geneid | 8712 |
---|---|
ensemblid | ENSG00000068985.5 |
hgncid | 4107 |
symbol | PAGE1 |
name | PAGE family member 1 |
refseq_nuc | NM_003785.4 |
refseq_prot | NP_003776.2 |
ensembl_nuc | ENST00000376150.4 |
ensembl_prot | ENSP00000365320.3 |
mane_status | MANE Select |
chr | chrX |
start | 49687447 |
end | 49695984 |
strand | - |
ver | v1.2 |
region | chrX:49687447-49695984 |
region5000 | chrX:49682447-49700984 |
regionname0 | PAGE1_chrX_49687447_49695984 |
regionname5000 | PAGE1_chrX_49682447_49700984 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 146 | 313 | 68 | 44 | 159 | 9 | 31 | 126 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0002 | 0/0 | 146 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0003 | 0/0 | 146 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0004 | 0/0 | 115 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0005 | 0/0 | 146 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0006 | 0/0 | 146 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 441 | 306 | 66 | 43 | 156 | 9 | 30 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
c0002 | 0/0 | 441 | 5 | 5 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
c0003 | 0/0 | 441 | 5 | 0 | 1 | 3 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
c0004 | 0/0 | 441 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
c0005 | 0/0 | 441 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
c0006 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
c0007 | 0/0 | 441 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
c0008 | 0/0 | 441 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 219 | 309 | 62 | 45 | 159 | 9 | 32 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
t0002 | 0/0 | 219 | 8 | 7 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
t0003 | 0/0 | 219 | 4 | 4 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
t0004 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0022 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 441 | 306 | 66 | 43 | 156 | 9 | 30 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0001c0003 | 0/0 | 441 | 5 | 0 | 1 | 3 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0001c0004 | 0/0 | 441 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0002c0002 | 0/0 | 441 | 5 | 5 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0003c0007 | 0/0 | 441 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0004c0006 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0005c0005 | 0/0 | 441 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0006c0008 | 0/0 | 441 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 659 | 294 | 55 | 42 | 156 | 9 | 30 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0001c0001t0002 | 0/0 | 659 | 8 | 7 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0001c0001t0003 | 0/0 | 659 | 4 | 4 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0001c0003t0001 | 0/0 | 659 | 5 | 0 | 1 | 3 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0001c0004t0001 | 0/0 | 659 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0002c0002t0001 | 0/0 | 659 | 5 | 5 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0003c0007t0001 | 0/0 | 659 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0004c0006t0004 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0005c0005t0001 | 0/0 | 659 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
a0006c0008t0001 | 0/0 | 659 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | copy fasta | chrX | 49682447 | 49700984 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0003c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0004c0006t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0005c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0006c0008t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | FIN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00639 | hp1 | a0005 | c0005 | t0001 | g0039 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01074 | hp1 | a0006 | c0008 | t0001 | g0272 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0270 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0141 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03486 | hp2 | a0004 | c0006 | t0004 | g0052 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0267 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04184 | hp1 | a0003 | c0007 | t0001 | g0108 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0268 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0269 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0271 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ASW | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0140 | AFR | USA | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0110 | REF | REF | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0185 | REF | REF | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
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:49687552
|
A | AT | 1 | a0004 | 1 | HG03486.hp2 | frameshift_variant | HIGH | c.429dupA | p.Ser144fs | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 6/6 | 553/659 | 429/441 | 143/146 | chrX | 49687552 | ||
chrX:49689423
|
T | C | 1 | a0003 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.413A>G | p.Glu138Gly | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/6 | 537/659 | 413/441 | 138/146 | chrX | 49689423 | ||
chrX:49689453
|
A | G | 1 | a0002 | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
missense_variant | MODERATE | c.383T>C | p.Leu128Pro | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/6 | 507/659 | 383/441 | 128/146 | chrX | 49689453 | ||
chrX:49689491
|
A | AC | 1 | a0004 | 1 | HG03486.hp2 | frameshift_variant | HIGH | c.344dupG | p.Cys115fs | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/6 | 468/659 | 344/441 | 115/146 | chrX | 49689491 | ||
chrX:49694716
|
A | T | 1 | a0005 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.55T>A | p.Ser19Thr | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/6 | 179/659 | 55/441 | 19/146 | chrX | 49694716 | ||
chrX:49694743
|
G | A | 1 | a0006 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.28C>T | p.Arg10Trp | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/6 | 152/659 | 28/441 | 10/146 | chrX | 49694743 |
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:49689527
|
C | T | 1 | a0001c0004 | 2 | HG02647.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.309G>A | p.Ala103Ala | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/6 | 433/659 | 309/441 | 103/146 | chrX | 49689527 | ||
chrX:49694178
|
G | A | 1 | a0001c0003 | 5 | HG01978.hp1 HG03704.hp2 NA18950.hp1 others(2): Show |
synonymous_variant | LOW | c.87C>T | p.Asp29Asp | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/6 | 211/659 | 87/441 | 29/146 | chrX | 49694178 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:49687523
|
AT | A | 1 | a0004c0006t0004 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17delA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 6/6 | 17 | chrX | 49687523 | |||||
chrX:49695897
|
G | A | 1 | a0001c0001t0003 | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/6 | chrX | 49695897 | ||||||
chrX:49695936
|
C | T | 1 | a0001c0001t0002 | 8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-76G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/6 | 1166 | chrX | 49695936 |
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:49687624
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0194 | 2 | HG01934.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.419-61T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687624 | ||||||
chrX:49687653
|
GT | G | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.419-91delA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687653 | ||||||
chrX:49687690
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.419-127C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687690 | ||||||
chrX:49687706
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-143C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687706 | ||||||
chrX:49687984
|
A | AT | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.419-422dupA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687984 | ||||||
chrX:49688031
|
CG | C | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.419-469delC | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688031 | ||||||
chrX:49688100
|
T | G | 1 | a0001c0001t0001g0008 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.419-537A>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688100 | ||||||
chrX:49688191
|
C | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0002others(5): Show | 11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-628G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688191 | ||||||
chrX:49688230
|
A | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0125a0001c0001t0001g0144others(7): Show | 11 | HG01243.hp1 HG01891.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-667T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688230 | ||||||
chrX:49688234
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.419-671T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688234 | ||||||
chrX:49688250
|
A | AC | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.419-688dupG | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688250 | ||||||
chrX:49688487
|
G | GC | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.419-925dupG | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688487 | ||||||
chrX:49688560
|
AT | A | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+857delA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688560 | ||||||
chrX:49688694
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.418+724C>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688694 | ||||||
chrX:49688721
|
G | GA | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+696dupT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688721 | ||||||
chrX:49688733
|
A | G | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+685T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688733 | ||||||
chrX:49689101
|
T | C | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0002others(5): Show | 11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.418+317A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49689101 | ||||||
chrX:49689287
|
GC | G | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+130delG | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49689287 | ||||||
chrX:49689546
|
