geneid | 9439 |
---|---|
ensemblid | ENSG00000112282.18 |
hgncid | 2372 |
symbol | MED23 |
name | mediator complex subunit 23 |
refseq_nuc | NM_004830.4 |
refseq_prot | NP_004821.2 |
ensembl_nuc | ENST00000368068.8 |
ensembl_prot | ENSP00000357047.3 |
mane_status | MANE Select |
chr | chr6 |
start | 131586732 |
end | 131628242 |
strand | - |
ver | v1.2 |
region | chr6:131586732-131628242 |
region5000 | chr6:131581732-131633242 |
regionname0 | MED23_chr6_131586732_131628242 |
regionname5000 | MED23_chr6_131581732_131633242 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1368 | 317 | 88 | 50 | 135 | 12 | 30 | 111 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0002 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0003 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0004 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4107 | 311 | 86 | 49 | 132 | 12 | 30 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
c0002 | 0/0 | 4107 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
c0003 | 0/0 | 4107 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
c0004 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
c0005 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
c0006 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
c0007 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
c0008 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1141 | 292 | 80 | 49 | 123 | 12 | 26 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0002 | 0/0 | 1141 | 8 | 4 | 1 | 0 | 0 | 3 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0003 | 0/0 | 1141 | 6 | 6 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0004 | 0/0 | 1141 | 5 | 0 | 0 | 5 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0005 | 0/0 | 1141 | 4 | 0 | 0 | 4 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0006 | 0/0 | 1141 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0007 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0008 | 0/0 | 1141 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
t0009 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 20 | 1 | 4 | 10 | 0 | 4 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0002 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0004 | 0/0 | 8 | 0 | 3 | 1 | 0 | 4 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0007 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0008 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4107 | 311 | 86 | 49 | 132 | 12 | 30 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0002 | 0/0 | 4107 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0003 | 0/0 | 4107 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0004 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0008 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0002c0006 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0003c0007 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0004c0005 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5247 | 283 | 76 | 48 | 119 | 12 | 26 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0002 | 0/0 | 5247 | 8 | 4 | 1 | 0 | 0 | 3 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0003 | 0/0 | 5247 | 6 | 6 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0004 | 0/0 | 5247 | 5 | 0 | 0 | 5 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0005 | 0/0 | 5247 | 4 | 0 | 0 | 4 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0006 | 0/0 | 5247 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0007 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0008 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0001t0009 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0002t0001 | 0/0 | 5247 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0003t0001 | 0/0 | 5247 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0004t0001 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0001c0008t0001 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0002c0006t0001 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0003c0007t0001 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
a0004c0005t0001 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | copy fasta | chr6 | 131581732 | 131633242 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 20 | 1 | 4 | 10 | 0 | 4 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0002 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 1 | 0 | 4 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0007 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0001c0008t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0002c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0003c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
a0004c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02622 | hp1 | a0002 | c0006 | t0001 | g0150 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02809 | hp1 | a0004 | c0005 | t0001 | g0078 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03834 | hp1 | a0001 | c0001 | t0008 | g0110 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18953 | hp1 | a0001 | c0001 | t0007 | g0168 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0194 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18991 | hp1 | a0003 | c0007 | t0001 | g0139 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19004 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19006 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19009 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19072 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19085 | hp1 | a0001 | c0008 | t0001 | g0187 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ASW | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0088 | REF | REF | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:131589503
|
T | G | 1 | a0003 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.3901A>C | p.Met1301Leu | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/29 | 4094/5247 | 3901/4107 | 1301/1368 | chr6 | 131589503 | ||
chr6:131590387
|
C | T | 1 | a0002 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3742G>A | p.Val1248Ile | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/29 | 3935/5247 | 3742/4107 | 1248/1368 | chr6 | 131590387 | ||
chr6:131590405
|
C | T | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.3724G>A | p.Glu1242Lys | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/29 | 3917/5247 | 3724/4107 | 1242/1368 | chr6 | 131590405 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:131587706
|
C | A | 1 | a0001c0002 | 2 | HG02258.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.4080G>T | p.Val1360Val | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 4273/5247 | 4080/4107 | 1360/1368 | chr6 | 131587706 | ||
chr6:131602378
|
G | A | 1 | a0001c0003 | 2 | HG01975.hp2 HG02165.hp2 |
synonymous_variant | LOW | c.1935C>T | p.Val645Val | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/29 | 2128/5247 | 1935/4107 | 645/1368 | chr6 | 131602378 | ||
chr6:131618485
|
C | T | 1 | a0001c0004 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.702G>A | p.Ser234Ser | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/29 | 895/5247 | 702/4107 | 234/1368 | chr6 | 131618485 | ||
chr6:131621917
|
G | A | 1 | a0001c0008 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.459C>T | p.Ser153Ser | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/29 | 652/5247 | 459/4107 | 153/1368 | chr6 | 131621917 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:131586748
|
C | T | 1 | a0001c0001t0002 | 8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*931G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 931 | chr6 | 131586748 | |||||
chr6:131586987
|
C | G | 3 | a0001c0001t0004a0001c0001t0005a0001c0001t0007 | 10 | HG02083.hp2 NA18945.hp2 NA18952.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*692G>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 692 | chr6 | 131586987 | |||||
chr6:131587149
|
T | G | 1 | a0001c0001t0004 | 5 | NA18945.hp2 NA18952.hp1 NA18959.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*530A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 530 | chr6 | 131587149 | |||||
chr6:131587411
|
T | C | 1 | a0001c0001t0006 | 2 | NA19004.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 268 | chr6 | 131587411 | |||||
chr6:131587517
|
T | G | 1 | a0001c0001t0005 | 4 | HG02083.hp2 NA18968.hp1 NA18972.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 162 | chr6 | 131587517 | |||||
chr6:131587660
|
T | C | 1 | a0001c0001t0008 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 19 | chr6 | 131587660 | |||||
chr6:131628142
|
