Item | Value |
---|---|
geneid | 9968 |
ensemblid | ENSG00000184634.17 |
hgncid | 11957 |
symbol | MED12 |
name | mediator complex subunit 12 |
refseq_nuc | NM_005120.3 |
refseq_prot | NP_005111.2 |
ensembl_nuc | ENST00000374080.8 |
ensembl_prot | ENSP00000363193.3 |
mane_status | MANE Select |
chr | chrX |
start | 71118596 |
end | 71142450 |
strand | + |
ver | v1.2 |
region | chrX:71118596-71142450 |
region5000 | chrX:71113596-71147450 |
regionname0 | MED12_chrX_71118596_71142450 |
regionname5000 | MED12_chrX_71113596_71147450 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001 | 1/1 | 2177 | 257 | 77 | 51 | 94 | 6 | 27 | 71 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0002 | 0/0 | 2181 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0003 | 0/0 | 2177 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0004 | 0/0 | 467 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0005 | 0/0 | 2177 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0006 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0007 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0008 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0009 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0010 | 0/0 | 897 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0011 | 0/0 | 580 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0012 | 0/0 | 338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0013 | 0/0 | 83 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 6534 | 213 | 61 | 34 | 88 | 3 | 26 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0002 | 0/1 | 6534 | 16 | 0 | 10 | 1 | 3 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0003 | 0/0 | 6534 | 10 | 1 | 6 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0004 | 0/0 | 6534 | 8 | 8 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0005 | 0/0 | 6546 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0006 | 0/0 | 6534 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0007 | 0/0 | 6534 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0008 | 0/0 | 6534 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0009 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0010 | 0/0 | 6535 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0011 | 0/0 | 6533 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0012 | 0/0 | 6533 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0013 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0014 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0015 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0016 | 0/0 | 6552 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0017 | 0/0 | 6533 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0018 | 0/0 | 6535 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0019 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0020 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0021 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0022 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0023 | 0/0 | 6532 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0024 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
c0025 | 0/0 | 6536 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 392 | 273 | 80 | 53 | 104 | 6 | 28 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 9 | 1 | 3 | 0 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0002 | 1/0 | 13 | 0 | 2 | 7 | 0 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0003 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0004 | 0/0 | 12 | 1 | 5 | 2 | 1 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0005 | 0/0 | 11 | 2 | 1 | 7 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0006 | 0/0 | 10 | 2 | 6 | 0 | 1 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0007 | 0/0 | 9 | 1 | 4 | 3 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0008 | 0/0 | 6 | 1 | 1 | 2 | 0 | 2 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0010 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0017 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0032 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0017 | 0/0 | 6533 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0001 | 1/0 | 6534 | 213 | 61 | 34 | 88 | 3 | 26 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0002 | 0/1 | 6534 | 16 | 0 | 10 | 1 | 3 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0003 | 0/0 | 6534 | 10 | 1 | 6 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0004 | 0/0 | 6534 | 8 | 8 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0006 | 0/0 | 6534 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0008 | 0/0 | 6534 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0009 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0013 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0014 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0020 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0021 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0001c0024 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0002c0005 | 0/0 | 6546 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0003c0007 | 0/0 | 6534 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0004c0023 | 0/0 | 6532 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0005c0022 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0006c0019 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0007c0018 | 0/0 | 6535 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0008c0016 | 0/0 | 6552 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0009c0015 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0010c0012 | 0/0 | 6533 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0011c0011 | 0/0 | 6533 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0012c0010 | 0/0 | 6535 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 | |
a0013c0025 | 0/0 | 6536 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0017t0001 | 0/0 | 6924 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0001t0001 | 1/0 | 6925 | 213 | 61 | 34 | 88 | 3 | 26 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0002t0001 | 0/1 | 6925 | 16 | 0 | 10 | 1 | 3 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0003t0001 | 0/0 | 6925 | 10 | 1 | 6 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0004t0001 | 0/0 | 6925 | 8 | 8 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0006t0001 | 0/0 | 6925 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0008t0001 | 0/0 | 6925 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0009t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0013t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0014t0001 | 0/0 | 6925 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0020t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0021t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0001c0024t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0002c0005t0001 | 0/0 | 6937 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0003c0007t0001 | 0/0 | 6925 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0004c0023t0001 | 0/0 | 6923 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0005c0022t0001 | 0/0 | 6925 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0006c0019t0001 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0007c0018t0001 | 0/0 | 6926 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0008c0016t0001 | 0/0 | 6943 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0009c0015t0001 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0010c0012t0001 | 0/0 | 6924 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0011c0011t0001 | 0/0 | 6924 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0012c0010t0001 | 0/0 | 6926 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
a0013c0025t0001 | 0/0 | 6927 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | copy fasta | chrX | 71113596 | 71147450 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0017t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0001 | 0/0 | 15 | 8 | 1 | 3 | 0 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0002 | 1/0 | 10 | 0 | 0 | 6 | 0 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0003 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0004 | 0/0 | 8 | 0 | 2 | 2 | 1 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0005 | 0/0 | 10 | 2 | 0 | 7 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0007 | 0/0 | 9 | 1 | 4 | 3 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0008 | 0/0 | 6 | 1 | 1 | 2 | 0 | 2 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0017 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0002t0001g0006 | 0/0 | 8 | 0 | 6 | 0 | 1 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0002t0001g0032 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0003t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0003t0001g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0004t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0004t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0008t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0013t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0014t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0020t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0021t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0001c0024t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0002c0005t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0002c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0003c0007t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0003c0007t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0004c0023t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0005c0022t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0006c0019t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0007c0018t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0008c0016t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0009c0015t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0010c0012t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0011c0011t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0012c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