T | TA | 14 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0109others(11): Show | 14 | HG00099.hp2 HG01952.hp1 HG02071.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.293-4dupT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
T | TAA | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 12 | HG00323.hp1 HG01069.hp1 HG01978.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.293-5_293-4dupTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
T | TAAA | 5 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0137others(2): Show | 7 | HG01070.hp2 HG02523.hp1 NA18955.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.293-6_293-4dupTTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
T | TAAAA | 10 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0096others(7): Show | 12 | HG00140.hp1 HG01258.hp1 HG01261.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.293-7_293-4dupTTTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
T | TAAAAA | 3 | a0001c0001t0001g0139a0001c0001t0001g0170a0001c0001t0001g0205 | 3 | HG03491.hp2 HG03688.hp1 NA18983.hp1 |
splice_region_variant&intron_variant | LOW | c.293-8_293-4dupTTTT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
T | TAAAAAA | 2 | a0001c0001t0001g0078a0001c0001t0001g0102 | 2 | HG02572.hp1 NA19090.hp1 |
splice_region_variant&intron_variant | LOW | c.293-9_293-4dupTTTT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
T | TAAAAAAA | 1 | a0001c0001t0001g0182 | 1 | NA18977.hp1 | splice_region_variant&intron_variant | LOW | c.293-10_293-4dupTTT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
TA | T | 10 | a0001c0001t0001g0082a0001c0001t0001g0091a0001c0001t0001g0117others(7): Show | 11 | HG01167.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.293-4delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
TAA | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0130a0001c0001t0001g0214 | 3 | HG00323.hp2 HG02818.hp1 NA18946.hp1 |
splice_region_variant&intron_variant | LOW | c.293-5_293-4delTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
TAAA | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0081others(9): Show | 15 | HG00741.hp2 HG02015.hp1 HG02280.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.293-6_293-4delTTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
TAAAA | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0144a0001c0001t0001g0241others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG02897.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.293-7_293-4delTTTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
TAAAAAAA others(1): Show |
T | 2 | a0002c0002t0001g0048a0002c0002t0001g0049 | 2 | HG02622.hp2 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.293-11_293-4delTTT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
TAAAAAAA others(3): Show |
T | 3 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0050 | 3 | HG02965.hp1 HG03041.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.293-13_293-4delTTT others(7): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689546
|
TAAAAAAA others(13): Show |
T | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.293-23_293-4delTTT others(17): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | ||||||
chrX:49689565
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.293-34_293-23delAT others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689565 | ||||||
chrX:49689565
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0003g0031 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.293-44_293-23delAT others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689565 | ||||||
chrX:49689566
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0038 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.293-38_293-24delAT others(13): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689566 | ||||||
chrX:49689566
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0003g0032 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.293-46_293-24delAT others(21): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689566 | ||||||
chrX:49689567
|
A | T | 1 | a0002c0002t0001g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.293-24T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689567 | ||||||
chrX:49689568
|
AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.293-50_293-26delAT others(23): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689568 | ||||||
chrX:49689569
|
A | AAT | 1 | a0001c0001t0001g0155 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.293-27_293-26insAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689569 | ||||||
chrX:49689569
|
A | AATAT | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.293-27_293-26insAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689569 | ||||||
chrX:49689569
|
A | T | 4 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(1): Show | 4 | HG02622.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-26T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689569 | ||||||
chrX:49689569
|
AAAAAAAA others(1): Show |
A | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-34_293-27delAT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689569 | ||||||
chrX:49689569
|
AAAAAAAA others(17): Show |
A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.293-50_293-27delAT others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689569 | ||||||
chrX:49689570
|
AAAAAAAT others(16): Show |
A | 1 | a0001c0001t0001g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-50_293-28delAT others(21): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689570 | ||||||
chrX:49689571
|
A | AAT | 3 | a0001c0001t0001g0012a0001c0001t0001g0230a0001c0004t0001g0140 | 4 | HG00673.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-29_293-28insAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689571 | ||||||
chrX:49689571
|
A | ATAT | 1 | a0001c0001t0001g0079 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.293-29_293-28insAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689571 | ||||||
chrX:49689571
|
A | T | 8 | a0001c0001t0001g0080a0001c0001t0001g0154a0001c0001t0001g0155others(5): Show | 8 | HG02622.hp2 HG02886.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-28T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689571 | ||||||
chrX:49689571
|
AAAAAATA others(15): Show |
A | 1 | a0001c0001t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.293-50_293-29delAT others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689571 | ||||||
chrX:49689572
|
AAAAAT | A | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.293-34_293-30delAT others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689572 | ||||||
chrX:49689572
|
AAAAATAT | A | 1 | a0001c0001t0001g0132 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.293-36_293-30delAT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689572 | ||||||
chrX:49689572
|
AAAAATAT others(12): Show |
A | 1 | a0001c0001t0001g0212 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.293-48_293-30delAT others(17): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689572 | ||||||
chrX:49689572
|
AAAAATAT others(16): Show |
A | 1 | a0001c0001t0001g0008 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.293-52_293-30delAT others(21): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689572 | ||||||
chrX:49689573
|
A | AAT | 4 | a0001c0001t0001g0095a0001c0001t0001g0114a0001c0001t0001g0161others(1): Show | 4 | HG01358.hp1 HG03490.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-31_293-30insAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
A | AATAT | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.293-31_293-30insAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
A | AATATAT | 2 | a0001c0001t0001g0196a0001c0003t0001g0268 | 2 | HG01168.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.293-31_293-30insAT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.293-31_293-30insAT others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
A | AT | 3 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0202 | 3 | HG00423.hp2 HG03834.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.293-31_293-30insA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
A | ATAT | 2 | a0001c0001t0001g0250a0001c0001t0001g0266 | 2 | HG00544.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.293-31_293-30insAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
A | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0079a0001c0001t0001g0080others(15): Show | 19 | HG00099.hp1 HG00673.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.293-30T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
AAAAT | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0255 | 2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.293-34_293-31delAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
AAAATAT | A | 1 | a0001c0001t0001g0021 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.293-36_293-31delAT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
AAAATATA others(15): Show |
A | 1 | a0001c0001t0001g0178 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.293-52_293-31delAT others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689573
|
AAAATATA others(17): Show |
A | 2 | a0001c0001t0001g0229a0001c0001t0001g0248 | 2 | HG00280.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.293-54_293-31delAT others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | ||||||
chrX:49689574
|
AAAT | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0121a0001c0001t0001g0148others(2): Show | 7 | HG00558.hp2 HG01255.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-34_293-32delAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689574 | ||||||
chrX:49689574
|
AAATAT | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0263 | 2 | NA18947.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.293-36_293-32delAT others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689574 | ||||||
chrX:49689575
|
A | AAAAAAAT | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAAAAT others(2): Show |
1 | a0001c0001t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(7): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAAAT | 3 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0183 | 4 | HG02074.hp1 HG03225.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAAATA others(1): Show |
1 | a0001c0001t0001g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAAT | 4 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0187others(1): Show | 8 | HG02523.hp2 NA18941.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAATAT | 1 | a0001c0001t0001g0124 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAATAT others(2): Show |