T | C | 1 | a0001c0001t0003 | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-93A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/29 | 93 | chr6 | 131628142 | |||||
chr6:131628185
|
C | A | 1 | a0001c0001t0009 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-136G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/29 | 136 | chr6 | 131628185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:131587886
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0133 | 2 | NA18997.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3940-40C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131587886 | ||||||
chr6:131588015
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3940-169A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588015 | ||||||
chr6:131588075
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3940-229C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588075 | ||||||
chr6:131588076
|
C | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3940-230G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588076 | ||||||
chr6:131588294
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3940-448G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588294 | ||||||
chr6:131588358
|
T | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3940-512A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588358 | ||||||
chr6:131588504
|
A | T | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3940-658T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588504 | ||||||
chr6:131588691
|
A | T | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3939+774T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588691 | ||||||
chr6:131588847
|
G | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(16): Show | 24 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.3939+618C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588847 | ||||||
chr6:131588918
|
C | T | 1 | a0001c0001t0005g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3939+547G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588918 | ||||||
chr6:131589075
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3939+390C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131589075 | ||||||
chr6:131589160
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3939+305T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131589160 | ||||||
chr6:131589265
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3939+200A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131589265 | ||||||
chr6:131589632
|
C | CAA | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-38_3808-37dup others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589632 | ||||||
chr6:131589687
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3808-91G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589687 | ||||||
chr6:131589774
|
G | GA | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-179dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589774 | ||||||
chr6:131589834
|
A | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-238T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589834 | ||||||
chr6:131589853
|
C | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-257G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589853 | ||||||
chr6:131589876
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0106a0001c0001t0001g0127 | 3 | HG01952.hp1 HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.3808-280A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589876 | ||||||
chr6:131589977
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3807+345G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589977 | ||||||
chr6:131590172
|
A | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.3807+150T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131590172 | ||||||
chr6:131590515
|
A | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(113): Show | 164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.3687-73T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590515 | ||||||
chr6:131590629
|
T | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0188 | 2 | HG01123.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3687-187A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590629 | ||||||
chr6:131590652
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0089 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3687-210C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590652 | ||||||
chr6:131590714
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0109a0001c0001t0001g0141 | 4 | HG00099.hp1 HG01243.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3687-272G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590714 | ||||||
chr6:131590793
|
A | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3687-351T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590793 | ||||||
chr6:131590807
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3687-365G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590807 | ||||||
chr6:131590808
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3687-366C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590808 | ||||||
chr6:131590908
|
C | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(29): Show | 38 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.3686+405G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590908 | ||||||
chr6:131590935
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3686+378A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590935 | ||||||
chr6:131590984
|
AT | A | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(66): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3686+328delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590984 | ||||||
chr6:131590984
|
ATTT | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0207others(1): Show | 6 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3686+326_3686+328d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590984 | ||||||
chr6:131591204
|
G | A | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(7): Show | 13 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3686+109C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131591204 | ||||||
chr6:131591538
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0131 | 2 | NA18612.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.3472-11C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131591538 | ||||||
chr6:131591549
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3472-22T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131591549 | ||||||
chr6:131591897
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3472-370C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131591897 | ||||||
chr6:131592103
|
A | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.3471+285T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131592103 | ||||||
chr6:131592469
|
G | A | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-9C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131592469 | ||||||
chr6:131592953
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3398+53G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131592953 | ||||||
chr6:131592970
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3398+36T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131592970 | ||||||
chr6:131593002
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp2 | splice_region_variant&intron_variant | LOW | c.3398+4T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131593002 | ||||||
chr6:131593187
|
G | A | 1 | a0001c0001t0003g0215 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3233-16C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593187 | ||||||
chr6:131593260
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0165a0001c0001t0001g0181others(1): Show | 5 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3233-89G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593260 | ||||||
chr6:131593424
|
T | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(113): Show | 164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.3233-253A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593424 | ||||||
chr6:131593426
|
A | C | 3 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG01255.hp1 HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3233-255T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593426 | ||||||
chr6:131593462
|
TAA | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3233-293_3233-292d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593462 | ||||||
chr6:131593628
|
T | C | 4 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0052others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.3233-457A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593628 | ||||||
