geneid | 11238 |
---|---|
ensemblid | ENSG00000169239.14 |
hgncid | 1378 |
symbol | CA5B |
name | carbonic anhydrase 5B |
refseq_nuc | NM_007220.4 |
refseq_prot | NP_009151.1 |
ensembl_nuc | ENST00000318636.8 |
ensembl_prot | ENSP00000314099.3 |
mane_status | MANE Select |
chr | chrX |
start | 15738270 |
end | 15788411 |
strand | + |
ver | v1.2 |
region | chrX:15738270-15788411 |
region5000 | chrX:15733270-15793411 |
regionname0 | CA5B_chrX_15738270_15788411 |
regionname5000 | CA5B_chrX_15733270_15793411 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 317 | 271 | 67 | 43 | 119 | 11 | 29 | 94 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0002 | 0/0 | 317 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0003 | 0/0 | 317 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0004 | 0/0 | 317 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 954 | 171 | 51 | 27 | 62 | 7 | 22 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
c0002 | 0/0 | 954 | 99 | 16 | 16 | 56 | 4 | 7 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
c0003 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
c0004 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
c0005 | 0/0 | 954 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
c0006 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 5884 | 99 | 21 | 12 | 50 | 3 | 12 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0002 | 0/0 | 5883 | 79 | 9 | 12 | 48 | 3 | 7 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0003 | 0/0 | 5886 | 25 | 0 | 12 | 7 | 3 | 3 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0004 | 0/0 | 5884 | 11 | 2 | 3 | 6 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0005 | 0/0 | 5885 | 6 | 0 | 0 | 4 | 0 | 2 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0006 | 0/0 | 5883 | 6 | 6 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0007 | 0/0 | 5883 | 6 | 5 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0008 | 0/0 | 5886 | 6 | 6 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0009 | 0/0 | 5884 | 4 | 4 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0010 | 0/0 | 5881 | 3 | 3 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0011 | 0/0 | 5884 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0012 | 0/0 | 5881 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0013 | 0/0 | 5881 | 2 | 2 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0014 | 0/0 | 5886 | 2 | 0 | 1 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0015 | 0/0 | 5879 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0016 | 0/0 | 5879 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0017 | 0/0 | 5885 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0018 | 0/0 | 5885 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0019 | 0/0 | 5885 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0020 | 0/0 | 5884 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0021 | 1/0 | 5884 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0022 | 0/0 | 5884 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0023 | 0/0 | 5884 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0024 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0025 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0026 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0027 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0028 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0029 | 0/0 | 5881 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0030 | 0/0 | 5881 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0031 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0032 | 0/0 | 5886 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0033 | 0/0 | 5886 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0034 | 0/0 | 5887 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
t0035 | 0/0 | 5887 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 954 | 171 | 51 | 27 | 62 | 7 | 22 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002 | 0/0 | 954 | 99 | 16 | 16 | 56 | 4 | 7 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0004 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0002c0006 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0003c0005 | 0/0 | 954 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0004c0003 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6837 | 97 | 21 | 12 | 48 | 3 | 12 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0003 | 0/0 | 6839 | 25 | 0 | 12 | 7 | 3 | 3 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0005 | 0/0 | 6838 | 6 | 0 | 0 | 4 | 0 | 2 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0006 | 0/0 | 6836 | 6 | 6 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0008 | 0/0 | 6839 | 6 | 6 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0009 | 0/0 | 6837 | 4 | 4 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0010 | 0/0 | 6834 | 3 | 3 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0011 | 0/0 | 6837 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0012 | 0/0 | 6834 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0013 | 0/0 | 6834 | 2 | 2 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0014 | 0/0 | 6839 | 2 | 0 | 1 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0015 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0016 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0017 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0018 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0019 | 0/0 | 6838 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0020 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0021 | 1/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0022 | 0/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0023 | 0/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0029 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0030 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0031 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0032 | 0/0 | 6839 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0033 | 0/0 | 6839 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0034 | 0/0 | 6840 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0001t0035 | 0/0 | 6840 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0002 | 0/0 | 6836 | 78 | 9 | 12 | 48 | 3 | 6 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0004 | 0/0 | 6837 | 11 | 2 | 3 | 6 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0007 | 0/0 | 6836 | 5 | 4 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0024 | 0/0 | 6835 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0025 | 0/0 | 6836 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0026 | 0/0 | 6836 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0027 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0002t0028 | 0/0 | 6836 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0001c0004t0001 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0002c0006t0001 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0003c0005t0002 | 0/0 | 6836 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
