T | 1 | a0001c0001t0001g0017 | 2 | NA19002.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.73-23243G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601652 | ||||||
| chr19:16601657
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-23248T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601657 | ||||||
| chr19:16601780
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028 | 4 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-23371G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601780 | ||||||
| chr19:16601800
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.73-23391G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601800 | ||||||
| chr19:16601889
|
C | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0149others(6): Show | 11 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-23480G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601889 | ||||||
| chr19:16602091
|
G | A | 1 | a0001c0001t0005g0216 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-23682C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602091 | ||||||
| chr19:16602137
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.73-23728T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602137 | ||||||
| chr19:16602162
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.73-23753A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602162 | ||||||
| chr19:16602210
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.73-23801T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602210 | ||||||
| chr19:16602270
|
G | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026others(1): Show | 4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-23861C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602270 | ||||||
| chr19:16602307
|
C | G | 1 | a0001c0001t0001g0011 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.73-23898G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602307 | ||||||
| chr19:16602459
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.73-24050C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602459 | ||||||
| chr19:16602521
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 34 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-24112G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602521 | ||||||
| chr19:16602744
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-24335G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602744 | ||||||
| chr19:16602969
|
A | C | 1 | a0004c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73-24560T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602969 | ||||||
| chr19:16603034
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-24625G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603034 | ||||||
| chr19:16603085
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.73-24676G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603085 | ||||||
| chr19:16603159
|
A | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(25): Show | 35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.72+24713T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603159 | ||||||
| chr19:16603470
|
A | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+24402T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603470 | ||||||
| chr19:16603471
|
A | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+24401T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603471 | ||||||
| chr19:16603657
|
T | C | 2 | a0001c0002t0001g0103a0001c0002t0001g0104 | 2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72+24215A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603657 | ||||||
| chr19:16603791
|
T | TCTGGCTC others(7): Show |
1 | a0001c0001t0002g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.72+24067_72+24080d others(16): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603791 | ||||||
| chr19:16604011
|
T | A | 2 | a0001c0001t0001g0107a0004c0008t0001g0092 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.72+23861A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604011 | ||||||
| chr19:16604155
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(25): Show | 35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.72+23717A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604155 | ||||||
| chr19:16604323
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.72+23549A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604323 | ||||||
| chr19:16604420
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028 | 4 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+23452G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604420 | ||||||
| chr19:16604461
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.72+23411C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604461 | ||||||
| chr19:16604486
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.72+23386G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604486 | ||||||
| chr19:16604647
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.72+23225A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604647 | ||||||
| chr19:16604795
|
C | A | 8 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0215others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+23077G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604795 | ||||||
| chr19:16604812
|
C | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.72+23060G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604812 | ||||||
| chr19:16604823
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+23049G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604823 | ||||||
| chr19:16604887
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+22985T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604887 | ||||||
| chr19:16605047
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.72+22825C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605047 | ||||||
| chr19:16605080
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.72+22792T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605080 | ||||||
| chr19:16605148
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.72+22724G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605148 | ||||||
| chr19:16605199
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0191 | 2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.72+22673A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605199 | ||||||
| chr19:16605229
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+22643G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605229 | ||||||
| chr19:16605254
|
T | C | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+22618A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605254 | ||||||
| chr19:16605314
|
G | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(10): Show | 20 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.72+22558C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605314 | ||||||
| chr19:16605536
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+22336C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605536 | ||||||
| chr19:16605629
|
T | G | 1 | a0001c0001t0002g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.72+22243A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605629 | ||||||
| chr19:16605769
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+22103C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605769 | ||||||
| chr19:16606030
|
G | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG01934.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.72+21842C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606030 | ||||||
| chr19:16606034
|
G | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+21838C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606034 | ||||||
| chr19:16606092
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+21780G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606092 | ||||||
| chr19:16606421
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+21451C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606421 | ||||||
| chr19:16606661
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.72+21211A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606661 | ||||||
| chr19:16606732
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+21140T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606732 | ||||||
| chr19:16606824
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.72+21048A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606824 | ||||||
| chr19:16606864
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+21008T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606864 | ||||||
| chr19:16606875
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.72+20997C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606875 | ||||||
| chr19:16606882
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG00544.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.72+20990G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606882 | ||||||
| chr19:16606943
|
A | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG00639.hp2 HG01168.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+20929T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606943 | ||||||
| chr19:16607128
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0056others(7): Show | 14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.72+20744A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607128 | ||||||
| chr19:16607191
|
T | TA | 29 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.72+20680dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607191 | ||||||
| chr19:16607261
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.72+20611G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607261 | ||||||
| chr19:16607375
|
G | GA | 11 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(8): Show | 12 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+20496dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607375 | ||||||
| chr19:16607375
|
GA | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0057others(5): Show | 11 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+20496delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607375 | ||||||
| chr19:16607376
|
A | G | 7 | a0001c0001t0001g0133a0001c0001t0001g0205a0001c0001t0002g0098others(4): Show | 7 | HG00741.hp2 HG02280.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+20496T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607376 | ||||||
| chr19:16607402
|
T | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+20470A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607402 | ||||||
| chr19:16607448
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.72+20424G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607448 | ||||||
| chr19:16607698
|
C | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+20174G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607698 | ||||||
| chr19:16607730
|
A | AT | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+20141dupA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607730 | ||||||
| chr19:16607751
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+20121G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607751 | ||||||
| chr19:16607798
|
C | A | 1 | a0001c0001t0001g0141 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.72+20074G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607798 | ||||||
| chr19:16607806
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.72+20066C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607806 | ||||||
| chr19:16607871
|
C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+20001G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607871 | ||||||
| chr19:16607902
|
A | G | 5 | a0001c0001t0001g0137a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+19970T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607902 | ||||||
| chr19:16608185
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.72+19687G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608185 | ||||||
| chr19:16608251
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0163others(5): Show | 10 | HG00609.hp2 HG00621.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+19621A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608251 | ||||||
| chr19:16608644
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+19228A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608644 | ||||||
| chr19:16608705
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.72+19167C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608705 | ||||||
| chr19:16608958
|
T | C | 1 | a0001c0002t0001g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.72+18914A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608958 | ||||||
| chr19:16609023
|
G | A | 1 | a0001c0009t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72+18849C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609023 | ||||||
| chr19:16609193
|
T | C | 1 | a0001c0003t0001g0023 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.72+18679A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609193 | ||||||
| chr19:16609198
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+18674C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609198 | ||||||
| chr19:16609215
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(29): Show | 40 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.72+18657T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609215 | ||||||
| chr19:16609236
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+18636G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609236 | ||||||
| chr19:16609294
|
A | C | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.72+18578T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609294 | ||||||
| chr19:16609311
|
C | CA | 57 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(54): Show | 64 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.72+18560dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | ||||||
| chr19:16609311
|
C | CAA | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(13): Show | 19 | HG00621.hp1 HG01884.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.72+18559_72+18560d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | ||||||
| chr19:16609311
|
CA | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0168a0001c0001t0001g0172others(3): Show | 6 | HG01975.hp2 HG03098.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+18560delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | ||||||
| chr19:16609311
|
CAAAA | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(10): Show | 20 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.72+18557_72+18560d others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | ||||||
| chr19:16609336
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0086 | 2 | HG04115.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.72+18535_72+18536i others(18): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609336 | ||||||
| chr19:16609336
|
A | AAAAAAAA others(8): Show |
8 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(5): Show | 8 | HG00099.hp1 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+18535_72+18536i others(17): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609336 | ||||||
| chr19:16609336
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0006t0001g0082 | 3 | HG00673.hp1 HG02071.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.72+18535_72+18536i others(16): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609336 | ||||||
| chr19:16609418
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.72+18454C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609418 | ||||||
| chr19:16609450
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+18422G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609450 | ||||||
| chr19:16609563
|
TTCTTTTC others(519): Show |
T | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+17783_72+18308d others(2): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609563 | ||||||
| chr19:16609567
|
T | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+18305A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609567 | ||||||
| chr19:16609826
|
T | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+18046A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609826 | ||||||
| chr19:16609827
|
T | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+18045A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609827 | ||||||
| chr19:16609941
|
T | TA | 12 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.72+17930dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | ||||||
| chr19:16609941
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.72+17921_72+17930d others(12): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | ||||||
| chr19:16609941
|
T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0062a0001c0001t0006g0078 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.72+17920_72+17930d others(13): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | ||||||
| chr19:16609941
|
TA | T | 46 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0016others(43): Show | 52 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.72+17930delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | ||||||
| chr19:16609941
|
TAA | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(6): Show | 16 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.72+17929_72+17930d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | ||||||
| chr19:16609941
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.72+17919_72+17930d others(14): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | ||||||
| chr19:16610039
|
T | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(35): Show | 49 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.72+17833A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610039 | ||||||
| chr19:16610082
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.72+17790G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610082 | ||||||