chr6:131593710
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3232+389G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593710 | ||||||
chr6:131593768
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3232+331T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593768 | ||||||
chr6:131593770
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3232+329A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593770 | ||||||
chr6:131593804
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3232+295A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593804 | ||||||
chr6:131593808
|
A | G | 2 | a0001c0001t0006g0176a0001c0001t0006g0183 | 2 | NA19004.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3232+291T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593808 | ||||||
chr6:131593873
|
G | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3232+226C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593873 | ||||||
chr6:131594416
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2996-81T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594416 | ||||||
chr6:131594677
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2996-342T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594677 | ||||||
chr6:131594805
|
AAAAC | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(38): Show | 75 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.2996-474_2996-471d others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594805 | ||||||
chr6:131594805
|
AAAACAAA others(1): Show |
A | 6 | a0001c0001t0001g0166a0001c0001t0003g0210a0001c0001t0003g0211others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996-478_2996-471d others(10): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594805 | ||||||
chr6:131594807
|
A | T | 1 | a0001c0001t0005g0174 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2996-472T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594807 | ||||||
chr6:131594837
|
C | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2996-502G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594837 | ||||||
chr6:131595029
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2996-694G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595029 | ||||||
chr6:131595075
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2996-740T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595075 | ||||||
chr6:131595153
|
A | G | 2 | a0001c0001t0001g0163a0001c0008t0001g0187 | 2 | NA18944.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2995+794T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595153 | ||||||
chr6:131595682
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2995+265C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595682 | ||||||
chr6:131595922
|
G | A | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2995+25C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595922 | ||||||
chr6:131596239
|
A | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(59): Show | 99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.2779-76T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596239 | ||||||
chr6:131596248
|
A | AT | 14 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(11): Show | 16 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2779-86dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596248 | ||||||
chr6:131596333
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0066a0001c0001t0001g0068 | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2779-170G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596333 | ||||||
chr6:131596502
|
C | T | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2778+16G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596502 | ||||||
chr6:131596745
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0057others(11): Show | 16 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2608-57C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596745 | ||||||
chr6:131596756
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2608-68T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596756 | ||||||
chr6:131596783
|
T | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2608-95A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596783 | ||||||
chr6:131596818
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2608-130G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596818 | ||||||
chr6:131597131
|
G | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2608-443C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597131 | ||||||
chr6:131597165
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2608-477A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597165 | ||||||
chr6:131597259
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0129a0001c0001t0001g0132 | 4 | HG02109.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2608-571C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597259 | ||||||
chr6:131597339
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0200a0001c0001t0001g0202 | 4 | NA18961.hp1 NA18997.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608-651C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597339 | ||||||
chr6:131597400
|
C | T | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2608-712G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597400 | ||||||
chr6:131597475
|
C | CA | 32 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(29): Show | 42 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.2608-788dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | ||||||
chr6:131597475
|
C | CAA | 7 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0065others(4): Show | 9 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2608-789_2608-788d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | ||||||
chr6:131597475
|
C | CAAA | 7 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209others(4): Show | 7 | HG01891.hp2 HG02258.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608-790_2608-788d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | ||||||
chr6:131597475
|
CAAAAAA | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(56): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2608-793_2608-788d others(8): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | ||||||
chr6:131597494
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0122 | 2 | HG04184.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2607+793T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597494 | ||||||
chr6:131597498
|
G | A | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2607+789C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597498 | ||||||
chr6:131597499
|
A | G | 1 | a0001c0002t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2607+788T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597499 | ||||||
chr6:131597542
|
G | GA | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2607+744dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597542 | ||||||
chr6:131597597
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0026others(17): Show | 35 | HG00609.hp1 HG01109.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.2607+690C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597597 | ||||||
chr6:131597632
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0209 | 2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2607+655A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597632 | ||||||
chr6:131597636
|
T | TC | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2607+650dupG | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597636 | ||||||
chr6:131597699
|
A | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(59): Show | 99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.2607+588T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597699 | ||||||
chr6:131597703
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0164a0001c0001t0001g0171others(4): Show | 8 | HG01433.hp2 HG01928.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2607+584C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597703 | ||||||
chr6:131597864
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2607+423A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597864 | ||||||
chr6:131598053
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2607+234G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598053 | ||||||
chr6:131598090
|
A | AAAAAACA others(11): Show |
6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2607+179_2607+196d others(20): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598090 | ||||||