a0004c0003t0007 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | copy fasta | chrX | 15733270 | 15793411 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0010g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0011g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0012g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0013g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0014g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0016g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0017g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0018g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0019g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0020g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0021g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0022g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0023g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0029g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0030g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0031g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0032g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0033g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0034g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0001t0035g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0007g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0024g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0025g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0026g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0027g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0002t0028g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0002c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0003c0005t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
a0004c0003t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0244 | EUR | GBR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00280 | hp1 | a0001 | c0002 | t0028 | g0180 | EUR | FIN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | FIN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0186 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00621 | hp1 | a0001 | c0002 | t0004 | g0205 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0176 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0245 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01071 | hp2 | a0001 | c0001 | t0012 | g0263 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0117 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0247 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01243 | hp1 | a0001 | c0002 | t0007 | g0224 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0225 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01261 | hp1 | a0001 | c0002 | t0004 | g0240 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0256 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0246 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01496 | hp1 | a0001 | c0001 | t0014 | g0248 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0200 | EUR | IBS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0040 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0227 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01891 | hp2 | a0001 | c0001 | t0031 | g0187 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0177 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CDX | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02293 | hp1 | a0001 | c0001 | t0011 | g0139 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0009 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02451 | hp1 | a0001 | c0001 | t0030 | g0257 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02451 | hp2 | a0004 | c0003 | t0007 | g0237 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02572 | hp1 | a0001 | c0002 | t0007 | g0165 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02630 | hp1 | a0001 | c0001 | t0032 | g0063 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0192 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02698 | hp1 | a0001 | c0001 | t0019 | g0151 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02717 | hp1 | a0001 | c0001 | t0016 | g0022 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02723 | hp1 | a0001 | c0001 | t0029 | g0055 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0070 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02965 | hp1 | a0001 | c0001 | t0013 | g0249 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02976 | hp2 | a0001 | c0001 | t0015 | g0023 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03492 | hp1 | a0001 | c0002 | t0026 | g0172 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03516 | hp2 | a0001 | c0001 | t0035 | g0259 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0126 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0230 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0262 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03669 | hp1 | a0003 | c0005 | t0002 | g0189 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0171 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03704 | hp1 | a0001 | c0001 | t0022 | g0107 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0175 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0085 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0197 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG04184 | hp1 | a0001 | c0001 | t0034 | g0030 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0068 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG04228 | hp1 | a0001 | c0001 | t0023 | g0109 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18522 | hp1 | a0001 | c0002 | t0007 | g0206 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | CHB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | CHB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0185 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18980 | hp2 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18981 | hp2 | a0001 | c0002 | t0004 | g0232 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18986 | hp1 | a0001 | c0001 | t0017 | g0129 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19001 | hp1 | a0001 | c0001 | t0020 | g0097 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19005 | hp1 | a0001 | c0002 | t0004 | g0201 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19007 | hp1 | a0001 | c0002 | t0004 | g0202 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19009 | hp1 | a0002 | c0006 | t0001 | g0119 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0203 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19058 | hp1 | a0001 | c0002 | t0025 | g0191 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19067 | hp1 | a0001 | c0001 | t0018 | g0081 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19075 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19076 | hp1 | a0001 | c0004 | t0001 | g0090 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19081 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19086 | hp1 | a0001 | c0002 | t0024 | g0196 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA20752 | hp1 | a0001 | c0001 | t0033 | g0004 | EUR | TSI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0013 | EUR | TSI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA20905 | hp1 | a0001 | c0001 | t0014 | g0050 | SAS | GIH | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02109 | hp1 | a0001 | c0002 | t0007 | g0231 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02109 | hp2 | a0001 | c0002 | t0004 | g0218 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG02486 | hp1 | a0001 | c0002 | t0007 | g0235 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA20300 | hp1 | a0001 | c0001 | t0013 | g0258 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0056 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