2 | a0001c0001t0001g0197a0001c0001t0001g0213 | 2 | HG00597.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.293-33_293-32insAT others(7): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0001g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(9): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAAT | 13 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0129others(10): Show | 15 | HG00558.hp1 HG00609.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAATAT | 4 | a0001c0001t0001g0112a0001c0001t0001g0128a0001c0001t0001g0143others(1): Show | 4 | HG01123.hp1 HG01192.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAATATA others(5): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0066 | 2 | NA19055.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.293-33_293-32insAT others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0063 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.293-33_293-32insAT others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAAT | 14 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0074others(11): Show | 16 | HG00735.hp1 HG01168.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAATAT | 3 | a0001c0001t0001g0116a0001c0001t0001g0142a0001c0001t0001g0262 | 3 | HG04204.hp1 NA18952.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.293-33_293-32insAT others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAATATAT | 1 | a0001c0001t0001g0135 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAATATAT others(2): Show |
1 | a0001c0001t0001g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(7): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AAT | 7 | a0001c0001t0001g0060a0001c0001t0001g0073a0001c0001t0001g0162others(4): Show | 7 | HG00597.hp2 HG02738.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-34_293-33dupAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AATAT | 9 | a0001c0001t0001g0100a0001c0001t0001g0111a0001c0001t0001g0115others(6): Show | 9 | HG00438.hp1 HG00544.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-36_293-33dupAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AATATAT | 3 | a0001c0001t0001g0041a0001c0001t0001g0156a0001c0001t0001g0260 | 3 | HG02080.hp2 NA18967.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.293-38_293-33dupAT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AATATATA others(1): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0179 | 2 | HG02135.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.293-40_293-33dupAT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0224 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.293-42_293-33dupAT others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.293-44_293-33dupAT others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | AT | 4 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0093others(1): Show | 4 | HG02027.hp1 HG02615.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-33_293-32insA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | ATATAT | 2 | a0001c0001t0001g0068a0001c0004t0001g0141 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-33_293-32insAT others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | ATATATAT | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | ATATATAT others(2): Show |
2 | a0001c0001t0001g0072a0001c0003t0001g0271 | 2 | HG02735.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.293-33_293-32insAT others(7): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
A | T | 51 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0051others(48): Show | 54 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.293-32T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
AAT | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0067others(3): Show | 8 | HG01884.hp2 HG03669.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-34_293-33delAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
AATAT | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0094a0001c0001t0001g0099others(1): Show | 5 | HG00733.hp1 HG01106.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-36_293-33delAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689575
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0001g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.293-52_293-33delAT others(18): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | ||||||
chrX:49689576
|
AT | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0098a0001c0001t0001g0177others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-34delA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689576 | ||||||
chrX:49689576
|
ATAT | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0200a0001c0001t0002g0034others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-36_293-34delAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689576 | ||||||
chrX:49689576
|
ATATAT | A | 2 | a0001c0001t0001g0247a0001c0001t0002g0035 | 2 | HG03453.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.293-38_293-34delAT others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689576 | ||||||
chrX:49689576
|
ATATATAT | A | 1 | a0001c0001t0001g0004 | 3 | HG00642.hp1 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.293-40_293-34delAT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689576 | ||||||
chrX:49689577
|
T | A | 26 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 31 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.293-34A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689577 | ||||||
chrX:49689579
|
T | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0030others(14): Show | 20 | HG01109.hp1 HG01261.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-36A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689579 | ||||||
chrX:49689581
|
T | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0123a0001c0001t0001g0134others(2): Show | 5 | HG00639.hp1 HG01952.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-38A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689581 | ||||||
chrX:49689583
|
T | A | 2 | a0001c0001t0002g0035a0004c0006t0004g0052 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-40A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689583 | ||||||
chrX:49689593
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-50A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689593 | ||||||
chrX:49689595
|
TA | T | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-53delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689595 | ||||||
chrX:49689597
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293-54A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689597 | ||||||
chrX:49689599
|
T | C | 2 | a0001c0001t0001g0051a0002c0002t0001g0047 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.293-56A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689599 | ||||||
chrX:49689599
|
TA | T | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-57delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689599 | ||||||
chrX:49689601
|
T | C | 6 | a0001c0001t0001g0051a0002c0002t0001g0046a0002c0002t0001g0048others(3): Show | 6 | HG02622.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-58A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689601 | ||||||
chrX:49689601
|
T | TACATATA others(1): Show |
1 | a0001c0001t0001g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.293-59_293-58insGT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689601 | ||||||
chrX:49689603
|
T | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0053a0002c0002t0001g0046others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-60A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689603 | ||||||
chrX:49689605
|
T | C | 5 | a0001c0001t0001g0053a0002c0002t0001g0048a0002c0002t0001g0049others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-62A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689605 | ||||||
chrX:49689607
|
T | C | 9 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0249others(6): Show | 12 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-64A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689607 | ||||||
chrX:49689609
|
T | C | 9 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0007others(6): Show | 12 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-66A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689609 | ||||||
chrX:49689611
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 24 | HG00735.hp1 HG01993.hp2 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-68A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689611 | ||||||
chrX:49689613
|
C | T | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-70G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689613 | ||||||
chrX:49689615
|
TATAC | T | 1 | a0001c0001t0001g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293-76_293-73delGT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689615 | ||||||
chrX:49689619
|
C | CAT | 2 | a0001c0001t0001g0053a0004c0006t0004g0052 | 2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-78_293-77dupAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689619 | ||||||
chrX:49689619
|
C | T | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-76G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689619 | ||||||
chrX:49689619
|
CAT | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0139a0001c0001t0001g0182 | 3 | NA18977.hp1 NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.293-78_293-77delAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689619 | ||||||
chrX:49689629
|
T | TAC | 5 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(2): Show | 8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-88_293-87dupGT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689629 | ||||||
chrX:49689631
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-88G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689631 | ||||||
chrX:49689635
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 19 | HG00423.hp1 HG01993.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-92A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689635 | ||||||
chrX:49689642
|
ATATGTGT others(3): Show |
A | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-109_293-100del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689642 | ||||||
chrX:49689646
|
G | A | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-103C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689646 | ||||||
chrX:49689648