chr6:131598143
|
G | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2607+144C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598143 | ||||||
chr6:131598252
|
T | G | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2607+35A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598252 | ||||||
chr6:131598519
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0165a0001c0001t0001g0181others(1): Show | 5 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2426+37A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 19/28 | chr6 | 131598519 | ||||||
chr6:131598855
|
C | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2221-94G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131598855 | ||||||
chr6:131598923
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2221-162T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131598923 | ||||||
chr6:131599077
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2221-316G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599077 | ||||||
chr6:131599106
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2221-345G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599106 | ||||||
chr6:131599263
|
A | T | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2221-502T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599263 | ||||||
chr6:131599463
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2220+575C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599463 | ||||||
chr6:131599517
|
G | C | 1 | a0001c0001t0003g0213 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2220+521C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599517 | ||||||
chr6:131599841
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2220+197G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599841 | ||||||
chr6:131599908
|
C | T | 3 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG01255.hp1 HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2220+130G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599908 | ||||||
chr6:131599984
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2220+54C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599984 | ||||||
chr6:131600180
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2096-18C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600180 | ||||||
chr6:131600333
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0198 | 5 | HG00609.hp2 HG02027.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.2096-171A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600333 | ||||||
chr6:131600426
|
C | A | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2096-264G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600426 | ||||||
chr6:131600517
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2096-355T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600517 | ||||||
chr6:131600600
|
A | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2096-438T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600600 | ||||||
chr6:131600639
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0208 | 3 | HG03041.hp1 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2096-477A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600639 | ||||||
chr6:131600749
|
A | ATT | 19 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(16): Show | 24 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.2096-588_2096-587i others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600749 | ||||||
chr6:131600755
|
T | C | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2096-593A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600755 | ||||||
chr6:131600908
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2096-746C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600908 | ||||||
chr6:131601038
|
CT | C | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(87): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2096-877delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601038 | ||||||
chr6:131601038
|
CTT | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(20): Show | 29 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.2096-878_2096-877d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601038 | ||||||
chr6:131601109
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2096-947C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601109 | ||||||
chr6:131601442
|
T | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2095+776A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601442 | ||||||
chr6:131601471
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0103others(2): Show | 5 | HG00423.hp2 HG03942.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2095+747T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601471 | ||||||
chr6:131601728
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2095+490T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601728 | ||||||
chr6:131601762
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2095+456A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601762 | ||||||
chr6:131601855
|
ACTT | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2095+360_2095+362d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601855 | ||||||
chr6:131601920
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2095+298A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601920 | ||||||
chr6:131602143
|
C | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2095+75G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131602143 | ||||||
chr6:131602414
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1932-33T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602414 | ||||||
chr6:131602631
|
T | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0129a0001c0001t0001g0132 | 4 | HG02109.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932-250A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602631 | ||||||
chr6:131602641
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1932-260C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602641 | ||||||
chr6:131602991
|
T | C | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG02257.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1931+39A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602991 | ||||||
chr6:131603270
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1757-66T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603270 | ||||||
chr6:131603421
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1757-217A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603421 | ||||||
chr6:131603469
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1757-265A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603469 | ||||||
chr6:131603495
|
TC | T | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1757-292delG | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603495 | ||||||
chr6:131603516
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1757-312T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603516 | ||||||
chr6:131603549
|
G | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(59): Show | 99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1757-345C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603549 | ||||||
chr6:131603565
|
A | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0149a0001c0001t0001g0151others(2): Show | 6 | HG02622.hp1 HG03098.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1757-361T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603565 | ||||||
chr6:131603678
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1757-474C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603678 | ||||||
chr6:131603780
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0209 | 2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1756+398A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603780 | ||||||
chr6:131603852
|
A | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1756+326T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603852 | ||||||
chr6:131603963
|
C | A | 1 | a0004c0005t0001g0078 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1756+215G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603963 | ||||||
chr6:131603987
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1756+191G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603987 | ||||||
chr6:131604518
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1614-198G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131604518 | ||||||
chr6:131604569
|
A | G | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614-249T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131604569 | ||||||
chr6:131604667
|