NA21309 | hp2 | a0001 | c0002 | t0027 | g0219 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0020 | REF | REF | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0021 | g0164 | REF | REF | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
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:15774323
|
G | A | 1 | a0004 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.481G>A | p.Ala161Thr | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/8 | 617/6837 | 481/954 | 161/317 | chrX | 15774323 | ||
chrX:15782588
|
G | T | 1 | a0002 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.878G>T | p.Arg293Leu | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1014/6837 | 878/954 | 293/317 | chrX | 15782588 | ||
chrX:15782623
|
C | A | 1 | a0003 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.913C>A | p.Gln305Lys | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1049/6837 | 913/954 | 305/317 | chrX | 15782623 |
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:15775293
|
G | A | 1 | a0001c0004 | 1 | NA19076.hp1 | synonymous_variant | LOW | c.603G>A | p.Pro201Pro | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/8 | 739/6837 | 603/954 | 201/317 | chrX | 15775293 | ||
chrX:15782628
|
G | A | 3 | a0001c0002a0003c0005a0004c0003 | 101 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
synonymous_variant | LOW | c.918G>A | p.Ala306Ala | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1054/6837 | 918/954 | 306/317 | chrX | 15782628 |
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:15782671
|
C | A | 2 | a0001c0001t0015a0001c0001t0016 | 2 | HG02717.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 7 | chrX | 15782671 | |||||
chrX:15782880
|
CT | C | 2 | a0001c0001t0015a0001c0001t0016 | 2 | HG02717.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*226delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 226 | INFO_REALIGN_3_PRIME | chrX | 15782880 | ||||
chrX:15783159
|
A | G | 2 | a0001c0001t0008a0001c0001t0035 | 7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*495A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 495 | chrX | 15783159 | |||||
chrX:15783207
|
A | C | 4 | a0001c0001t0003a0001c0001t0014a0001c0001t0033others(1): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*543A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 543 | chrX | 15783207 | |||||
chrX:15783520
|
A | G | 25 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(22): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*856A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 856 | chrX | 15783520 | |||||
chrX:15783623
|
C | T | 2 | a0001c0001t0008a0001c0001t0035 | 7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*959C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 959 | chrX | 15783623 | |||||
chrX:15783794
|
T | TA | 11 | a0001c0001t0010a0001c0002t0002a0001c0002t0004others(8): Show | 104 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1143dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1144 | INFO_REALIGN_3_PRIME | chrX | 15783794 | ||||
chrX:15783794
|
TA | T | 1 | a0001c0001t0006 | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1143delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1143 | INFO_REALIGN_3_PRIME | chrX | 15783794 | ||||
chrX:15783803
|
A | G | 2 | a0001c0001t0015a0001c0001t0016 | 2 | HG02717.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1139 | chrX | 15783803 | |||||
chrX:15783833
|
G | A | 18 | a0001c0001t0010a0001c0001t0012a0001c0001t0013others(15): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1169G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1169 | chrX | 15783833 | |||||
chrX:15783887
|
C | CT | 11 | a0001c0001t0005a0001c0001t0034a0001c0001t0035others(8): Show | 97 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1241dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1242 | INFO_REALIGN_3_PRIME | chrX | 15783887 | ||||
chrX:15783887
|
C | CTT | 2 | a0001c0001t0031a0001c0002t0004 | 12 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1240_*1241dupTT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1242 | INFO_REALIGN_3_PRIME | chrX | 15783887 | ||||
chrX:15783894
|
T | TC | 1 | a0001c0001t0017 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1230_*1231insC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1231 | chrX | 15783894 | |||||
chrX:15784078
|
G | A | 18 | a0001c0001t0010a0001c0001t0012a0001c0001t0013others(15): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1414G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1414 | chrX | 15784078 | |||||
chrX:15784084
|
C | T | 1 | a0001c0002t0028 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1420C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1420 | chrX | 15784084 | |||||
chrX:15784177
|
C | T | 1 | a0001c0002t0027 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1513C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1513 | chrX | 15784177 | |||||
chrX:15784677
|
C | G | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0014others(4): Show | 37 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2013C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2013 | chrX | 15784677 | |||||
chrX:15784861
|
C | T | 10 | a0001c0002t0002a0001c0002t0004a0001c0002t0007others(7): Show | 101 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2197C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2197 | chrX | 15784861 | |||||
chrX:15785049
|
A | G | 1 | a0001c0001t0030 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2385A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2385 | chrX | 15785049 | |||||
chrX:15785123
|
C | T | 1 | a0001c0002t0026 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2459 | chrX | 15785123 | |||||
chrX:15785181
|
C | G | 2 | a0001c0001t0015a0001c0001t0016 | 2 | HG02717.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2517C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2517 | chrX | 15785181 | |||||
chrX:15785291
|
A | G | 1 | a0001c0001t0023 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2627A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2627 | chrX | 15785291 | |||||
chrX:15785448
|
A | G | 1 | a0001c0001t0011 | 2 | HG02293.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2784A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2784 | chrX | 15785448 | |||||
chrX:15785513
|
G | A | 18 | a0001c0001t0010a0001c0001t0012a0001c0001t0013others(15): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2849G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2849 | chrX | 15785513 | |||||
chrX:15785514
|
T | C | 1 | a0001c0001t0029 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2850T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2850 | chrX | 15785514 | |||||