a0013c0025t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0010 | EUR | GBR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00738 | hp1 | a0001 | c0014 | t0001 | g0048 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01257 | hp1 | a0003 | c0007 | t0001 | g0005 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01258 | hp1 | a0003 | c0007 | t0001 | g0117 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01884 | hp2 | a0001 | c0008 | t0001 | g0035 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01975 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CDX | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02615 | hp2 | a0001 | c0013 | t0001 | g0142 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02630 | hp1 | a0001 | c0021 | t0001 | g0141 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02630 | hp2 | a0002 | c0005 | t0001 | g0006 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02818 | hp2 | a0001 | c0008 | t0001 | g0035 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0046 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02886 | hp2 | a0001 | c0020 | t0001 | g0138 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0045 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03516 | hp1 | a0001 | c0024 | t0001 | g0001 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03579 | hp1 | a0002 | c0005 | t0001 | g0006 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03669 | hp2 | a0005 | c0022 | t0001 | g0010 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18940 | hp1 | a0010 | c0012 | t0001 | g0051 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18949 | hp2 | a0000 | c0017 | t0001 | g0128 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18974 | hp1 | a0006 | c0019 | t0001 | g0087 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18979 | hp1 | a0009 | c0015 | t0001 | g0059 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18988 | hp1 | a0001 | c0006 | t0001 | g0061 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19001 | hp2 | a0008 | c0016 | t0001 | g0122 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19030 | hp2 | a0001 | c0009 | t0001 | g0049 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19056 | hp1 | a0012 | c0010 | t0001 | g0127 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19059 | hp1 | a0007 | c0018 | t0001 | g0150 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19059 | hp2 | a0004 | c0023 | t0001 | g0047 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19076 | hp1 | a0013 | c0025 | t0001 | g0036 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19086 | hp1 | a0011 | c0011 | t0001 | g0031 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19088 | hp1 | a0001 | c0006 | t0001 | g0065 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ASW | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0032 | EUR | TSI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA21309 | hp1 | a0002 | c0005 | t0001 | g0145 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0032 | REF | REF | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:71119710 | A | AT | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.231dupT | p.Ala78fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 3/45 | 391/6925 | 232/6534 | 78/2177 | INFO_REALIGN_3_PRIME | chrX | 71119710 | |
chrX:71121023 | T | TG | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.607dupG | p.Glu203fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/45 | 767/6925 | 608/6534 | 203/2177 | INFO_REALIGN_3_PRIME | chrX | 71121023 | |
chrX:71121062 | TG | T | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.647delG | p.Gly216fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/45 | 806/6925 | 647/6534 | 216/2177 | INFO_REALIGN_3_PRIME | chrX | 71121062 | |
chrX:71121123 | AC | A | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.708delC | p.Glu237fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/45 | 867/6925 | 708/6534 | 236/2177 | INFO_REALIGN_3_PRIME | chrX | 71121123 | |
chrX:71121577 | G | GT | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.864dupT | p.Gln289fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/45 | 1024/6925 | 865/6534 | 289/2177 | INFO_REALIGN_3_PRIME | chrX | 71121577 | |
chrX:71121631 | G | GC | 1 | a0012 | 1 | NA19056.hp1 | frameshift_variant | HIGH | c.919dupC | p.Leu307fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/45 | 1079/6925 | 920/6534 | 307/2177 | INFO_REALIGN_3_PRIME | chrX | 71121631 | |
chrX:71122200 | A | AC | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1104dupC | p.Ile369fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/45 | 1264/6925 | 1105/6534 | 369/2177 | INFO_REALIGN_3_PRIME | chrX | 71122200 | |
chrX:71122209 | CT | C | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1112delT | p.Leu371fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/45 | 1271/6925 | 1112/6534 | 371/2177 | chrX | 71122209 | ||
chrX:71122245 | C | CT | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1148dupT | p.Thr384fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/45 | 1308/6925 | 1149/6534 | 383/2177 | INFO_REALIGN_3_PRIME | chrX | 71122245 | |
chrX:71122250 | T | TG | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1153dupG | p.Asp385fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/45 | 1313/6925 | 1154/6534 | 385/2177 | INFO_REALIGN_3_PRIME | chrX | 71122250 | |
chrX:71122296 | GC | G | 1 | a0013 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1202delC | p.Pro401fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/45 | 1361/6925 | 1202/6534 | 401/2177 | INFO_REALIGN_3_PRIME | chrX | 71122296 | |
chrX:71122306 | AC | A | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.1210delC | p.Leu404fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/45 | 1369/6925 | 1210/6534 | 404/2177 | INFO_REALIGN_3_PRIME | chrX | 71122306 | |
chrX:71122793 | T | A | 1 | a0004 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1404T>A | p.Phe468Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/45 | 1563/6925 | 1404/6534 | 468/2177 | chrX | 71122793 | ||
chrX:71123656 | TC | T | 1 | a0011 | 1 | NA19086.hp1 | frameshift_variant | HIGH | c.1683delC | p.Ser562fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 12/45 | 1842/6925 | 1683/6534 | 561/2177 | INFO_REALIGN_3_PRIME | chrX | 71123656 | |
chrX:71123710 | TC | T | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.1737delC | p.Met580fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 12/45 | 1896/6925 | 1737/6534 | 579/2177 | INFO_REALIGN_3_PRIME | chrX | 71123710 | |
chrX:71124213 | T | A | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1799T>A | p.Phe600Tyr | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1958/6925 | 1799/6534 | 600/2177 | chrX | 71124213 | ||
chrX:71124214 | C | CAT | 1 | a0010 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.1800_1801insAT | p.Cys601fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1960/6925 | 1801/6534 | 601/2177 | chrX | 71124214 | ||
chrX:71124215 | T | A | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1801T>A | p.Cys601Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1960/6925 | 1801/6534 | 601/2177 | chrX | 71124215 | ||
chrX:71124219 | AAC | A | 1 | a0010 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.1806_1807delAC | p.Glu602fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1965/6925 | 1806/6534 | 602/2177 | chrX | 71124219 | ||
chrX:71124224 | A | T | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1810A>T | p.Ile604Phe | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1969/6925 | 1810/6534 | 604/2177 | chrX | 71124224 | ||
chrX:71125058 | C | CT | 1 | a0010 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.2138_2139insT | p.Pro714fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2298/6925 | 2139/6534 | 713/2177 | chrX | 71125058 | ||
chrX:71125060 | C | T | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2140C>T | p.Pro714Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2299/6925 | 2140/6534 | 714/2177 | chrX | 71125060 | ||
chrX:71125061 | C | A | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2141C>A | p.Pro714His | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2300/6925 | 2141/6534 | 714/2177 | chrX | 71125061 | ||
chrX:71125064 | A | T | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2144A>T | p.Lys715Met | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2303/6925 | 2144/6534 | 715/2177 | chrX | 71125064 | ||
chrX:71125067 | A | T | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2147A>T | p.Glu716Val | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2306/6925 | 2147/6534 | 716/2177 | chrX | 71125067 | ||
chrX:71125070 | A | T | 1 | a0010 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2150A>T | p.Lys717Met | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2309/6925 | 2150/6534 | 717/2177 | chrX | 71125070 | ||
chrX:71125071 | GA | G | 1 | a0010 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.2152delA | p.Ile718fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2311/6925 | 2152/6534 | 718/2177 | chrX | 71125071 | ||
chrX:71126084 | C | T | 1 | a0005 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2471C>T | p.Pro824Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 18/45 | 2630/6925 | 2471/6534 | 824/2177 | chrX | 71126084 | ||
chrX:71126347 | CG | C | 1 | a0010 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.2550delG | p.Asn851fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/45 | 2709/6925 | 2550/6534 | 850/2177 | INFO_REALIGN_3_PRIME | chrX | 71126347 | |
chrX:71126380 | CT | C | 1 | a0010 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.2583delT | p.Gly862fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/45 | 2742/6925 | 2583/6534 | 861/2177 | INFO_REALIGN_3_PRIME | chrX | 71126380 | |
chrX:71127903 | T | TC | 1 | a0010 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.2993dupC | p.Val1000fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 22/45 | 3153/6925 | 2994/6534 | 998/2177 | INFO_REALIGN_3_PRIME | chrX | 71127903 | |
chrX:71132900 | G | A | 1 | a0009 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.4471G>A | p.Gly1491Arg | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 32/45 | 4630/6925 | 4471/6534 | 1491/2177 | chrX | 71132900 | ||
chrX:71133169 | CA | C | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.4577delA | p.Lys1526fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/45 | 4736/6925 | 4577/6534 | 1526/2177 | INFO_REALIGN_3_PRIME | chrX | 71133169 | |