|
G | A | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-105C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689648 | ||||||
chrX:49689649
|
T | TATAC | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-107_293-106ins others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689649 | ||||||
chrX:49689650
|
G | A | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-107C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689650 | ||||||
chrX:49689650
|
GTGTA | G | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-111_293-108del others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689650 | ||||||
chrX:49689652
|
G | A | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-109C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689652 | ||||||
chrX:49689652
|
GTA | G | 11 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0001g0071others(8): Show | 11 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-111_293-110del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689652 | ||||||
chrX:49689653
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-110A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689653 | ||||||
chrX:49689654
|
A | G | 23 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0042others(20): Show | 24 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-111T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689654 | ||||||
chrX:49689655
|
T | C | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-112A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689655 | ||||||
chrX:49689663
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-120A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689663 | ||||||
chrX:49689663
|
T | TAC | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-121_293-120ins others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689663 | ||||||
chrX:49689665
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0053 | 3 | HG00738.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.293-122A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689665 | ||||||
chrX:49689667
|
C | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0053others(5): Show | 11 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-124G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689667 | ||||||
chrX:49689669
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(2): Show | 8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-126A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689669 | ||||||
chrX:49689671
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0053 | 3 | HG00738.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.293-128A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689671 | ||||||
chrX:49689673
|
C | CAT | 10 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0055others(7): Show | 13 | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-132_293-131dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689673 | ||||||
chrX:49689673
|
C | CATATATG others(19): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01168.hp1 HG01192.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-156_293-131dup others(26): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689673 | ||||||
chrX:49689673
|
C | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0053others(5): Show | 11 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-130G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689673 | ||||||
chrX:49689678
|
A | ATG | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-137_293-136dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689678 | ||||||
chrX:49689678
|
ATGTGTG | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-141_293-136del others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689678 | ||||||
chrX:49689686
|
A | G | 4 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-143T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689686 | ||||||
chrX:49689691
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-148A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689691 | ||||||
chrX:49689695
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-152G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689695 | ||||||
chrX:49689703
|
T | C | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-160A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689703 | ||||||
chrX:49689704
|
ATGTG | A | 1 | a0002c0002t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.293-165_293-162del others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689704 | ||||||
chrX:49689706
|
G | A | 4 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-163C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689706 | ||||||
chrX:49689706
|
GTGTATAT others(1): Show |
G | 31 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0038others(28): Show | 35 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.293-171_293-164del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689706 | ||||||
chrX:49689708
|
G | A | 4 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-165C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689708 | ||||||
chrX:49689710
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-167T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689710 | ||||||
chrX:49689712
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 22 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.293-169T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689712 | ||||||
chrX:49689714
|
A | G | 4 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-171T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689714 | ||||||
chrX:49689716
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-173C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689716 | ||||||
chrX:49689718
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(5): Show | 11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-175T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689718 | ||||||
chrX:49689722
|
A | ATACACAC others(35): Show |
1 | a0001c0001t0001g0218 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293-180_293-179ins others(42): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689722 | ||||||
chrX:49689723
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-180A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689723 | ||||||
chrX:49689723
|
T | TG | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-181dupC | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689723 | ||||||
chrX:49689724
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-181C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689724 | ||||||
chrX:49689729
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-186A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689729 | ||||||
chrX:49689733
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-190G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689733 | ||||||
chrX:49689735
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-192G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689735 | ||||||
chrX:49689737
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(9): Show | 29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-194G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689737 | ||||||
chrX:49689738
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-195T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689738 | ||||||
chrX:49689740
|
A | ATATATG | 1 | a0001c0001t0001g0218 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293-198_293-197ins others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689740 | ||||||
chrX:49689740
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-197T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689740 | ||||||
chrX:49689742
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-199T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689742 | ||||||
chrX:49689744
|
G | A | 4 | a0001c0001t0001g0218a0001c0001t0002g0002a0001c0001t0002g0007others(1): Show | 7 | HG00741.hp1 HG01081.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-201C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689744 | ||||||
chrX:49689744
|
G | GTA | 14 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0053others(11): Show | 17 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-203_293-202dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689744 | ||||||
chrX:49689744
|
GTA | G | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-203_293-202del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689744 | ||||||
chrX:49689746
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-203T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689746 | ||||||
chrX:49689748
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(5): Show | 11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-205T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689748 | ||||||
chrX:49689749
|
T | TAC | 1 | a0001c0001t0001g0038 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.293-207_293-206ins others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689749 | ||||||
chrX:49689750
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-207C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689750 | ||||||
chrX:49689752
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(4): Show | 24 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-209C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689752 | ||||||
chrX:49689755
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-212A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689755 | ||||||
chrX:49689763
|
T | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(5): Show | 11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-220A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689763 | ||||||
chrX:49689765
|
T | C | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-222A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689765 | ||||||
chrX:49689768
|
ATG | A | 1 | a0001c0001t0001g0266 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.293-227_293-226del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689768 | ||||||
chrX:49689770
|
G | A | 8 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(5): Show | 11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-227C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689770 | ||||||
chrX:49689776
|
A | ATATATAC others(25): Show |
1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.293-265_293-234dup others(32): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689776 | ||||||