T | C | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG02257.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1614-347A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131604667 | ||||||
chr6:131605027
|
T | G | 1 | a0001c0001t0001g0011 | 3 | HG03831.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1613+213A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605027 | ||||||
chr6:131605040
|
A | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0026others(17): Show | 35 | HG00609.hp1 HG01109.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.1613+200T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605040 | ||||||
chr6:131605067
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1613+173G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605067 | ||||||
chr6:131605119
|
CT | C | 17 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0072others(14): Show | 19 | HG00642.hp2 HG01109.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1613+120delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605119 | ||||||
chr6:131605194
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(49): Show | 88 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1613+46G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605194 | ||||||
chr6:131605199
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1613+41G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605199 | ||||||
chr6:131605204
|
C | T | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1613+36G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605204 | ||||||
chr6:131605572
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0173a0001c0001t0006g0176others(1): Show | 5 | HG00621.hp1 HG01978.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368-87G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131605572 | ||||||
chr6:131605726
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1368-241A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131605726 | ||||||
chr6:131605867
|
C | G | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(113): Show | 164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1368-382G>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131605867 | ||||||
chr6:131606253
|
T | TA | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+225dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606253 | ||||||
chr6:131606254
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1367+225T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606254 | ||||||
chr6:131606329
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1367+150G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606329 | ||||||
chr6:131606331
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1367+148C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606331 | ||||||
chr6:131606369
|
G | C | 8 | a0001c0001t0001g0033a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 9 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367+110C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606369 | ||||||
chr6:131606431
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1367+48C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606431 | ||||||
chr6:131606724
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1222-100C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131606724 | ||||||
chr6:131606856
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1222-232A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131606856 | ||||||
chr6:131606868
|
G | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(113): Show | 164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1222-244C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131606868 | ||||||
chr6:131607468
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG00621.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1221+460G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607468 | ||||||
chr6:131607502
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02080.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1221+426C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607502 | ||||||
chr6:131607542
|
T | TAAC | 4 | a0001c0001t0001g0173a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG00621.hp1 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+383_1221+385d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607542 | ||||||
chr6:131607731
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1221+197A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607731 | ||||||
chr6:131608132
|
G | GT | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-62dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608132 | ||||||
chr6:131608169
|
A | AC | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1078-99dupG | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608169 | ||||||
chr6:131608248
|
G | A | 1 | a0001c0001t0001g0019 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1078-177C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608248 | ||||||
chr6:131608314
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-243C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608314 | ||||||
chr6:131608319
|
T | TA | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-249dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608319 | ||||||
chr6:131608384
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1078-313G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608384 | ||||||
chr6:131608475
|
A | AT | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-405dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608475 | ||||||
chr6:131608611
|
T | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(114): Show | 165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1078-540A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608611 | ||||||
chr6:131608651
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1078-580G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608651 | ||||||
chr6:131608846
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1078-775A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608846 | ||||||
chr6:131608984
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1078-913G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608984 | ||||||
chr6:131608988
|
A | G | 8 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-917T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608988 | ||||||
chr6:131609326
|
G | A | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1077+720C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609326 | ||||||
chr6:131609494
|
T | C | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1077+552A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609494 | ||||||
chr6:131609506
|
C | CT | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0142others(2): Show | 7 | HG01934.hp2 HG02165.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+539dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | ||||||
chr6:131609506
|
CT | C | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(89): Show | 136 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1077+539delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | ||||||
chr6:131609506
|
CTT | C | 13 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(10): Show | 16 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1077+538_1077+539d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | ||||||
chr6:131609506
|
CTTTTTTT others(2): Show |
C | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+531_1077+539d others(11): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | ||||||
chr6:131609555
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1077+491C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609555 | ||||||
chr6:131609572
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1077+474C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609572 | ||||||
chr6:131609616
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077+430A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609616 | ||||||
chr6:131609716
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1077+330T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609716 | ||||||
chr6:131609733
|
CATATATA others(7): Show |
C | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1077+299_1077+312d others(16): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609733 | ||||||
chr6:131609746
|
G | GTATA | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+296_1077+299d others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609746 | ||||||
chr6:131609746
|
GTA | G | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+298_1077+299d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609746 | ||||||