chrX:71133203 | G | GC | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.4609dupC | p.Leu1537fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/45 | 4769/6925 | 4610/6534 | 1537/2177 | INFO_REALIGN_3_PRIME | chrX | 71133203 | |
chrX:71134358 | T | TG | 1 | a0006 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.4625dupG | p.Met1543fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/45 | 4785/6925 | 4626/6534 | 1542/2177 | INFO_REALIGN_3_PRIME | chrX | 71134358 | |
chrX:71134764 | AT | A | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.4781delT | p.Leu1594fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/45 | 4940/6925 | 4781/6534 | 1594/2177 | INFO_REALIGN_3_PRIME | chrX | 71134764 | |
chrX:71135170 | G | T | 1 | a0004 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.4942G>T | p.Val1648Phe | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/45 | 5101/6925 | 4942/6534 | 1648/2177 | chrX | 71135170 | ||
chrX:71136330 | A | AG | 1 | a0008 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.5079dupG | p.Leu1694fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5239/6925 | 5080/6534 | 1694/2177 | INFO_REALIGN_3_PRIME | chrX | 71136330 | |
chrX:71136510 | C | T | 1 | a0004 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5255C>T | p.Pro1752Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5414/6925 | 5255/6534 | 1752/2177 | chrX | 71136510 | ||
chrX:71136512 | G | C | 1 | a0004 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5257G>C | p.Ala1753Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5416/6925 | 5257/6534 | 1753/2177 | chrX | 71136512 | ||
chrX:71136522 | T | C | 1 | a0003 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.5267T>C | p.Leu1756Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5426/6925 | 5267/6534 | 1756/2177 | chrX | 71136522 | ||
chrX:71136624 | A | AG | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.5370dupG | p.Lys1791fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5530/6925 | 5371/6534 | 1791/2177 | INFO_REALIGN_3_PRIME | chrX | 71136624 | |
chrX:71136633 | G | GC | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.5380dupC | p.Gln1794fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5540/6925 | 5381/6534 | 1794/2177 | INFO_REALIGN_3_PRIME | chrX | 71136633 | |
chrX:71136905 | C | CG | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.5429dupG | p.Tyr1812fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 38/45 | 5589/6925 | 5430/6534 | 1810/2177 | INFO_REALIGN_3_PRIME | chrX | 71136905 | |
chrX:71137269 | GC | G | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.5637delC | p.Thr1880fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/45 | 5796/6925 | 5637/6534 | 1879/2177 | INFO_REALIGN_3_PRIME | chrX | 71137269 | |
chrX:71137314 | TA | T | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.5681delA | p.Lys1894fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/45 | 5840/6925 | 5681/6534 | 1894/2177 | INFO_REALIGN_3_PRIME | chrX | 71137314 | |
chrX:71137323 | T | TG | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.5689dupG | p.Val1897fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/45 | 5849/6925 | 5690/6534 | 1897/2177 | INFO_REALIGN_3_PRIME | chrX | 71137323 | |
chrX:71137324 | G | GT | 1 | a0008 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.5690dupT | p.Tyr1898fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/45 | 5850/6925 | 5691/6534 | 1897/2177 | INFO_REALIGN_3_PRIME | chrX | 71137324 | |
chrX:71137350 | GC | G | 1 | a0004 | 1 | NA19059.hp2 | frameshift_variant | HIGH | c.5719delC | p.Gln1907fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/45 | 5878/6925 | 5719/6534 | 1907/2177 | INFO_REALIGN_3_PRIME | chrX | 71137350 | |
chrX:71137828 | C | A | 1 | a0004 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5929C>A | p.His1977Asn | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/45 | 6088/6925 | 5929/6534 | 1977/2177 | chrX | 71137828 | ||
chrX:71137829 | A | C | 1 | a0004 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5930A>C | p.His1977Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/45 | 6089/6925 | 5930/6534 | 1977/2177 | chrX | 71137829 | ||
chrX:71137906 | G | GC | 1 | a0007 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.6012dupC | p.Thr2005fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/45 | 6172/6925 | 6013/6534 | 2005/2177 | INFO_REALIGN_3_PRIME | chrX | 71137906 | |
chrX:71140651 | C | CA | 1 | a0008 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.6061_6062insA | p.Leu2021fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/45 | 6221/6925 | 6062/6534 | 2021/2177 | chrX | 71140651 | ||
chrX:71140717 | C | CG | 1 | a0008 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.6128dupG | p.Ser2044fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/45 | 6288/6925 | 6129/6534 | 2043/2177 | INFO_REALIGN_3_PRIME | chrX | 71140717 | |
chrX:71141239 | CA | C | 1 | a0000 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.6279delA | p.Gln2093fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/45 | 6438/6925 | 6279/6534 | 2093/2177 | INFO_REALIGN_3_PRIME | chrX | 71141239 | |
chrX:71141246 | A | AACAGCAG | 1 | a0008 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.6285_6291dupACAGCA others(1): Show |
p.Gln2098fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/45 | 6451/6925 | 6292/6534 | 2098/2177 | INFO_REALIGN_3_PRIME | chrX | 71141246 | |
chrX:71141277 | A | AGCAGCAC | 1 | a0008 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.6315_6316insGCAGCA others(1): Show |
p.Gln2106fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/45 | 6475/6925 | 6316/6534 | 2106/2177 | chrX | 71141277 | ||
chrX:71141278 | C | A | 1 | a0008 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.6316C>A | p.Gln2106Lys | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/45 | 6475/6925 | 6316/6534 | 2106/2177 | chrX | 71141278 | ||
chrX:71141301 | A | ACAGCAAC others(5): Show |
1 | a0002 | 3 | HG02630.hp2 HG03579.hp1 NA21309.hp1 |
disruptive_inframe_insertion | MODERATE | c.6348_6359dupCCAGCA others(6): Show |
p.His2116_Gln2119dup | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/45 | 6519/6925 | 6360/6534 | 2120/2177 | INFO_REALIGN_3_PRIME | chrX | 71141301 | |
chrX:71142188 | GC | G | 1 | a0006 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.6507delC | p.Ser2170fs | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 45/45 | 6666/6925 | 6507/6534 | 2169/2177 | INFO_REALIGN_3_PRIME | chrX | 71142188 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:71119862 | G | A | 1 | a0001c0009 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.381G>A | p.Thr127Thr | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 3/45 | 540/6925 | 381/6534 | 127/2177 | chrX | 71119862 | ||
chrX:71119865 | A | G | 1 | a0001c0024 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.384A>G | p.Gln128Gln | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 3/45 | 543/6925 | 384/6534 | 128/2177 | chrX | 71119865 | ||
chrX:71122775 | G | T | 1 | a0001c0008 | 2 | HG01884.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.1386G>T | p.Val462Val | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/45 | 1545/6925 | 1386/6534 | 462/2177 | chrX | 71122775 | ||
chrX:71123671 | T | A | 1 | a0012c0010 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.1695T>A | p.Ile565Ile | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 12/45 | 1854/6925 | 1695/6534 | 565/2177 | chrX | 71123671 | ||
chrX:71124211 | G | A | 1 | a0010c0012 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.1797G>A | p.Leu599Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1956/6925 | 1797/6534 | 599/2177 | chrX | 71124211 | ||
chrX:71125065 | G | A | 1 | a0010c0012 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.2145G>A | p.Lys715Lys | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2304/6925 | 2145/6534 | 715/2177 | chrX | 71125065 | ||
chrX:71125383 | G | A | 1 | a0001c0004 | 8 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
synonymous_variant | LOW | c.2259G>A | p.Arg753Arg | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 16/45 | 2418/6925 | 2259/6534 | 753/2177 | chrX | 71125383 | ||
chrX:71126412 | G | A | 1 | a0001c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.2613G>A | p.Gln871Gln | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/45 | 2772/6925 | 2613/6534 | 871/2177 | chrX | 71126412 | ||
chrX:71126430 | C | T | 1 | a0001c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.2631C>T | p.Phe877Phe | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/45 | 2790/6925 | 2631/6534 | 877/2177 | chrX | 71126430 | ||
chrX:71127372 | C | T | 2 | a0001c0013a0001c0021 | 2 | HG02615.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.2886C>T | p.Ser962Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 21/45 | 3045/6925 | 2886/6534 | 962/2177 | chrX | 71127372 | ||
chrX:71128600 | C | T | 1 | a0001c0020 | 1 | HG02886.hp2 | splice_region_variant&synonymous_variant | LOW | c.3357C>T | p.Val1119Val | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 24/45 | 3516/6925 | 3357/6534 | 1119/2177 | chrX | 71128600 | ||
chrX:71129687 | G | A | 2 | a0001c0009a0001c0014 | 2 | HG00738.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.3699G>A | p.Ala1233Ala | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 27/45 | 3858/6925 | 3699/6534 | 1233/2177 | chrX | 71129687 | ||
chrX:71130097 | A | C | 3 | a0001c0002a0002c0005a0005c0022 | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
synonymous_variant | LOW | c.3930A>C | p.Pro1310Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/45 | 4089/6925 | 3930/6534 | 1310/2177 | chrX | 71130097 | ||
chrX:71130109 | T | C | 1 | a0001c0006 | 2 | NA18988.hp1 NA19088.hp1 |
synonymous_variant | LOW | c.3942T>C | p.Ser1314Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/45 | 4101/6925 | 3942/6534 | 1314/2177 | chrX | 71130109 | ||
chrX:71136511 | T | G | 1 | a0004c0023 | 1 | NA19059.hp2 | synonymous_variant | LOW | c.5256T>G | p.Pro1752Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5415/6925 | 5256/6534 | 1752/2177 | chrX | 71136511 | ||