chrX:15785864
|
A | AT | 6 | a0001c0001t0003a0001c0001t0008a0001c0001t0032others(3): Show | 35 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3209dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3210 | INFO_REALIGN_3_PRIME | chrX | 15785864 | ||||
chrX:15785867
|
T | TA | 15 | a0001c0001t0012a0001c0001t0013a0001c0001t0029others(12): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3203_*3204insA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3204 | chrX | 15785867 | |||||
chrX:15785868
|
T | TA | 1 | a0001c0001t0014 | 2 | HG01496.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3204_*3205insA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3205 | chrX | 15785868 | |||||
chrX:15785902
|
G | A | 3 | a0001c0001t0010a0001c0001t0015a0001c0001t0016 | 5 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3238G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3238 | chrX | 15785902 | |||||
chrX:15785983
|
G | A | 1 | a0001c0001t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3319G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3319 | chrX | 15785983 | |||||
chrX:15786091
|
G | T | 1 | a0001c0001t0022 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3427G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3427 | chrX | 15786091 | |||||
chrX:15786263
|
T | TA | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0014others(4): Show | 37 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3600dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3601 | INFO_REALIGN_3_PRIME | chrX | 15786263 | ||||
chrX:15786385
|
C | A | 1 | a0001c0001t0010 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3721C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3721 | chrX | 15786385 | |||||
chrX:15786399
|
T | C | 1 | a0001c0001t0012 | 2 | HG01071.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3735T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3735 | chrX | 15786399 | |||||
chrX:15786648
|
ACTTC | A | 18 | a0001c0001t0010a0001c0001t0012a0001c0001t0013others(15): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3991_*3994delTCCT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3991 | INFO_REALIGN_3_PRIME | chrX | 15786648 | ||||
chrX:15786860
|
C | T | 3 | a0001c0002t0007a0001c0002t0027a0004c0003t0007 | 7 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4196C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4196 | chrX | 15786860 | |||||
chrX:15786861
|
G | A | 5 | a0001c0001t0003a0001c0001t0014a0001c0001t0032others(2): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4197G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4197 | chrX | 15786861 | |||||
chrX:15786863
|
C | T | 1 | a0001c0001t0012 | 2 | HG01071.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4199C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4199 | chrX | 15786863 | |||||
chrX:15786895
|
G | A | 1 | a0001c0001t0033 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4231G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4231 | chrX | 15786895 | |||||
chrX:15787448
|
G | A | 38 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(35): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*4784G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4784 | chrX | 15787448 | |||||
chrX:15787658
|
T | TA | 1 | a0001c0001t0018 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5000dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5001 | INFO_REALIGN_3_PRIME | chrX | 15787658 | ||||
chrX:15787668
|
A | G | 5 | a0001c0001t0003a0001c0001t0014a0001c0001t0032others(2): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5004A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5004 | chrX | 15787668 | |||||
chrX:15787723
|
G | A | 1 | a0001c0001t0012 | 2 | HG01071.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5059G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5059 | chrX | 15787723 | |||||
chrX:15787735
|
G | T | 25 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(22): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*5071G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5071 | chrX | 15787735 | |||||
chrX:15787903
|
G | C | 1 | a0001c0001t0009 | 4 | HG01884.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5239G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5239 | chrX | 15787903 | |||||
chrX:15787979
|
A | T | 1 | a0001c0001t0029 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5315A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5315 | chrX | 15787979 | |||||
chrX:15788004
|
G | T | 3 | a0001c0001t0010a0001c0001t0015a0001c0001t0016 | 5 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5340G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5340 | chrX | 15788004 | |||||
chrX:15788104
|
G | C | 2 | a0001c0001t0008a0001c0001t0035 | 7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5440G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5440 | chrX | 15788104 | |||||
chrX:15788123
|
C | T | 1 | a0001c0001t0020 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5459C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5459 | chrX | 15788123 | |||||
chrX:15788159
|
G | T | 2 | a0001c0001t0013a0001c0001t0030 | 3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5495G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5495 | chrX | 15788159 | |||||
chrX:15788217
|
A | AT | 1 | a0001c0001t0019 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5554dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5555 | INFO_REALIGN_3_PRIME | chrX | 15788217 | ||||
chrX:15788286
|
A | T | 1 | a0001c0002t0025 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5622A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5622 | chrX | 15788286 |
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:15738368
|
C | T | 2 | a0001c0001t0012g0262a0001c0001t0012g0263 | 2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+16C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738368 | ||||||
chrX:15738377
|
T | TG | 1 | a0001c0001t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-54+31dupG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15738377 | |||||
chrX:15738704
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(10): Show | 15 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.-54+352T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738704 | ||||||
chrX:15738755
|
C | A | 3 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013 | 3 | HG01346.hp1 HG01433.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-54+403C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738755 | ||||||
chrX:15738759
|
G | A | 6 | a0001c0001t0008g0024a0001c0001t0010g0025a0001c0001t0010g0026others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+407G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738759 | ||||||
chrX:15738771
|
A | C | 1 | a0001c0001t0003g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-54+419A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738771 | ||||||
chrX:15738985
|
C | T | 2 | a0001c0001t0013g0258a0001c0001t0035g0259 | 2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-54+633C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738985 | ||||||