chr6:131609809
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1077+237G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609809 | ||||||
chr6:131609952
|
T | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(60): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1077+94A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609952 | ||||||
chr6:131610423
|
G | A | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.877-177C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131610423 | ||||||
chr6:131610862
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.877-616G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131610862 | ||||||
chr6:131611143
|
T | C | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.877-897A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611143 | ||||||
chr6:131611207
|
A | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0135 | 3 | NA18966.hp2 NA19070.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.877-961T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611207 | ||||||
chr6:131611472
|
T | C | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.877-1226A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611472 | ||||||
chr6:131611810
|
A | C | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.877-1564T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611810 | ||||||
chr6:131612221
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1975A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131612221 | ||||||
chr6:131612443
|
A | C | 5 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.877-2197T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131612443 | ||||||
chr6:131612598
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.877-2352T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131612598 | ||||||
chr6:131613076
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.877-2830A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613076 | ||||||
chr6:131613080
|
CAAGA | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(61): Show | 101 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.876+2823_876+2826d others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613080 | ||||||
chr6:131613082
|
A | G | 8 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+2825T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613082 | ||||||
chr6:131613145
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.876+2762C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613145 | ||||||
chr6:131613311
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.876+2596C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613311 | ||||||
chr6:131613592
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02300.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+2315C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613592 | ||||||
chr6:131613672
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.876+2235G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613672 | ||||||
chr6:131613823
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.876+2084A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613823 | ||||||
chr6:131613841
|
CAAT | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(50): Show | 89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.876+2063_876+2065d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613841 | ||||||
chr6:131613846
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(50): Show | 89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.876+2061C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613846 | ||||||
chr6:131613849
|
T | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(50): Show | 89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.876+2058A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613849 | ||||||
chr6:131614266
|
T | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(114): Show | 165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.876+1641A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131614266 | ||||||
chr6:131614841
|
T | C | 5 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+1066A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131614841 | ||||||
chr6:131614862
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.876+1045A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131614862 | ||||||
chr6:131615065
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.876+842G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615065 | ||||||
chr6:131615066
|
CA | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.876+840delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615066 | ||||||
chr6:131615066
|
CAA | C | 18 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 22 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.876+839_876+840del others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615066 | ||||||
chr6:131615082
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.876+825T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615082 | ||||||
chr6:131615184
|
GTTT | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(52): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.876+720_876+722del others(3): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615184 | ||||||
chr6:131615503
|
C | CA | 40 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(37): Show | 51 | HG00741.hp1 HG00741.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.876+403dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
C | CAA | 13 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0027others(10): Show | 17 | HG01123.hp2 HG01884.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.876+402_876+403dup others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
C | CAAA | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(8): Show | 21 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.876+401_876+403dup others(3): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
C | CAAAA | 29 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0014others(26): Show | 45 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.876+400_876+403dup others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
C | CAAAAA | 13 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0036others(10): Show | 17 | HG02148.hp2 HG02895.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+399_876+403dup others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
C | CAAAAAA | 7 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0161others(4): Show | 13 | HG00423.hp1 HG01192.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.876+398_876+403dup others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.876+387_876+403dup others(17): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0016 | 3 | HG02572.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.876+386_876+403dup others(18): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131615503
|
CA | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG02257.hp1 HG02258.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+403delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | ||||||
chr6:131616266
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.781-264G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616266 | ||||||
chr6:131616445
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.781-443T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616445 | ||||||
chr6:131616915
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.781-913A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616915 | ||||||
chr6:131616991
|
C | T | 3 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG01255.hp1 HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.781-989G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616991 | ||||||
chr6:131617016
|
G | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0196 | 6 | HG01934.hp1 HG02083.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1014C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617016 | ||||||
chr6:131617037
|
A | G | 8 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-1035T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617037 | ||||||
chr6:131617041
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.781-1039A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617041 | ||||||
chr6:131617165
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.781-1163A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617165 | ||||||
chr6:131617195
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-1193C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617195 | ||||||