chrX:71137013 | C | T | 1 | a0001c0003 | 10 | HG00609.hp1 HG01257.hp2 HG01496.hp2 others(7): Show |
synonymous_variant | LOW | c.5535C>T | p.Asn1845Asn | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 38/45 | 5694/6925 | 5535/6534 | 1845/2177 | chrX | 71137013 | ||
chrX:71137602 | T | A | 1 | a0004c0023 | 1 | NA19059.hp2 | synonymous_variant | LOW | c.5793T>A | p.Thr1931Thr | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 40/45 | 5952/6925 | 5793/6534 | 1931/2177 | chrX | 71137602 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:71118883 | G | GC | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.99+32dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71118883 | |||||
chrX:71118948 | G | GGT | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.99+97_99+98dupTG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71118948 | |||||
chrX:71119018 | T | TG | 1 | a0001c0001t0001g0037 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.99+171dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71119018 | |||||
chrX:71119024 | G | GT | 1 | a0007c0018t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.99+173dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71119024 | |||||
chrX:71119034 | A | AT | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.99+182dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71119034 | |||||
chrX:71119109 | G | GC | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.99+257dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71119109 | |||||
chrX:71119122 | C | CG | 1 | a0001c0001t0001g0149 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.100-249dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71119122 | |||||
chrX:71119145 | G | GA | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.100-226dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71119145 | |||||
chrX:71119214 | C | A | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.100-159C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | chrX | 71119214 | ||||||
chrX:71119270 | T | TC | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.100-101dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 71119270 | |||||
chrX:71119309 | A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 6 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-64A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | chrX | 71119309 | ||||||
chrX:71119358 | G | GT | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.100-15_100-14insT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | chrX | 71119358 | ||||||
chrX:71119481 | A | AG | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | splice_region_variant&intron_variant | LOW | c.204+5dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 71119481 | |||||
chrX:71119486 | ACT | A | 1 | a0001c0001t0001g0033 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.204+12_204+13delCT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 71119486 | |||||
chrX:71119535 | G | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0038 | 3 | HG00099.hp2 HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.204+58G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 2/44 | chrX | 71119535 | ||||||
chrX:71119642 | T | TC | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.205-43dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 71119642 | |||||
chrX:71119648 | C | T | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.205-38C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 2/44 | chrX | 71119648 | ||||||
chrX:71119975 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.397-39G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 3/44 | chrX | 71119975 | ||||||
chrX:71120388 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.553+218G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120388 | ||||||
chrX:71120472 | C | G | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.553+302C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120472 | ||||||
chrX:71120536 | T | A | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.553+366T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120536 | ||||||
chrX:71120583 | A | AG | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.554-384dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120583 | |||||
chrX:71120609 | A | T | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.554-362A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120609 | ||||||
chrX:71120615 | A | AT | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.554-343dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120615 | |||||
chrX:71120615 | AT | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG03490.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.554-343delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120615 | |||||
chrX:71120615 | ATT | A | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.554-344_554-343del others(2): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120615 | |||||
chrX:71120717 | T | TC | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.554-253dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120717 | |||||
chrX:71120798 | CG | C | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.554-169delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120798 | |||||
chrX:71120823 | T | TA | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.554-148_554-147ins others(1): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120823 | ||||||
chrX:71120888 | A | G | 58 | a0000c0017t0001g0128a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 100 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.554-83A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120888 | ||||||
chrX:71120928 | A | AG | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.554-42dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120928 | |||||
chrX:71120950 | C | A | 5 | a0001c0004t0001g0012a0001c0004t0001g0020a0001c0004t0001g0044others(2): Show | 8 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.554-21C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120950 | ||||||
chrX:71120960 | C | CT | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | splice_region_variant&intron_variant | LOW | c.554-8dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120960 | |||||
chrX:71121272 | T | TACTTTAT others(7): Show |
8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.736-53_736-40dupCT others(12): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chrX | 71121272 | |||||
chrX:71121291 | C | CT | 1 | a0001c0001t0001g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.736-35dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chrX | 71121291 | |||||
chrX:71121319 | A | C | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.736-8A>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/44 | chrX | 71121319 | ||||||
chrX:71121319 | AC | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | splice_region_variant&intron_variant | LOW | c.736-5delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chrX | 71121319 | |||||
chrX:71121475 | A | AG | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.846+39dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 71121475 | |||||
chrX:71121506 | G | GT | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.847-54dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 71121506 | |||||
chrX:71121542 | T | TG | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.847-19dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 71121542 | |||||
chrX:71121843 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1101+27C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | chrX | 71121843 | ||||||
chrX:71122024 | GC | G | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1102-173delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | INFO_REALIGN_3_PRIME | chrX | 71122024 | |||||
chrX:71122064 | G | A | 47 | a0000c0017t0001g0128a0001c0001t0001g0005a0001c0001t0001g0007others(44): Show | 77 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1102-136G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | chrX | 71122064 | ||||||
chrX:71122126 | GTTGGGTC | G | 1 | a0001c0004t0001g0044 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1102-71_1102-65del others(7): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | INFO_REALIGN_3_PRIME | chrX | 71122126 | |||||
chrX:71122143 | G | GA | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1102-56dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | INFO_REALIGN_3_PRIME | chrX | 71122143 | |||||
chrX:71122179 | T | C | 9 | a0001c0001t0001g0050a0001c0001t0001g0140a0001c0004t0001g0012others(6): Show | 12 | HG00738.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1102-21T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | chrX | 71122179 | ||||||
chrX:71122386 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1248+40A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/44 | chrX | 71122386 | ||||||
chrX:71122424 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1248+78G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/44 | chrX | 71122424 | ||||||
chrX:71122687 | A | AG | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1349-50dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chrX | 71122687 | |||||
chrX:71122691 | T | A | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1349-47T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 9/44 | chrX | 71122691 | ||||||
chrX:71122706 | GT | G | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1349-30delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chrX | 71122706 | |||||
chrX:71122885 | AG | A | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1485+15delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 71122885 | |||||
chrX:71122922 | TA | T | 1 | a0013c0025t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1485+50delA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 71122922 | |||||
chrX:71122970 | A | G | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1485+96A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/44 | chrX | 71122970 | ||||||
chrX:71123015 | GC | G | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1486-77delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 71123015 | |||||