chrX:15739450
|
G | GT | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0030g0257others(1): Show | 4 | HG00438.hp2 HG01358.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+1113dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15739450 | |||||
chrX:15739450
|
GT | G | 6 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0003g0062others(3): Show | 6 | HG01168.hp2 HG02630.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+1113delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15739450 | |||||
chrX:15739450
|
GTT | G | 32 | a0001c0001t0003g0004a0001c0001t0003g0029a0001c0001t0003g0032others(29): Show | 32 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-54+1112_-54+1113d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15739450 | |||||
chrX:15739450
|
GTTT | G | 1 | a0001c0001t0003g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-54+1111_-54+1113d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15739450 | |||||
chrX:15739795
|
GA | G | 2 | a0001c0001t0009g0056a0001c0001t0009g0057 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-54+1444delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15739795 | ||||||
chrX:15740026
|
GT | G | 1 | a0001c0001t0009g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-54+1676delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15740026 | |||||
chrX:15740123
|
C | T | 105 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(102): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-54+1771C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15740123 | ||||||
chrX:15740202
|
TC | T | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+1854delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15740202 | |||||
chrX:15740257
|
G | A | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-54+1905G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15740257 | ||||||
chrX:15740266
|
TC | T | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+1917delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15740266 | |||||
chrX:15740318
|
G | GT | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+1968dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15740318 | |||||
chrX:15740434
|
G | GC | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+2084dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15740434 | |||||
chrX:15740740
|
TC | T | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+2391delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15740740 | |||||
chrX:15740797
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-54+2445T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15740797 | ||||||
chrX:15741075
|
CT | C | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+2733delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741075 | |||||
chrX:15741142
|
A | AC | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+2791dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741142 | |||||
chrX:15741382
|
C | CA | 74 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0059others(71): Show | 74 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.-54+3051dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741382 | |||||
chrX:15741382
|
C | CAA | 1 | a0001c0001t0001g0066 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-54+3050_-54+3051d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741382 | |||||
chrX:15741382
|
CA | C | 5 | a0001c0001t0029g0055a0001c0001t0035g0259a0001c0002t0002g0250others(2): Show | 5 | HG02523.hp2 HG02723.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+3051delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741382 | |||||
chrX:15741492
|
T | G | 105 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(102): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-54+3140T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741492 | ||||||
chrX:15741510
|
T | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-54+3158T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741510 | ||||||
chrX:15741578
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-54+3226C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741578 | ||||||
chrX:15741729
|
GC | G | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+3379delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741729 | |||||
chrX:15741813
|
G | A | 1 | a0001c0001t0020g0097 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-54+3461G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741813 | ||||||
chrX:15741871
|
T | C | 8 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(5): Show | 8 | HG01071.hp2 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+3519T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741871 | ||||||
chrX:15741925
|
CT | C | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+3576delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741925 | |||||
chrX:15742234
|
TG | T | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+3884delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742234 | |||||
chrX:15742250
|
T | A | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+3898T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742250 | ||||||
chrX:15742265
|
AG | A | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+3916delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742265 | |||||
chrX:15742376
|
G | GT | 100 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0215others(97): Show | 105 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-54+4032dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742376 | |||||
chrX:15742390
|
G | A | 4 | a0001c0001t0008g0024a0001c0001t0010g0025a0001c0001t0010g0026others(1): Show | 4 | HG02280.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+4038G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742390 | ||||||
chrX:15742409
|
C | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-54+4057C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742409 | ||||||
chrX:15742409
|
C | G | 2 | a0001c0001t0012g0262a0001c0001t0012g0263 | 2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+4057C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742409 | ||||||
chrX:15742414
|
GC | G | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+4064delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742414 | |||||
chrX:15742452
|
C | CA | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+4102dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742452 | |||||
chrX:15742691
|
TA | T | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+4344delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742691 | |||||
chrX:15742751
|
C | G | 1 | a0001c0001t0015g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-54+4399C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742751 | ||||||
chrX:15742801
|
A | G | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-54+4449A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742801 | ||||||
chrX:15742960
|
C | G | 1 | a0001c0001t0003g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-54+4608C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742960 | ||||||
chrX:15742965
|