chr6:131617331
|
C | T | 1 | a0001c0001t0003g0213 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.780+1076G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617331 | ||||||
chr6:131617369
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0195 | 3 | NA18946.hp1 NA18999.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.780+1038T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617369 | ||||||
chr6:131617398
|
C | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0066others(3): Show | 9 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.780+1009G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617398 | ||||||
chr6:131617398
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+1009G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617398 | ||||||
chr6:131617445
|
C | T | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+962G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617445 | ||||||
chr6:131617452
|
G | A | 1 | a0001c0001t0001g0011 | 3 | HG03831.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.780+955C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617452 | ||||||
chr6:131617464
|
CT | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0040others(20): Show | 29 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.780+942delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617464 | ||||||
chr6:131617647
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.780+760A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617647 | ||||||
chr6:131617920
|
T | G | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.780+487A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617920 | ||||||
chr6:131618021
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.780+386A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618021 | ||||||
chr6:131618126
|
TAATC | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+277_780+280del others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618126 | ||||||
chr6:131618215
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+192C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618215 | ||||||
chr6:131618245
|
G | A | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+162C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618245 | ||||||
chr6:131618302
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 30 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.780+105A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618302 | ||||||
chr6:131618389
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.780+18A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618389 | ||||||
chr6:131618641
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-122A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618641 | ||||||
chr6:131618834
|
C | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.668-315G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618834 | ||||||
chr6:131618911
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.668-392T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618911 | ||||||
chr6:131618925
|
A | G | 8 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.668-406T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618925 | ||||||
chr6:131619048
|
G | A | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.668-529C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619048 | ||||||
chr6:131619224
|
G | C | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.667+603C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619224 | ||||||
chr6:131619282
|
A | G | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG02257.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.667+545T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619282 | ||||||
chr6:131619283
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.667+544T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619283 | ||||||
chr6:131619344
|
T | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(114): Show | 165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.667+483A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619344 | ||||||
chr6:131619476
|
T | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.667+351A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619476 | ||||||
chr6:131619722
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.667+105T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619722 | ||||||
chr6:131619750
|
A | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(114): Show | 165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.667+77T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619750 | ||||||
chr6:131619756
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0082a0001c0001t0001g0141others(1): Show | 5 | HG00099.hp2 HG01243.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.667+71G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619756 | ||||||
chr6:131620539
|
C | G | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.597+89G>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 7/28 | chr6 | 131620539 | ||||||
chr6:131620589
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.597+39C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 7/28 | chr6 | 131620589 | ||||||
chr6:131620593
|
AT | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 7 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+34delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 7/28 | chr6 | 131620593 | ||||||
chr6:131620804
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.496-75T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620804 | ||||||
chr6:131620807
|
T | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-78A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620807 | ||||||
chr6:131620943
|
T | C | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496-214A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620943 | ||||||
chr6:131620949
|
T | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 7 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-220A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620949 | ||||||
chr6:131620953
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.496-224G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620953 | ||||||
chr6:131620983
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496-254A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620983 | ||||||
chr6:131621002
|
C | A | 1 | a0001c0004t0001g0194 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.496-273G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621002 | ||||||
chr6:131621003
|
A | G | 1 | a0001c0004t0001g0194 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.496-274T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621003 | ||||||
chr6:131621049
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.496-320C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621049 | ||||||
chr6:131621148
|
C | T | 19 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(16): Show | 24 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.496-419G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621148 | ||||||
chr6:131621224
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-495C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621224 | ||||||
chr6:131621297
|
A | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0209 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-568T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621297 | ||||||
chr6:131621370
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.495+511G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621370 | ||||||
chr6:131621391
|
A | C | 1 | a0001c0004t0001g0194 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.495+490T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621391 | ||||||
chr6:131621572
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.495+309C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621572 | ||||||
chr6:131621690
|
A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(7): Show | 14 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+191T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621690 | ||||||
chr6:131622098
|
C | CAG | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.397-121_397-120dup others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622098 | ||||||
chr6:131622328
|
C | T | 8 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.397-349G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622328 | ||||||
chr6:131622374
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.397-395T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622374 | ||||||