chrX:71123343 | A | G | 2 | a0001c0013t0001g0142a0001c0021t0001g0141 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1617+117A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 11/44 | chrX | 71123343 | ||||||
chrX:71123771 | A | G | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1744+51A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 12/44 | chrX | 71123771 | ||||||
chrX:71124406 | T | TG | 1 | a0001c0001t0001g0139 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1974+19dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chrX | 71124406 | |||||
chrX:71124481 | G | C | 58 | a0000c0017t0001g0128a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 100 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.1974+93G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/44 | chrX | 71124481 | ||||||
chrX:71124482 | AG | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 8 | HG01243.hp1 HG01255.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1974+100delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chrX | 71124482 | |||||
chrX:71124913 | G | T | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2056-63G>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 14/44 | chrX | 71124913 | ||||||
chrX:71124913 | GT | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0143 | 2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2056-56delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 71124913 | |||||
chrX:71125235 | A | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2226+89A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/44 | chrX | 71125235 | ||||||
chrX:71125284 | TG | T | 1 | a0010c0012t0001g0051 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2227-65delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chrX | 71125284 | |||||
chrX:71125743 | C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(15): Show | 35 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.2422+30C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | chrX | 71125743 | ||||||
chrX:71125752 | T | TC | 1 | a0010c0012t0001g0051 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2422+42dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chrX | 71125752 | |||||
chrX:71125833 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2422+120T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | chrX | 71125833 | ||||||
chrX:71125833 | T | G | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2422+120T>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | chrX | 71125833 | ||||||
chrX:71125874 | T | TG | 1 | a0010c0012t0001g0051 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2423-161dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chrX | 71125874 | |||||
chrX:71125969 | A | AC | 1 | a0010c0012t0001g0051 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2423-66dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chrX | 71125969 | |||||
chrX:71126486 | TG | T | 1 | a0007c0018t0001g0150 | 1 | NA19059.hp1 | splice_region_variant&intron_variant | LOW | c.2685+6delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/44 | INFO_REALIGN_3_PRIME | chrX | 71126486 | |||||
chrX:71126590 | A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG00423.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2685+106A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/44 | chrX | 71126590 | ||||||
chrX:71126949 | A | AC | 1 | a0010c0012t0001g0051 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2686-15dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/44 | INFO_REALIGN_3_PRIME | chrX | 71126949 | |||||
chrX:71127309 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2850-27C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 20/44 | chrX | 71127309 | ||||||
chrX:71127611 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2981+144G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 21/44 | chrX | 71127611 | ||||||
chrX:71128128 | G | GC | 1 | a0001c0001t0001g0149 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3209+8_3209+9insC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 22/44 | chrX | 71128128 | ||||||
chrX:71128467 | G | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 44 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.3354+27G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 23/44 | chrX | 71128467 | ||||||
chrX:71128494 | G | A | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.3354+54G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 23/44 | chrX | 71128494 | ||||||
chrX:71128584 | G | T | 1 | a0001c0020t0001g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3355-14G>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 23/44 | chrX | 71128584 | ||||||
chrX:71128770 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3475+52C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 24/44 | chrX | 71128770 | ||||||
chrX:71128909 | CT | C | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.3475+194delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chrX | 71128909 | |||||
chrX:71129658 | A | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 8 | HG01243.hp1 HG01255.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3692-22A>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 26/44 | chrX | 71129658 | ||||||
chrX:71129877 | C | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0001g0089 | 4 | NA18979.hp2 NA19070.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.3867+22C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 27/44 | chrX | 71129877 | ||||||
chrX:71129982 | AT | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3868-51delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 71129982 | |||||
chrX:71130250 | T | TG | 1 | a0006c0019t0001g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4047+39dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71130250 | |||||
chrX:71130437 | A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0041others(11): Show | 19 | HG00423.hp2 HG00735.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.4047+223A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | chrX | 71130437 | ||||||
chrX:71130748 | T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0114a0001c0001t0001g0115 | 4 | HG01109.hp1 HG01934.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.4047+534T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | chrX | 71130748 | ||||||
chrX:71131125 | C | CT | 48 | a0000c0017t0001g0128a0001c0001t0001g0005a0001c0001t0001g0007others(45): Show | 87 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.4048-405dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | |||||
chrX:71131125 | C | CTT | 5 | a0001c0001t0001g0034a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 7 | HG01106.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.4048-406_4048-405d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | |||||
chrX:71131125 | C | CTTT | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4048-407_4048-405d others(5): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | |||||
chrX:71131125 | C | CTTTT | 12 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0041others(9): Show | 17 | HG00423.hp2 HG01081.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.4048-408_4048-405d others(6): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | |||||
chrX:71131125 | C | CTTTTT | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4048-409_4048-405d others(7): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | |||||
chrX:71131125 | CT | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 46 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.4048-405delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | |||||
chrX:71131669 | A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | NA18949.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.4119+48A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131669 | ||||||
chrX:71131796 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4119+175G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131796 | ||||||
chrX:71131815 | TG | T | 1 | a0006c0019t0001g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4119+198delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 71131815 | |||||
chrX:71131905 | A | AAT | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4120-165_4120-164d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 71131905 | |||||
chrX:71131917 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4120-156C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131917 | ||||||
chrX:71131955 | TC | T | 1 | a0006c0019t0001g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4120-114delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 71131955 | |||||
chrX:71131988 | C | T | 85 | a0000c0017t0001g0128a0001c0001t0001g0001a0001c0001t0001g0005others(82): Show | 141 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.4120-85C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131988 | ||||||
chrX:71132233 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4253+27T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 30/44 | chrX | 71132233 | ||||||
chrX:71132293 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4254-84A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 30/44 | chrX | 71132293 | ||||||
chrX:71132327 | C | T | 1 | a0001c0003t0001g0076 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4254-50C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 30/44 | chrX | 71132327 | ||||||
chrX:71132567 | T | C | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.4415+29T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132567 | ||||||
chrX:71132594 | G | GC | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4415+59dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132594 | |||||
chrX:71132597 | CG | C | 1 | a0001c0006t0001g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4415+63delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132597 | |||||
chrX:71132666 | A | G | 8 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0032others(5): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.4415+128A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132666 | ||||||
chrX:71132752 | C | CT | 1 | a0006c0019t0001g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4416-93_4416-92ins others(1): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132752 | ||||||