| chr19:16610089
|
G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(32): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+17783C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610089 | ||||||
| chr19:16610188
|
A | G | 9 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0212others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+17684T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610188 | ||||||
| chr19:16610305
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+17567T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610305 | ||||||
| chr19:16610317
|
A | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+17555T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610317 | ||||||
| chr19:16610340
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0074 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+17532C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610340 | ||||||
| chr19:16610372
|
T | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+17500A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610372 | ||||||
| chr19:16610394
|
CT | C | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0087others(5): Show | 8 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+17477delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610394 | ||||||
| chr19:16610417
|
A | AG | 2 | a0001c0001t0001g0013a0001c0001t0001g0074 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+17454dupC | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610417 | ||||||
| chr19:16610429
|
G | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+17443C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610429 | ||||||
| chr19:16610523
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.72+17349G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610523 | ||||||
| chr19:16610570
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.72+17302A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610570 | ||||||
| chr19:16610870
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+17002C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610870 | ||||||
| chr19:16610987
|
A | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 9 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+16885T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610987 | ||||||
| chr19:16611030
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.72+16842C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611030 | ||||||
| chr19:16611196
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0074a0001c0001t0001g0075 | 4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+16676C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611196 | ||||||
| chr19:16611258
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.72+16614C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611258 | ||||||
| chr19:16611395
|
TC | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0074 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+16476delG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611395 | ||||||
| chr19:16611474
|
T | C | 14 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 14 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.72+16398A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611474 | ||||||
| chr19:16611497
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.72+16375G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611497 | ||||||
| chr19:16611537
|
T | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026others(1): Show | 4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+16335A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611537 | ||||||
| chr19:16611939
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+15933G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611939 | ||||||
| chr19:16612129
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72+15743G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612129 | ||||||
| chr19:16612137
|
C | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+15735G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612137 | ||||||
| chr19:16612290
|
TG | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG00639.hp2 HG01168.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+15581delC | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612290 | ||||||
| chr19:16612663
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.72+15209G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612663 | ||||||
| chr19:16612690
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.72+15182A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612690 | ||||||
| chr19:16612720
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.72+15152C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612720 | ||||||
| chr19:16612729
|
G | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+15143C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612729 | ||||||
| chr19:16612772
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 44 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.72+15100T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612772 | ||||||
| chr19:16612818
|
C | G | 1 | a0001c0001t0002g0217 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.72+15054G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612818 | ||||||
| chr19:16612834
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.72+15038A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612834 | ||||||
| chr19:16612989
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72+14883G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612989 | ||||||
| chr19:16613182
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 44 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.72+14690G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613182 | ||||||
| chr19:16613478
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 34 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.72+14394G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613478 | ||||||
| chr19:16613503
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(32): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+14369G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613503 | ||||||
| chr19:16613593
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.72+14279C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613593 | ||||||
| chr19:16613616
|
G | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+14256C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613616 | ||||||
| chr19:16614023
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0074 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+13849C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614023 | ||||||
| chr19:16614057
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.72+13815G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614057 | ||||||
| chr19:16614270
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+13602C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614270 | ||||||
| chr19:16614344
|
A | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026others(1): Show | 4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+13528T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614344 | ||||||
| chr19:16614376
|
A | C | 2 | a0001c0002t0001g0100a0001c0002t0001g0101 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.72+13496T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614376 | ||||||
| chr19:16614398
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72+13474C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614398 | ||||||
| chr19:16614404
|
C | A | 9 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0212others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+13468G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614404 | ||||||
| chr19:16614558
|
G | T | 1 | a0004c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+13314C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614558 | ||||||
| chr19:16614559
|
G | C | 1 | a0001c0001t0001g0035 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.72+13313C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614559 | ||||||
| chr19:16614652
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+13220C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614652 | ||||||
| chr19:16614655
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.72+13217C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614655 | ||||||
| chr19:16614700
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.72+13172C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614700 | ||||||
| chr19:16614753
|
C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+13119G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614753 | ||||||
| chr19:16614841
|
C | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+13031G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614841 | ||||||
| chr19:16615544
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.72+12328G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615544 | ||||||