CA | C | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+4618delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742965 | |||||
chrX:15742996
|
C | T | 105 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(102): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-54+4644C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742996 | ||||||
chrX:15743184
|
GC | G | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+4834delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15743184 | |||||
chrX:15743475
|
AC | A | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+5125delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15743475 | |||||
chrX:15743526
|
CA | C | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+5179delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15743526 | |||||
chrX:15743564
|
G | A | 1 | a0001c0002t0007g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-54+5212G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743564 | ||||||
chrX:15743607
|
C | CA | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+5255_-54+5256i others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743607 | ||||||
chrX:15743746
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-54+5394G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743746 | ||||||
chrX:15743851
|
CT | C | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+5502delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15743851 | |||||
chrX:15743941
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-54+5589C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743941 | ||||||
chrX:15743955
|
C | A | 94 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(91): Show | 99 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-54+5603C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743955 | ||||||
chrX:15744143
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-54+5791T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744143 | ||||||
chrX:15744331
|
G | GA | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-53-5639dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15744331 | |||||
chrX:15744409
|
G | T | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-53-5562G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744409 | ||||||
chrX:15744431
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-53-5540C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744431 | ||||||
chrX:15744454
|
G | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-53-5517G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744454 | ||||||
chrX:15744551
|
G | A | 1 | a0001c0001t0031g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-53-5420G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744551 | ||||||
chrX:15744691
|
G | GC | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-53-5278dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15744691 | |||||
chrX:15745168
|
C | CA | 6 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0105others(3): Show | 6 | HG00323.hp1 HG04184.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-4784dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745168 | |||||
chrX:15745168
|
CA | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | NA18943.hp1 NA19072.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-53-4784delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745168 | |||||
chrX:15745183
|
A | AAAAAAAG | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-53-4784_-53-4783i others(9): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | |||||
chrX:15745183
|
A | AAAAAAG | 15 | a0001c0001t0003g0029a0001c0001t0005g0070a0001c0001t0008g0024others(12): Show | 16 | HG01928.hp1 HG02080.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53-4784_-53-4783i others(8): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | |||||
chrX:15745183
|
A | AAAAAG | 111 | a0001c0001t0001g0006a0001c0001t0001g0156a0001c0001t0001g0181others(108): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-53-4763_-53-4759d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | |||||
chrX:15745183
|
A | AAAAAGAA others(3): Show |
1 | a0001c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-53-4768_-53-4759d others(12): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | |||||
chrX:15745183
|
A | AAAAG | 1 | a0001c0001t0014g0248 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53-4785_-53-4784i others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | |||||
chrX:15745183
|
AAAAAG | A | 9 | a0001c0001t0001g0096a0001c0001t0001g0161a0001c0001t0012g0262others(6): Show | 9 | HG01071.hp2 HG02074.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-4763_-53-4759d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | |||||
chrX:15745417
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-53-4554G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15745417 | ||||||
chrX:15745715
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-53-4256G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15745715 | ||||||
chrX:15745845
|
AT | A | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-53-4125delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15745845 | ||||||
chrX:15745906
|
A | T | 1 | a0001c0002t0002g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-53-4065A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15745906 | ||||||
chrX:15746022
|
C | CT | 51 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(48): Show | 53 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-53-3924dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746022 | |||||
chrX:15746022
|
C | CTT | 1 | a0001c0001t0001g0021 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-53-3925_-53-3924d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746022 | |||||
chrX:15746022
|
CT | C | 44 | a0001c0001t0001g0110a0001c0001t0001g0157a0001c0001t0001g0261others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-53-3924delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746022 | |||||
chrX:15746022
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0008g0039a0001c0001t0008g0040 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-53-3936_-53-3924d others(15): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746022 | |||||
chrX:15746047
|
T | A | 1 | a0001c0001t0003g0044 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-53-3924T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746047 | ||||||
chrX:15746056
|
GTCTCGCT others(1): Show |
G | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-53-3913_-53-3906d others(10): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746056 | |||||
chrX:15746061
|
GCTCTGTC others(1): Show |
G | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(258): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-53-3898_-53-3891d others(10): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746061 | |||||
chrX:15746069
|
A | G | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-53-3902A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746069 | ||||||
chrX:15746079
|
T | C | 136 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(133): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-53-3892T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746079 | ||||||