chrX:71132757 | C | CTCT | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-88_4416-87ins others(3): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132757 | ||||||
chrX:71132762 | T | C | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-83T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132762 | ||||||
chrX:71132767 | C | CCTCTT | 25 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0021others(22): Show | 42 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.4416-20_4416-16dup others(5): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | C | CCTCTTCT others(3): Show |
10 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0064others(7): Show | 15 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.4416-25_4416-16dup others(10): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | C | CCTCTTCT others(8): Show |
6 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0088others(3): Show | 7 | HG00423.hp1 HG01109.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4416-30_4416-16dup others(15): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | C | CCTCTTCT others(13): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0132a0001c0001t0001g0149 | 3 | HG00423.hp2 HG00741.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4416-35_4416-16dup others(20): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | C | CCTCTTCT others(18): Show |
1 | a0001c0001t0001g0090 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4416-40_4416-16dup others(25): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | C | T | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-78C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132767 | ||||||
chrX:71132767 | CCTCTT | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(22): Show | 52 | HG00639.hp1 HG00673.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.4416-20_4416-16del others(5): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | CCTCTTCT others(3): Show |
C | 10 | a0000c0017t0001g0128a0001c0001t0001g0013a0001c0001t0001g0017others(7): Show | 15 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.4416-25_4416-16del others(10): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | CCTCTTCT others(8): Show |
C | 7 | a0001c0001t0001g0014a0001c0001t0001g0040a0001c0001t0001g0094others(4): Show | 9 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.4416-30_4416-16del others(15): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | CCTCTTCT others(13): Show |
C | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0056others(2): Show | 7 | HG02280.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.4416-35_4416-16del others(20): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | CCTCTTCT others(18): Show |
C | 16 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0079others(13): Show | 32 | HG00741.hp2 HG01884.hp2 HG02165.hp2 others(29): Show |
intron_variant | MODIFIER | c.4416-40_4416-16del others(25): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | CCTCTTCT others(23): Show |
C | 7 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0144others(4): Show | 18 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.4416-45_4416-16del others(30): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132767 | CCTCTTCT others(28): Show |
C | 1 | a0001c0002t0001g0032 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4416-50_4416-16del others(35): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | |||||
chrX:71132788 | C | CCTTCTCT others(3): Show |
1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-57_4416-56ins others(10): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132788 | ||||||
chrX:71132791 | T | TTCTCTTC others(2): Show |
1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4416-52_4416-44dup others(9): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132791 | |||||
chrX:71132795 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4416-50C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132795 | ||||||
chrX:71132799 | T | TC | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-45dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132799 | |||||
chrX:71132813 | C | CT | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-31dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132813 | |||||
chrX:71132820 | CT | C | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-23delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132820 | |||||
chrX:71132825 | CTTCT | C | 1 | a0001c0001t0001g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4416-15_4416-12del others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132825 | |||||
chrX:71132968 | TG | T | 1 | a0009c0015t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4527+15delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 71132968 | |||||
chrX:71132991 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4527+35G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 32/44 | chrX | 71132991 | ||||||
chrX:71133102 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4528-21T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 32/44 | chrX | 71133102 | ||||||
chrX:71133237 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4617+25A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133237 | ||||||
chrX:71133263 | G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0095 | 3 | HG02647.hp1 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4617+51G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133263 | ||||||
chrX:71133292 | T | TG | 1 | a0006c0019t0001g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4617+85dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133292 | |||||
chrX:71133336 | G | GT | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(11): Show | 18 | HG00733.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.4617+138dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133336 | |||||
chrX:71133336 | GT | G | 1 | a0001c0001t0001g0057 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4617+138delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133336 | |||||
chrX:71133545 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4617+333G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133545 | ||||||
chrX:71133565 | C | CT | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4617+354dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133565 | |||||
chrX:71133605 | A | AT | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4617+395dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133605 | |||||
chrX:71133605 | A | T | 2 | a0001c0003t0001g0073a0001c0003t0001g0084 | 2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.4617+393A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133605 | ||||||
chrX:71133609 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4617+397C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133609 | ||||||
chrX:71133808 | T | TG | 1 | a0001c0006t0001g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4618-547dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133808 | |||||
chrX:71133814 | G | A | 5 | a0001c0004t0001g0012a0001c0004t0001g0020a0001c0004t0001g0044others(2): Show | 8 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.4618-543G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133814 | ||||||
chrX:71133830 | G | GA | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4618-524dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133830 | |||||
chrX:71133947 | T | TG | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4618-408dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133947 | |||||
chrX:71133987 | TG | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4618-367delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133987 | |||||
chrX:71134046 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.4618-311G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71134046 | ||||||
chrX:71134052 | A | AC | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4618-301dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71134052 | |||||
chrX:71134217 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4618-140C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71134217 | ||||||
chrX:71134230 | C | CA | 26 | a0000c0017t0001g0128a0001c0001t0001g0021a0001c0001t0001g0022others(23): Show | 41 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.4618-106dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71134230 | |||||
chrX:71134230 | C | CAA | 2 | a0001c0001t0001g0135a0001c0002t0001g0144 | 2 | HG02074.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4618-107_4618-106d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71134230 | |||||
chrX:71134230 | CA | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0058others(8): Show | 14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4618-106delA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71134230 | |||||
chrX:71134252 | C | A | 2 | a0001c0002t0001g0010a0005c0022t0001g0010 | 5 | HG00099.hp1 HG00642.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.4618-105C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71134252 | ||||||
chrX:71134298 | T | TC | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4618-57dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71134298 | |||||
chrX:71134466 | A | AG | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | splice_donor_variant&intron_variant | HIGH | c.4727+1dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134466 | |||||
chrX:71134475 | TC | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4727+13delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134475 | |||||
chrX:71134565 | TGG | T | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4727+100_4727+101d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | chrX | 71134565 | ||||||
chrX:71134585 | T | C | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4727+119T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | chrX | 71134585 | ||||||
chrX:71134586 | C | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4727+120C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | chrX | 71134586 | ||||||