chrX:49689776
|
A | ATATATGT others(7): Show |
3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-234_293-233ins others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689776 | ||||||
chrX:49689776
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02055.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-233T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689776 | ||||||
chrX:49689780
|
ATACACAC others(9): Show |
A | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-253_293-238del others(16): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689780 | ||||||
chrX:49689783
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(4): Show | 24 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-240G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689783 | ||||||
chrX:49689788
|
A | C | 1 | a0001c0001t0001g0213 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.293-245T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689788 | ||||||
chrX:49689789
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 23 | HG01081.hp1 HG01993.hp2 HG02723.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-246A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689789 | ||||||
chrX:49689794
|
A | ATG | 5 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0034others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-253_293-252dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689794 | ||||||
chrX:49689796
|
GTA | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-255_293-254del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689796 | ||||||
chrX:49689798
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-255T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689798 | ||||||
chrX:49689804
|
A | ATG | 1 | a0001c0001t0001g0004 | 3 | HG00642.hp1 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.293-263_293-262dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689804 | ||||||
chrX:49689804
|
A | ATGTGTAT others(25): Show |
1 | a0001c0001t0001g0239 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.293-293_293-262dup others(32): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689804 | ||||||
chrX:49689804
|
ATGTGTAT others(51): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-319_293-262del others(58): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689804 | ||||||
chrX:49689808
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(5): Show | 22 | HG01993.hp2 HG02622.hp2 HG02965.hp1 others(19): Show |
intron_variant | MODIFIER | c.293-265C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689808 | ||||||
chrX:49689812
|
ATACACAC others(124): Show |
A | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-400_293-270del | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689812 | ||||||
chrX:49689813
|
T | TAC | 3 | a0001c0001t0001g0088a0001c0001t0001g0124a0001c0001t0001g0134 | 3 | HG00408.hp1 HG01952.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.293-272_293-271dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689813 | ||||||
chrX:49689815
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-272G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689815 | ||||||
chrX:49689819
|
C | CACAT | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-277_293-276ins others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689819 | ||||||
chrX:49689819
|
C | CAT | 8 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0057others(5): Show | 9 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-278_293-277dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689819 | ||||||
chrX:49689819
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-276G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689819 | ||||||
chrX:49689820
|
ATATATGT others(1): Show |
A | 6 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 8 | HG00738.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-285_293-278del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689820 | ||||||
chrX:49689824
|
ATG | A | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-283_293-282del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689824 | ||||||
chrX:49689824
|
ATGTGTAT others(5): Show |
A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-293_293-282del others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689824 | ||||||
chrX:49689826
|
GTGTATAT others(1): Show |
G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-291_293-284del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689826 | ||||||
chrX:49689830
|
A | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0053a0004c0006t0004g0052 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-287T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689830 | ||||||
chrX:49689836
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0034others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-293C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689836 | ||||||
chrX:49689836
|
G | GTGTGTAT others(3): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 5 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-303_293-294dup others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689836 | ||||||
chrX:49689838
|
GTGTATAT others(7): Show |
G | 6 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 8 | HG00738.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-309_293-296del others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689838 | ||||||
chrX:49689847
|
C | T | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-304G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689847 | ||||||
chrX:49689851
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-309_293-308ins others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689851 | ||||||
chrX:49689851
|
C | T | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-308G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689851 | ||||||
chrX:49689857
|
TAG | T | 1 | a0001c0001t0001g0208 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.293-316_293-315del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689857 | ||||||
chrX:49689858
|
A | G | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-315T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689858 | ||||||
chrX:49689858
|
AGG | A | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-317_293-316del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689858 | ||||||
chrX:49689859
|
G | T | 18 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0053others(15): Show | 23 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-316C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689859 | ||||||
chrX:49689863
|
TGTATATA others(15): Show |
T | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-342_293-321del others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689863 | ||||||
chrX:49689864
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0053others(12): Show | 19 | HG00558.hp1 HG01081.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.293-321C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689864 | ||||||
chrX:49689870
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.293-327T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689870 | ||||||
chrX:49689874
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-331C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689874 | ||||||
chrX:49689885
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293-343_293-342ins others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689885 | ||||||
chrX:49689885
|
C | CATATATG others(3): Show |
1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-343_293-342ins others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689885 | ||||||
chrX:49689890
|
ATAGG | A | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-351_293-348del others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689890 | ||||||
chrX:49689892
|
AGGTGTAT others(28): Show |
A | 1 | a0001c0001t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.293-384_293-350del others(35): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689892 | ||||||
chrX:49689893
|
G | T | 13 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0002others(10): Show | 16 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-350C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689893 | ||||||
chrX:49689896
|
GTA | G | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.293-355_293-354del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689896 | ||||||
chrX:49689898
|
A | G | 10 | a0001c0001t0001g0026a0001c0001t0001g0091a0001c0001t0001g0176others(7): Show | 11 | HG00558.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-355T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689898 | ||||||
chrX:49689904
|
A | ATG | 7 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0058others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-363_293-362dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | ||||||
chrX:49689904
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0106 | 2 | HG02132.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.293-361T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | ||||||
chrX:49689904
|
ATGTGTAT others(30): Show |
A | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 36 | HG00323.hp1 HG00544.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-398_293-362del others(37): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | ||||||
chrX:49689904
|
ATGTGTAT others(66): Show |
A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.293-434_293-362del others(73): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | ||||||
chrX:49689915
|
C | T | 2 | a0001c0001t0001g0043a0004c0006t0004g0052 | 2 | HG02132.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-372G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689915 | ||||||
chrX:49689916
|
A | ATGTGTAT others(6): Show |
1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-374_293-373ins others(13): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689916 | ||||||
chrX:49689919
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-376G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689919 | ||||||
chrX:49689925
|
TAGG | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0051a0004c0006t0004g0052 | 3 | HG02132.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-385_293-383del others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689925 | ||||||
chrX:49689926
|