chrX:15746148
|
C | T | 136 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(133): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-53-3823C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746148 | ||||||
chrX:15746324
|
C | T | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-53-3647C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746324 | ||||||
chrX:15746354
|
G | A | 10 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-53-3617G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746354 | ||||||
chrX:15746461
|
A | G | 136 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(133): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-53-3510A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746461 | ||||||
chrX:15746593
|
G | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-3378G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746593 | ||||||
chrX:15746698
|
G | A | 1 | a0001c0001t0008g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-53-3273G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746698 | ||||||
chrX:15746886
|
C | A | 1 | a0001c0001t0003g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-53-3085C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746886 | ||||||
chrX:15747025
|
G | A | 2 | a0001c0001t0012g0262a0001c0001t0012g0263 | 2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-2946G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747025 | ||||||
chrX:15747071
|
T | C | 1 | a0001c0002t0002g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-2900T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747071 | ||||||
chrX:15747073
|
T | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0061others(39): Show | 43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-53-2898T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747073 | ||||||
chrX:15747121
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-53-2850A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747121 | ||||||
chrX:15747519
|
G | T | 1 | a0001c0001t0003g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-53-2452G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747519 | ||||||
chrX:15747592
|
A | G | 154 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(151): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-53-2379A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747592 | ||||||
chrX:15747808
|
C | A | 4 | a0001c0001t0008g0024a0001c0001t0010g0025a0001c0001t0010g0026others(1): Show | 4 | HG02280.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-2163C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747808 | ||||||
chrX:15747899
|
A | AGAGAGGA others(19): Show |
6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-2054_-53-2029d others(28): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15747899 | |||||
chrX:15747899
|
AGAGAGGA others(19): Show |
A | 1 | a0001c0001t0008g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-53-2054_-53-2029d others(28): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15747899 | |||||
chrX:15748044
|
C | G | 1 | a0001c0001t0001g0125 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-53-1927C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748044 | ||||||
chrX:15748054
|
C | T | 2 | a0001c0001t0012g0262a0001c0001t0012g0263 | 2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-1917C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748054 | ||||||
chrX:15748197
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-53-1774G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748197 | ||||||
chrX:15748511
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0005g0068 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-53-1460A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748511 | ||||||
chrX:15748641
|
G | A | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-1330G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748641 | ||||||
chrX:15748708
|
A | AC | 80 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0066others(77): Show | 82 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-53-1252dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | |||||
chrX:15748708
|
A | ACC | 25 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0082others(22): Show | 25 | HG01106.hp1 HG01891.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.-53-1253_-53-1252d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | |||||
chrX:15748708
|
A | ACCC | 1 | a0001c0001t0005g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-53-1254_-53-1252d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | |||||
chrX:15748708
|
A | ACCCC | 1 | a0001c0001t0001g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53-1255_-53-1252d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | |||||
chrX:15748708
|
AC | A | 16 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG01071.hp2 HG01346.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-53-1252delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | |||||
chrX:15748708
|
ACC | A | 26 | a0001c0001t0003g0004a0001c0001t0003g0028a0001c0001t0003g0029others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.-53-1253_-53-1252d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | |||||
chrX:15748720
|
G | A | 6 | a0001c0001t0008g0024a0001c0001t0010g0025a0001c0001t0010g0026others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53-1251G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748720 | ||||||
chrX:15748820
|
TG | T | 1 | a0001c0002t0002g0239 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-53-1148delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748820 | |||||
chrX:15748836
|
G | A | 1 | a0001c0001t0016g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-53-1135G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748836 | ||||||
chrX:15749152
|
G | GT | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-819_-53-818ins others(1): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749152 | ||||||
chrX:15749153
|
A | T | 8 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(5): Show | 8 | HG01071.hp2 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-818A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749153 | ||||||
chrX:15749153
|
AT | A | 2 | a0001c0002t0002g0193a0001c0002t0002g0200 | 2 | HG01515.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-53-806delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15749153 | |||||
chrX:15749178
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-53-793A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749178 | ||||||
chrX:15749506
|
G | GT | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-53-458dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15749506 | |||||
chrX:15749511
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53-460T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749511 | ||||||
chrX:15749514
|
G | T | 2 | a0001c0002t0002g0182a0001c0002t0002g0238 | 2 | NA18941.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-53-457G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749514 | ||||||
chrX:15749596