chrX:71134595 | G | GT | 1 | a0001c0001t0001g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4728-114dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134595 | |||||
chrX:71134608 | TG | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4728-102delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134608 | |||||
chrX:71134649 | GC | G | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4728-63delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | chrX | 71134649 | ||||||
chrX:71134657 | C | CT | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4728-51dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134657 | |||||
chrX:71134676 | TTTC | T | 3 | a0001c0001t0001g0111a0001c0013t0001g0142a0001c0021t0001g0141 | 3 | HG02615.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4728-31_4728-29del others(3): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134676 | |||||
chrX:71134687 | G | GT | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4728-22dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134687 | |||||
chrX:71134915 | CT | C | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4863+69delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/44 | INFO_REALIGN_3_PRIME | chrX | 71134915 | |||||
chrX:71134934 | AC | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4863+88delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/44 | INFO_REALIGN_3_PRIME | chrX | 71134934 | |||||
chrX:71134961 | T | G | 1 | a0001c0001t0001g0033 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4863+113T>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/44 | chrX | 71134961 | ||||||
chrX:71134966 | TA | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4863+119delA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/44 | chrX | 71134966 | ||||||
chrX:71135038 | C | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0147others(2): Show | 8 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4864-54C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/44 | chrX | 71135038 | ||||||
chrX:71135270 | GC | G | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5025+20delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135270 | |||||
chrX:71135277 | TC | T | 1 | a0007c0018t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.5025+27delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135277 | |||||
chrX:71135325 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5025+72T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135325 | ||||||
chrX:71135373 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5025+120C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135373 | ||||||
chrX:71135381 | AC | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5025+130delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135381 | |||||
chrX:71135399 | A | AG | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5025+147dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135399 | |||||
chrX:71135408 | CTT | C | 11 | a0001c0001t0001g0111a0001c0002t0001g0006a0001c0002t0001g0010others(8): Show | 23 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.5025+156_5025+157d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135408 | ||||||
chrX:71135494 | T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0088a0001c0001t0001g0089 | 4 | NA18979.hp2 NA19070.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.5025+241T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135494 | ||||||
chrX:71135522 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5025+269C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135522 | ||||||
chrX:71135538 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5025+285A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135538 | ||||||
chrX:71135580 | CT | C | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5025+331delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135580 | |||||
chrX:71135692 | AC | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5025+442delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135692 | |||||
chrX:71135815 | CT | C | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-461delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135815 | |||||
chrX:71135829 | CT | C | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-450delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135829 | |||||
chrX:71135852 | A | AC | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-428dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71135852 | |||||
chrX:71135861 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5026-420C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135861 | ||||||
chrX:71136010 | C | CCT | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-270_5026-269i others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71136010 | |||||
chrX:71136012 | C | G | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-269C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136012 | ||||||
chrX:71136014 | C | CG | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-267_5026-266i others(3): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136014 | ||||||
chrX:71136017 | G | GC | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5026-258dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71136017 | |||||
chrX:71136029 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5026-252G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136029 | ||||||
chrX:71136032 | A | T | 11 | a0001c0001t0001g0111a0001c0002t0001g0006a0001c0002t0001g0010others(8): Show | 23 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.5026-249A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136032 | ||||||
chrX:71136072 | GC | G | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-207delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71136072 | |||||
chrX:71136091 | TGCCCCAC others(34): Show |
T | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5026-189_5026-149d others(43): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136091 | ||||||
chrX:71136092 | G | C | 95 | a0000c0017t0001g0128a0001c0001t0001g0001a0001c0001t0001g0005others(92): Show | 163 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.5026-189G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136092 | ||||||
chrX:71136185 | C | CT | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-95dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71136185 | |||||
chrX:71136241 | TA | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-38delA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71136241 | |||||
chrX:71136254 | C | CT | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-25dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 71136254 | |||||
chrX:71136662 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | splice_region_variant&intron_variant | LOW | c.5400+7G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136662 | ||||||
chrX:71136742 | TA | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5400+89delA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | INFO_REALIGN_3_PRIME | chrX | 71136742 | |||||
chrX:71136748 | A | AG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5400+97dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | INFO_REALIGN_3_PRIME | chrX | 71136748 | |||||
chrX:71136748 | AG | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5400+97delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | INFO_REALIGN_3_PRIME | chrX | 71136748 | |||||
chrX:71136792 | T | C | 101 | a0000c0017t0001g0128a0001c0001t0001g0001a0001c0001t0001g0005others(98): Show | 173 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(170): Show |
intron_variant | MODIFIER | c.5401-87T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136792 | ||||||
chrX:71136833 | C | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5401-46C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136833 | ||||||
chrX:71136854 | C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 45 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.5401-25C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136854 | ||||||
chrX:71137075 | TC | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5551+51delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 71137075 | |||||
chrX:71137122 | T | TC | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5552-64dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 71137122 | |||||
chrX:71137398 | A | AG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5748+19dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/44 | INFO_REALIGN_3_PRIME | chrX | 71137398 | |||||
chrX:71137407 | AG | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5748+27delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/44 | INFO_REALIGN_3_PRIME | chrX | 71137407 | |||||
chrX:71137475 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5749-83A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/44 | chrX | 71137475 | ||||||
chrX:71137488 | T | TG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5749-67dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/44 | INFO_REALIGN_3_PRIME | chrX | 71137488 | |||||
chrX:71137492 | A | AG | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5749-65dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/44 | INFO_REALIGN_3_PRIME | chrX | 71137492 | |||||
chrX:71137549 | TC | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | splice_region_variant&intron_variant | LOW | c.5749-6delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/44 | INFO_REALIGN_3_PRIME | chrX | 71137549 | |||||
chrX:71137655 | A | AG | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5826+21dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chrX | 71137655 | |||||
chrX:71137987 | AG | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.6044+47delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71137987 | |||||
chrX:71138026 | G | GT | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+84dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138026 | |||||
chrX:71138029 | G | GGAC | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.6044+87_6044+89dup others(3): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138029 | |||||
chrX:71138080 | C | T | 1 | a0001c0006t0001g0065 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6044+137C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138080 | ||||||