AG | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.293-384delC | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689926 | ||||||
chrX:49689926
|
AGGG | A | 5 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-386_293-384del others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689926 | ||||||
chrX:49689926
|
AGGGTGTA others(8): Show |
A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-398_293-384del others(15): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689926 | ||||||
chrX:49689927
|
G | GGTGTATA others(28): Show |
1 | a0001c0001t0001g0249 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.293-385_293-384ins others(35): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689927 | ||||||
chrX:49689927
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0195 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.293-384C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689927 | ||||||
chrX:49689927
|
GGGTGTAT others(30): Show |
G | 5 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0149others(2): Show | 6 | HG00558.hp2 HG03017.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-421_293-385del others(37): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689927 | ||||||
chrX:49689928
|
G | GTGTATAT others(28): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0195 | 2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.293-386_293-385ins others(35): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689928 | ||||||
chrX:49689928
|
G | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(109): Show | 131 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.293-385C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689928 | ||||||
chrX:49689933
|
A | G | 6 | a0001c0001t0001g0043a0002c0002t0001g0046a0002c0002t0001g0047others(3): Show | 6 | HG02132.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-390T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689933 | ||||||
chrX:49689939
|
ATG | A | 1 | a0001c0001t0001g0208 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.293-398_293-397del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689939 | ||||||
chrX:49689941
|
G | A | 6 | a0001c0001t0001g0043a0002c0002t0001g0046a0002c0002t0001g0047others(3): Show | 6 | HG02132.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-398C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689941 | ||||||
chrX:49689941
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0001g0051a0004c0006t0004g0052 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-399_293-398ins others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689941 | ||||||
chrX:49689944
|
TGTATATA others(5): Show |
T | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-413_293-402del others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689944 | ||||||
chrX:49689945
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-402C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689945 | ||||||
chrX:49689945
|
GTATATAC others(19): Show |
G | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.293-428_293-403del others(26): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689945 | ||||||
chrX:49689950
|
TACAC | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-411_293-408del others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689950 | ||||||
chrX:49689952
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-409G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689952 | ||||||
chrX:49689954
|
C | CA | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-412dupT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689954 | ||||||
chrX:49689956
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-413G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689956 | ||||||
chrX:49689956
|
CAT | C | 1 | a0001c0001t0001g0027 | 2 | NA18951.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.293-415_293-414del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689956 | ||||||
chrX:49689957
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-414T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689957 | ||||||
chrX:49689958
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-415A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689958 | ||||||
chrX:49689959
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-416T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689959 | ||||||
chrX:49689964
|
T | G | 13 | a0001c0001t0001g0057a0001c0001t0001g0093a0001c0001t0001g0154others(10): Show | 13 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.293-421A>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689964 | ||||||
chrX:49689965
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-422C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689965 | ||||||
chrX:49689965
|
GTGTA | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-426_293-423del others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689965 | ||||||
chrX:49689966
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-423A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689966 | ||||||
chrX:49689967
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-424C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689967 | ||||||
chrX:49689968
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-425A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689968 | ||||||
chrX:49689970
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-427A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689970 | ||||||
chrX:49689972
|
T | TACACAC | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-430_293-429ins others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689972 | ||||||
chrX:49689975
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.293-432T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689975 | ||||||
chrX:49689975
|
ATG | A | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-434_293-433del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689975 | ||||||
chrX:49689977
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0007others(1): Show | 7 | HG01081.hp1 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-434C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689977 | ||||||
chrX:49689977
|
G | GTGTATAT others(23): Show |
2 | a0001c0001t0001g0051a0004c0006t0004g0052 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-435_293-434ins others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689977 | ||||||
chrX:49689977
|
GTGTGTAT others(23): Show |
G | 1 | a0001c0001t0001g0182 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.293-464_293-435del others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689977 | ||||||
chrX:49689986
|
TAC | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-445_293-444del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689986 | ||||||
chrX:49689990
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-447G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689990 | ||||||
chrX:49690005
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-462T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690005 | ||||||
chrX:49690007
|
A | ATATGTG | 7 | a0001c0001t0001g0078a0001c0001t0001g0107a0001c0001t0001g0172others(4): Show | 7 | HG00597.hp1 HG00733.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-465_293-464ins others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690007 | ||||||
chrX:49690011
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.293-468T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690011 | ||||||
chrX:49690013
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(7): Show | 24 | HG00597.hp1 HG00733.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-470C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690013 | ||||||
chrX:49690013
|
GTGTGTAT others(35): Show |
G | 5 | a0001c0001t0001g0055a0001c0001t0001g0215a0001c0001t0001g0216others(2): Show | 5 | HG02109.hp1 NA18943.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-512_293-471del others(42): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690013 | ||||||
chrX:49690015
|
GTGTATAT others(81): Show |
G | 4 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0049others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-560_293-473del others(88): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690015 | ||||||
chrX:49690015
|
GTGTATAT others(103): Show |
G | 1 | a0002c0002t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293-582_293-473del | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690015 | ||||||
chrX:49690016
|
TGTATATA others(89): Show |
T | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-569_293-474del others(96): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690016 | ||||||
chrX:49690024
|
C | T | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-481G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690024 | ||||||
chrX:49690028
|
CAT | C | 1 | a0001c0001t0001g0078 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.293-487_293-486del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690028 | ||||||
chrX:49690029
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.293-496_293-487del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690029 | ||||||
chrX:49690039
|
G | GTA | 1 | a0006c0008t0001g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.293-498_293-497dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690039 | ||||||
chrX:49690041
|
ATATATGT others(1): Show |
A | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-506_293-499del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690041 | ||||||
chrX:49690043
|
ATATGTG | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0053others(12): Show | 19 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-506_293-501del others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690043 | ||||||
chrX:49690045
|
A | ATG | 2 | a0001c0001t0001g0106a0001c0001t0001g0164 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.293-504_293-503dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690045 | ||||||
chrX:49690047
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.293-504C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690047 | ||||||
chrX:49690049
|
G | GTGTGTAT others(23): Show |
1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.293-507_293-506ins others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690049 | ||||||
chrX:49690055
|
A | G | 16 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0053others(13): Show | 20 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-512T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690055 | ||||||