| chr19:16615597
|
T | A | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.72+12275A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615597 | ||||||
| chr19:16615703
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.72+12169T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615703 | ||||||
| chr19:16615753
|
GA | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(33): Show | 42 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.72+12118delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615753 | ||||||
| chr19:16616064
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.72+11808C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616064 | ||||||
| chr19:16616100
|
G | C | 1 | a0001c0002t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.72+11772C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616100 | ||||||
| chr19:16616178
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.72+11694C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616178 | ||||||
| chr19:16616207
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(8): Show | 12 | HG01891.hp1 HG01934.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+11665C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616207 | ||||||
| chr19:16616242
|
AT | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0053others(2): Show | 7 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+11629delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616242 | ||||||
| chr19:16616318
|
A | G | 40 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 45 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.72+11554T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616318 | ||||||
| chr19:16616380
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.72+11492A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616380 | ||||||
| chr19:16616441
|
A | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02015.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.72+11431T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616441 | ||||||
| chr19:16616548
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+11324G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616548 | ||||||
| chr19:16616870
|
C | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+11002G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616870 | ||||||
| chr19:16617086
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+10786G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617086 | ||||||
| chr19:16617157
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72+10715T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617157 | ||||||
| chr19:16617229
|
A | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.72+10643T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617229 | ||||||
| chr19:16617230
|
G | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.72+10642C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617230 | ||||||
| chr19:16617343
|
T | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+10529A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617343 | ||||||
| chr19:16617531
|
A | G | 5 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0212others(2): Show | 5 | HG02280.hp2 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+10341T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617531 | ||||||
| chr19:16617569
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.72+10303T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617569 | ||||||
| chr19:16617572
|
T | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0116others(11): Show | 16 | HG00408.hp1 HG00423.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+10300A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617572 | ||||||
| chr19:16617785
|
T | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+10087A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617785 | ||||||
| chr19:16617808
|
GA | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 129 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.72+10063delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617808 | ||||||
| chr19:16617911
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72+9961C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617911 | ||||||
| chr19:16617922
|
G | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.72+9950C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617922 | ||||||
| chr19:16618040
|
CT | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0061others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+9831delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618040 | ||||||
| chr19:16618243
|
A | G | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00544.hp1 HG02083.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+9629T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618243 | ||||||
| chr19:16618392
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.72+9480G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618392 | ||||||
| chr19:16618597
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.72+9275T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618597 | ||||||
| chr19:16618685
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.72+9187A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618685 | ||||||
| chr19:16618704
|
C | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0030others(11): Show | 16 | HG00621.hp1 HG01256.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+9168G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618704 | ||||||
| chr19:16618923
|
G | A | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219 | 3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.72+8949C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618923 | ||||||
| chr19:16618994
|
G | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+8878C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618994 | ||||||
| chr19:16619008
|
GGGCC | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0069others(5): Show | 14 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.72+8860_72+8863del others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619008 | ||||||
| chr19:16619015
|
C | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+8857G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619015 | ||||||
| chr19:16619019
|
A | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0069others(5): Show | 14 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.72+8853T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619019 | ||||||
| chr19:16619046
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.72+8826G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619046 | ||||||
| chr19:16619265
|
G | A | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+8607C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619265 | ||||||
| chr19:16619324
|
T | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(34): Show | 43 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.72+8548A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619324 | ||||||
| chr19:16619327
|
A | C | 1 | a0003c0007t0001g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+8545T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619327 | ||||||
| chr19:16619349
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 8 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+8523G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619349 | ||||||
| chr19:16619385
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 136 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.72+8487A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619385 | ||||||
| chr19:16619404
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0116a0001c0001t0001g0117 | 4 | HG03017.hp1 HG03927.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+8468G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619404 | ||||||
| chr19:16619467
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.72+8405C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619467 | ||||||
| chr19:16619758
|
G | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+8114C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619758 | ||||||
| chr19:16619967
|
C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+7905G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619967 | ||||||
| chr19:16620008
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.72+7864A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620008 | ||||||
| chr19:16620022
|
T | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+7850A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620022 | ||||||
| chr19:16620300
|
C | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(9): Show | 12 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+7572G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620300 | ||||||
| chr19:16620334
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 5 | HG00408.hp1 NA18990.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+7538C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620334 | ||||||