chr6:131622510
|
T | C | 1 | a0003c0007t0001g0139 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.397-531A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622510 | ||||||
chr6:131622557
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0066others(3): Show | 9 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.397-578A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622557 | ||||||
chr6:131622572
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397-593C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622572 | ||||||
chr6:131622643
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.397-664A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622643 | ||||||
chr6:131622647
|
A | G | 1 | a0004c0005t0001g0078 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.397-668T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622647 | ||||||
chr6:131623119
|
G | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.396+232C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131623119 | ||||||
chr6:131623177
|
C | A | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+174G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131623177 | ||||||
chr6:131623311
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.396+40A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131623311 | ||||||
chr6:131623529
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.285-67T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131623529 | ||||||
chr6:131623648
|
T | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.285-186A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131623648 | ||||||
chr6:131623934
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.285-472C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131623934 | ||||||
chr6:131624155
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.285-693A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624155 | ||||||
chr6:131624159
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.285-697T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624159 | ||||||
chr6:131624334
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+531A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624334 | ||||||
chr6:131624469
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0045 | 3 | HG01884.hp2 HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284+396G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624469 | ||||||
chr6:131624591
|
G | A | 24 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 30 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.284+274C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624591 | ||||||
chr6:131624597
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284+268C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624597 | ||||||
chr6:131624821
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(2): Show | 7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+44A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624821 | ||||||
chr6:131625352
|
G | C | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-363C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625352 | ||||||
chr6:131625385
|
G | C | 16 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 21 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.160-396C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625385 | ||||||
chr6:131625434
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0207 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-445G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625434 | ||||||
chr6:131625863
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160-874G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625863 | ||||||
chr6:131625888
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.160-899G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625888 | ||||||
chr6:131626100
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01109.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.160-1111G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626100 | ||||||
chr6:131626122
|
C | CA | 30 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 37 | HG01496.hp2 HG01884.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.160-1134dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626122 | ||||||
chr6:131626122
|
CA | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 11 | HG01257.hp1 HG01891.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-1134delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626122 | ||||||
chr6:131626137
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.160-1148T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626137 | ||||||
chr6:131626280
|
T | A | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+1116A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626280 | ||||||
chr6:131626558
|
A | C | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+838T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626558 | ||||||
chr6:131626821
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.159+575T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626821 | ||||||
chr6:131627010
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(7): Show | 14 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.159+386A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627010 | ||||||
chr6:131627045
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0045 | 3 | HG01884.hp2 HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.159+351T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627045 | ||||||
chr6:131627134
|
C | T | 6 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+262G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627134 | ||||||
chr6:131627156
|
G | GT | 7 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0206others(4): Show | 9 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+239dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627156 | ||||||
chr6:131627156
|
GT | G | 7 | a0001c0001t0001g0157a0001c0001t0003g0210a0001c0001t0003g0211others(4): Show | 7 | HG01192.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+239delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627156 | ||||||
chr6:131627167
|
T | A | 1 | a0001c0001t0001g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.159+229A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627167 | ||||||
chr6:131627182
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.159+214C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627182 | ||||||
chr6:131627317
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.159+79A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627317 | ||||||
chr6:131627329
|
GA | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(97): Show | 142 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.159+66delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627329 | ||||||
chr6:131627329
|
GAA | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 16 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.159+65_159+66delTT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627329 | ||||||
chr6:131627329
|
GAAA | G | 8 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0003g0210others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+64_159+66delTT others(1): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627329 | ||||||
chr6:131627579
|
T | C | 1 | a0001c0001t0001g0035 | 2 | HG00621.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.71+62A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 2/28 | chr6 | 131627579 | ||||||
chr6:131627676
|
T | TA | 13 | a0001c0001t0001g0028a0001c0001t0001g0147a0001c0001t0001g0148others(10): Show | 14 | HG01192.hp2 HG02622.hp1 HG02683.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.40-5dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627676 | ||||||
chr6:131627676
|
T | TAA | 51 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 78 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(75): Show |
splice_region_variant&intron_variant | LOW | c.40-6_40-5dupTT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627676 | ||||||
chr6:131627676
|
T | TAAA | 22 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 37 | HG00408.hp1 HG00423.hp1 HG02027.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.40-7_40-5dupTTT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627676 | ||||||
chr6:131627865
|
T | C | 16 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 21 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.39+146A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627865 |