chrX:71138169 | AG | A | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.6044+230delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138169 | |||||
chrX:71138233 | TC | T | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.6044+293delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138233 | |||||
chrX:71138264 | T | TC | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+322dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138264 | |||||
chrX:71138294 | T | TG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+354dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138294 | |||||
chrX:71138382 | C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0041others(10): Show | 18 | HG00423.hp2 HG00735.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.6044+439C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138382 | ||||||
chrX:71138493 | A | AT | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+556dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138493 | |||||
chrX:71138570 | C | CA | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+636dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138570 | |||||
chrX:71138579 | AT | A | 1 | a0007c0018t0001g0150 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.6044+645delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138579 | |||||
chrX:71138580 | T | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 45 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.6044+637T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138580 | ||||||
chrX:71138593 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6044+650A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138593 | ||||||
chrX:71138596 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6044+653C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138596 | ||||||
chrX:71138629 | A | AC | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+687dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138629 | |||||
chrX:71138642 | A | AG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+701dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138642 | |||||
chrX:71138660 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6044+717A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138660 | ||||||
chrX:71138836 | C | CG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+893_6044+894i others(3): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138836 | ||||||
chrX:71138886 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6044+943A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138886 | ||||||
chrX:71138903 | T | TA | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+962dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71138903 | |||||
chrX:71139045 | C | CA | 2 | a0001c0001t0001g0069a0010c0012t0001g0051 | 2 | HG02080.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.6044+1110dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139045 | |||||
chrX:71139045 | CA | C | 1 | a0004c0023t0001g0047 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.6044+1110delA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139045 | |||||
chrX:71139053 | A | AC | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+1115dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139053 | |||||
chrX:71139196 | G | GA | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+1254dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139196 | |||||
chrX:71139221 | T | TG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6044+1281dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139221 | |||||
chrX:71139313 | G | GA | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-1318dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139313 | |||||
chrX:71139449 | A | AG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-1181dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139449 | |||||
chrX:71139500 | C | CA | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-1134dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139500 | |||||
chrX:71139656 | T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG00423.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.6045-979T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71139656 | ||||||
chrX:71139821 | C | A | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-814C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71139821 | ||||||
chrX:71139948 | A | AG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-686dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71139948 | |||||
chrX:71140058 | A | AT | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-570dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140058 | |||||
chrX:71140080 | C | CT | 13 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0001g0125others(10): Show | 25 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.6045-538dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140080 | |||||
chrX:71140080 | C | CTT | 4 | a0001c0001t0001g0111a0001c0002t0001g0144a0001c0013t0001g0142others(1): Show | 4 | HG02074.hp1 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.6045-539_6045-538d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140080 | |||||
chrX:71140080 | CT | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0054others(4): Show | 11 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.6045-538delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140080 | |||||
chrX:71140144 | A | G | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0092others(3): Show | 8 | HG01123.hp2 HG01361.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.6045-491A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140144 | ||||||
chrX:71140246 | T | C | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0119others(5): Show | 11 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.6045-389T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140246 | ||||||
chrX:71140257 | A | AT | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-373dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140257 | |||||
chrX:71140274 | G | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0147a0001c0001t0001g0148 | 4 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.6045-361G>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140274 | ||||||
chrX:71140366 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.6045-269G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140366 | ||||||
chrX:71140488 | T | TC | 1 | a0006c0019t0001g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.6045-143dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140488 | |||||
chrX:71140871 | A | AT | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6267+17dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | INFO_REALIGN_3_PRIME | chrX | 71140871 | |||||
chrX:71140894 | C | A | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6267+37C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71140894 | ||||||
chrX:71140907 | A | AG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6267+52dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | INFO_REALIGN_3_PRIME | chrX | 71140907 | |||||
chrX:71141041 | T | TG | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-186dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | INFO_REALIGN_3_PRIME | chrX | 71141041 | |||||
chrX:71141114 | A | G | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-116A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71141114 | ||||||
chrX:71141116 | G | C | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-114G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71141116 | ||||||
chrX:71141117 | C | A | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-113C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71141117 | ||||||
chrX:71141136 | A | AC | 1 | a0008c0016t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-91dupC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | INFO_REALIGN_3_PRIME | chrX | 71141136 | |||||
chrX:71141162 | A | AG | 1 | a0000c0017t0001g0128 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6268-67dupG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | INFO_REALIGN_3_PRIME | chrX | 71141162 | |||||
chrX:71141423 | C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 45 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.6408+53C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141423 | ||||||
chrX:71141618 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6408+248G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141618 | ||||||
chrX:71141758 | T | C | 96 | a0000c0017t0001g0128a0001c0001t0001g0001a0001c0001t0001g0005others(93): Show | 164 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.6409-125T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141758 | ||||||
chrX:71141769 | T | C | 52 | a0000c0017t0001g0128a0001c0001t0001g0005a0001c0001t0001g0007others(49): Show | 84 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.6409-114T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141769 | ||||||
chrX:71141801 | C | CA | 21 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0085others(18): Show | 36 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.6409-71dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | INFO_REALIGN_3_PRIME | chrX | 71141801 | |||||
chrX:71141992 | AC | A | 1 | a0000c0017t0001g0128 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6490+32delC | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chrX | 71141992 | |||||
chrX:71142015 | G | C | 1 | a0000c0017t0001g0128 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6490+51G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142015 | ||||||
chrX:71142016 | C | G | 1 | a0000c0017t0001g0128 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6490+52C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142016 | ||||||
chrX:71142087 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.6491-88C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142087 | ||||||
chrX:71142117 | G | A | 14 | a0001c0001t0001g0034a0001c0001t0001g0148a0001c0002t0001g0006others(11): Show | 30 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.6491-58G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142117 |