| chr19:16620591
|
A | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG00544.hp2 NA18966.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+7281T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620591 | ||||||
| chr19:16620656
|
T | C | 1 | a0003c0007t0001g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+7216A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620656 | ||||||
| chr19:16620909
|
C | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG00639.hp2 HG01168.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+6963G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620909 | ||||||
| chr19:16621043
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0222 | 2 | NA19006.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.72+6829T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621043 | ||||||
| chr19:16621104
|
G | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+6768C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621104 | ||||||
| chr19:16621133
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.72+6739C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621133 | ||||||
| chr19:16621223
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.72+6649A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621223 | ||||||
| chr19:16621237
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.72+6635T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621237 | ||||||
| chr19:16621240
|
C | T | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+6632G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621240 | ||||||
| chr19:16621249
|
T | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+6623A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621249 | ||||||
| chr19:16621517
|
A | G | 1 | a0001c0009t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72+6355T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621517 | ||||||
| chr19:16621551
|
T | C | 1 | a0003c0007t0001g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+6321A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621551 | ||||||
| chr19:16621872
|
C | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0026 | 3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.72+6000G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621872 | ||||||
| chr19:16622291
|
G | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.72+5581C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622291 | ||||||
| chr19:16622323
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0067others(8): Show | 18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+5549C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622323 | ||||||
| chr19:16622574
|
G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(32): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+5298C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622574 | ||||||
| chr19:16622890
|
C | A | 8 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0215others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+4982G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622890 | ||||||
| chr19:16623053
|
C | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+4819G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623053 | ||||||
| chr19:16623399
|
T | C | 2 | a0001c0001t0001g0107a0004c0008t0001g0092 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.72+4473A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623399 | ||||||
| chr19:16623522
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.72+4350G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623522 | ||||||
| chr19:16623684
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.72+4188C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623684 | ||||||
| chr19:16623759
|
C | T | 1 | a0003c0007t0001g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+4113G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623759 | ||||||
| chr19:16623762
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG00609.hp1 HG02040.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+4110G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623762 | ||||||
| chr19:16624124
|
AC | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+3747delG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624124 | ||||||
| chr19:16624125
|
C | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0065others(13): Show | 23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.72+3747G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624125 | ||||||
| chr19:16624235
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.72+3637C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624235 | ||||||
| chr19:16624583
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.72+3289G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624583 | ||||||
| chr19:16624661
|
T | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+3211A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624661 | ||||||
| chr19:16624666
|
A | G | 2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.72+3206T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624666 | ||||||
| chr19:16624811
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.72+3061A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624811 | ||||||
| chr19:16624977
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+2895G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624977 | ||||||
| chr19:16625018
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.72+2854G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625018 | ||||||
| chr19:16625096
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+2776G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625096 | ||||||
| chr19:16625196
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+2676C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625196 | ||||||
| chr19:16625281
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 43 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.72+2591T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625281 | ||||||
| chr19:16625355
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.72+2517C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625355 | ||||||
| chr19:16625415
|
G | A | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+2457C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625415 | ||||||
| chr19:16625542
|
GT | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0068others(12): Show | 22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+2329delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625542 | ||||||
| chr19:16625555
|
TC | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+2316delG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625555 | ||||||
| chr19:16626018
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.72+1854A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626018 | ||||||
| chr19:16626326
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01071.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.72+1546A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626326 | ||||||
| chr19:16626418
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.72+1454A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626418 | ||||||
| chr19:16626565
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+1307G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626565 | ||||||
| chr19:16626644
|
G | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+1228C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626644 | ||||||
| chr19:16626940
|
A | AAC | 14 | a0001c0001t0001g0107a0001c0001t0002g0026a0001c0001t0002g0098others(11): Show | 15 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.72+930_72+931dupGT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626940 | ||||||
| chr19:16626961
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG01071.hp1 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.72+911C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626961 | ||||||
| chr19:16627024
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+848A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627024 | ||||||
| chr19:16627241
|
T | C | 1 | a0004c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+631A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627241 | ||||||
| chr19:16627362
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.72+510C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627362 | ||||||
| chr19:16627543
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+329C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627543 | ||||||
| chr19:16627558
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(78): Show | 98 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.72+314T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627558 | ||||||
| chr19:16627690
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+182G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627690 |