chrX:49690056
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.293-513A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690056 | ||||||
chrX:49690056
|
TGTGTATA others(3): Show |
T | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-523_293-514del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690056 | ||||||
chrX:49690066
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0027others(68): Show | 81 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.293-523G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690066 | ||||||
chrX:49690070
|
CAT | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0151a0001c0001t0001g0152 | 3 | HG00140.hp1 HG01515.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.293-529_293-528del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690070 | ||||||
chrX:49690071
|
ATATATAT others(3): Show |
A | 4 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 5 | HG01891.hp2 HG02602.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-538_293-529del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690071 | ||||||
chrX:49690071
|
ATATATAT others(13): Show |
A | 59 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0027others(56): Show | 66 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.293-548_293-529del others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690071 | ||||||
chrX:49690081
|
G | GTATATAC others(3): Show |
1 | a0001c0001t0001g0176 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.293-539_293-538ins others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690081 | ||||||
chrX:49690081
|
GTATATAT others(47): Show |
G | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293-592_293-539del others(54): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690081 | ||||||
chrX:49690082
|
TATATATG others(23): Show |
T | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-569_293-540del others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690082 | ||||||
chrX:49690083
|
ATATATGT others(1): Show |
A | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-548_293-541del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690083 | ||||||
chrX:49690088
|
T | TAC | 6 | a0001c0001t0001g0177a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG00733.hp2 HG03669.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-546_293-545ins others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690088 | ||||||
chrX:49690088
|
T | TACACATA others(39): Show |
1 | a0001c0001t0001g0178 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.293-546_293-545ins others(46): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690088 | ||||||
chrX:49690089
|
G | A | 7 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0249others(4): Show | 7 | HG00423.hp1 HG00733.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-546C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690089 | ||||||
chrX:49690090
|
T | C | 7 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0249others(4): Show | 7 | HG00423.hp1 HG00733.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-547A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690090 | ||||||
chrX:49690091
|
G | A | 7 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0249others(4): Show | 7 | HG00423.hp1 HG00733.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-548C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | ||||||
chrX:49690091
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0206 | 2 | HG01258.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.293-549_293-548ins others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | ||||||
chrX:49690091
|
G | GTATATAT others(15): Show |
29 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(26): Show | 35 | HG01884.hp1 HG01891.hp1 HG01928.hp1 others(32): Show |
intron_variant | MODIFIER | c.293-570_293-549dup others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | ||||||
chrX:49690091
|
G | GTATATAT others(37): Show |
1 | a0001c0001t0001g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.293-592_293-549dup others(44): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | ||||||
chrX:49690091
|
GTATATAT others(15): Show |
G | 16 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0054others(13): Show | 19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-570_293-549del others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | ||||||
chrX:49690092
|
TATATATG others(13): Show |
T | 3 | a0001c0001t0001g0051a0001c0001t0001g0053a0004c0006t0004g0052 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-569_293-550del others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690092 | ||||||
chrX:49690098
|
T | TAC | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-556_293-555ins others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690098 | ||||||
chrX:49690099
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-556C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690099 | ||||||
chrX:49690100
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-557A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690100 | ||||||
chrX:49690101
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-558C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690101 | ||||||
chrX:49690102
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045 | 17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-569_293-560del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690102 | ||||||
chrX:49690108
|
T | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02109.hp2 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-565A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690108 | ||||||
chrX:49690109
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-566T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690109 | ||||||
chrX:49690110
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-567G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690110 | ||||||
chrX:49690111
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-568T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690111 | ||||||
chrX:49690112
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-569G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690112 | ||||||
chrX:49690113
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0186 | 2 | HG03471.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.293-580_293-571dup others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690113 | ||||||
chrX:49690113
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.293-571_293-570ins others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690113 | ||||||
chrX:49690123
|
GTA | G | 4 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0049others(1): Show | 4 | HG02965.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-582_293-581del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690123 | ||||||
chrX:49690123
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.293-592_293-581del others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690123 | ||||||
chrX:49690135
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG02257.hp1 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.293-592T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690135 | ||||||
chrX:49690143
|
G | T | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-600C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690143 | ||||||
chrX:49690316
|
G | GT | 1 | a0004c0006t0004g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-774dupA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690316 | ||||||
chrX:49690565
|
AT | A | 1 | a0001c0001t0001g0234 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.292+683delA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690565 | ||||||
chrX:49690671
|
A | G | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0002others(5): Show | 11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.292+578T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690671 | ||||||
chrX:49690709
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.292+540A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690709 | ||||||
chrX:49690854
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.292+395C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690854 | ||||||
chrX:49690869
|
C | CA | 4 | a0001c0001t0001g0065a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG00621.hp1 HG02293.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+379dupT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690869 | ||||||
chrX:49690869
|
CA | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(13): Show | 30 | HG01934.hp1 HG01993.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.292+379delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690869 | ||||||
chrX:49691730
|
C | CA | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.167-357dupT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691730 | ||||||
chrX:49691750
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.167-376A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691750 | ||||||
chrX:49691811
|
G | A | 1 | a0006c0008t0001g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.167-437C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691811 | ||||||
chrX:49691849
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.167-475A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691849 | ||||||
chrX:49691862
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.167-488G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691862 | ||||||
chrX:49692009
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.167-635G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692009 | ||||||
chrX:49692123
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0053a0004c0006t0004g0052 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.167-749C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692123 | ||||||
chrX:49692146
|
GA | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(13): Show | 33 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.167-773delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692146 | ||||||
chrX:49692214
|
G | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(14): Show | 34 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.167-840C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692214 | ||||||
chrX:49692403
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.167-1029C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692403 | ||||||
chrX:49692456
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(14): Show | 34 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.167-1082G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692456 | ||||||
chrX:49692568
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.167-1194A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692568 | ||||||
chrX:49692622
|
C | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 14 | HG00621.hp1 HG02293.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.167-1248G>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692622 | ||||||
chrX:49692627
|
G | GT | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.167-1254dupA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692627 | ||||||
chrX:49692627
|
G | GTT | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.167-1255_167-1254d others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692627 | ||||||
chrX:49692744
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.166+1355T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692744 | ||||||
chrX:49692753
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.166+1346T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692753 | ||||||
chrX:49692783
|
A | ATTATTTA others(1): Show |
12 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0002others(9): Show | 15 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.166+1308_166+1315d others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692783 | ||||||
chrX:49692783
|
A | ATTATTTA others(5): Show |
1 | a0002c0002t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.166+1304_166+1315d others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692783 | ||||||
chrX:49692783
|
A | ATTATTTA others(9): Show |
4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.166+1300_166+1315d others(18): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692783 | ||||||
chrX:49692869
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.166+1230G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692869 | ||||||
chrX:49692901
|
T | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.166+1198A>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692901 | ||||||
chrX:49693005
|
A | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(2): Show | 8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.166+1094T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693005 | ||||||
chrX:49693041
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.166+1058A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693041 | ||||||
chrX:49693078
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033others(2): Show | 8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.166+1021A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693078 | ||||||
chrX:49693316
|
G | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0002others(5): Show | 11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.166+783C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693316 | ||||||
chrX:49693474
|
C | CT | 2 | a0001c0001t0001g0096a0001c0001t0001g0187 | 2 | HG01934.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.166+624dupA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693474 | ||||||
chrX:49693555
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.166+544A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693555 | ||||||
chrX:49693558
|
A | AT | 1 | a0001c0001t0001g0259 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.166+540dupA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693558 | ||||||
chrX:49693637
|
G | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(14): Show | 34 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.166+462C>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693637 | ||||||
chrX:49693785
|
C | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.166+314G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693785 | ||||||
chrX:49693787
|
C | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0053a0004c0006t0004g0052 | 3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.166+312G>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693787 | ||||||
chrX:49693830
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.166+269A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693830 | ||||||
chrX:49693918
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.166+181T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693918 | ||||||
chrX:49693960
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.166+139A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693960 | ||||||
chrX:49693995
|
T | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0002g0002others(5): Show | 11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.166+104A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693995 | ||||||
chrX:49694021
|
G | GAC | 27 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0037others(24): Show | 29 | HG00099.hp2 HG00408.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.166+76_166+77dupGT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694021
|
G | GACAC | 31 | a0001c0001t0001g0027a0001c0001t0001g0207a0001c0001t0001g0208others(28): Show | 32 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.166+74_166+77dupGT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694021
|
G | GACACAC | 22 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(19): Show | 27 | HG00438.hp2 HG00597.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.166+72_166+77dupGT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694021
|
G | GACACACA others(1): Show |
3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG00544.hp1 NA19005.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.166+70_166+77dupGT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694021
|
GAC | G | 20 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0043others(17): Show | 35 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.166+76_166+77delGT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694021
|
GACAC | G | 20 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(17): Show | 20 | HG00323.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.166+74_166+77delGT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694021
|
GACACAC | G | 9 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0067others(6): Show | 12 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.166+72_166+77delGT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694021
|
GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0051a0001c0001t0003g0031a0001c0001t0003g0032 | 5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+70_166+77delGT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | ||||||
chrX:49694062
|
ACAC | A | 1 | a0001c0001t0001g0257 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.166+34_166+36delGT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694062 | ||||||
chrX:49694064
|
A | ACACACC | 1 | a0001c0001t0001g0066 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.166+34_166+35insGG others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694064 | ||||||
chrX:49694064
|
A | ACC | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG00621.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.166+33_166+34dupGG | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694064 | ||||||
chrX:49694064
|
A | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063 | 3 | HG02040.hp1 NA18939.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.166+35T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694064 | ||||||
chrX:49694065
|
C | CA | 1 | a0001c0001t0001g0258 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166+33_166+34insT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694065 | ||||||
chrX:49694065
|
C | CACA | 4 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 4 | HG00544.hp2 HG02080.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.166+33_166+34insTG others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694065 | ||||||
chrX:49694065
|
C | CACACACA | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG04204.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.166+33_166+34insTG others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694065 | ||||||
chrX:49694066
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG00408.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.166+33G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694066 | ||||||
chrX:49694067
|
C | A | 1 | a0001c0001t0001g0266 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.166+32G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694067 | ||||||
chrX:49694261
|
T | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG02109.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64-60A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694261 | ||||||
chrX:49694391
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.64-190G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694391 | ||||||
chrX:49694521
|
GA | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0033 | 6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+186delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694521 | ||||||
chrX:49694555
|
C | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+153G>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694555 | ||||||
chrX:49694563
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0038others(24): Show | 47 | HG00738.hp1 HG01081.hp1 HG01993.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+145T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694563 | ||||||
chrX:49694574
|
A | AT | 9 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+133dupA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694574 | ||||||
chrX:49694591
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18956.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.63+117C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694591 | ||||||
chrX:49694593
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+115T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694593 | ||||||
chrX:49695052
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8-274G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/5 | chrX | 49695052 | ||||||
chrX:49695149
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8-371G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/5 | chrX | 49695149 | ||||||
chrX:49695680
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-9+189T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/5 | chrX | 49695680 |