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0255 | 3 | HG00438.hp2 HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-53-375G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749596 | ||||||
chrX:15749644
|
A | AT | 3 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041 | 3 | HG01884.hp1 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-53-314dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15749644 | |||||
chrX:15749644
|
AT | A | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0157others(4): Show | 7 | HG02965.hp1 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-314delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15749644 | |||||
chrX:15749734
|
AC | A | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-53-234delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15749734 | |||||
chrX:15750254
|
GA | G | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+93delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15750254 | |||||
chrX:15750270
|
T | C | 10 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+105T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15750270 | ||||||
chrX:15750447
|
G | GT | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+284dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15750447 | |||||
chrX:15750509
|
C | A | 1 | a0001c0002t0002g0241 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.142+344C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15750509 | ||||||
chrX:15750541
|
CT | C | 1 | a0001c0001t0001g0149 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.142+387delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15750541 | |||||
chrX:15750557
|
TA | T | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+395delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15750557 | |||||
chrX:15750990
|
T | TC | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+826dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15750990 | |||||
chrX:15751017
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.142+852C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751017 | ||||||
chrX:15751539
|
C | CT | 11 | a0001c0001t0005g0070a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+1387dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15751539 | |||||
chrX:15751539
|
CT | C | 2 | a0001c0002t0002g0211a0001c0002t0002g0212 | 2 | NA18962.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.142+1387delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15751539 | |||||
chrX:15751624
|
C | CA | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+1468dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15751624 | |||||
chrX:15751667
|
C | G | 4 | a0001c0001t0009g0031a0001c0001t0009g0056a0001c0001t0009g0057others(1): Show | 4 | HG01884.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+1502C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751667 | ||||||
chrX:15751667
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.142+1502C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751667 | ||||||
chrX:15751758
|
A | G | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.142+1593A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751758 | ||||||
chrX:15751796
|
A | G | 1 | a0001c0002t0004g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.142+1631A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751796 | ||||||
chrX:15751829
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.142+1664G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751829 | ||||||
chrX:15751974
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0106 | 2 | NA18961.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.142+1809C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751974 | ||||||
chrX:15751983
|
G | GA | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+1824dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15751983 | |||||
chrX:15752132
|
G | A | 10 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+1967G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752132 | ||||||
chrX:15752174
|
C | T | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.142+2009C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752174 | ||||||
chrX:15752184
|
A | AT | 10 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0008g0041others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+2029dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752184 | |||||
chrX:15752220
|
G | A | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2055G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752220 | ||||||
chrX:15752235
|
GC | G | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+2074delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752235 | |||||
chrX:15752288
|
G | A | 2 | a0001c0001t0003g0046a0001c0001t0003g0062 | 2 | NA18946.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.142+2123G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752288 | ||||||
chrX:15752296
|
CT | C | 1 | a0001c0001t0001g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.142+2134delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752296 | |||||
chrX:15752320
|
C | G | 1 | a0001c0001t0034g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142+2155C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752320 | ||||||
chrX:15752451
|
C | T | 1 | a0001c0001t0031g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142+2286C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752451 | ||||||
chrX:15752461
|
T | C | 4 | a0001c0001t0003g0032a0001c0002t0002g0166a0001c0002t0002g0211others(1): Show | 4 | HG01175.hp1 HG02080.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+2296T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752461 | ||||||
chrX:15752485
|
C | G | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+2320C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752485 | ||||||
chrX:15752496
|
C | CG | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+2334dupG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752496 | |||||
chrX:15752500
|
C | T | 14 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+2335C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752500 | ||||||
chrX:15752522
|
A | G | 8 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(5): Show | 8 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+2357A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752522 | ||||||
chrX:15752527
|
T | C | 154 | a0001c0001t0001g0181a0001c0001t0001g0215a0001c0001t0001g0216others(151): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.142+2362T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752527 | ||||||
chrX:15752528
|
A | G | 1 | a0001c0001t0003g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.142+2363A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752528 | ||||||
chrX:15752537
|
A | AAC | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(105): Show | 112 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.142+2375_142+2376d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752537 | |||||
chrX:15752542
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(105): Show | 112 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.142+2377G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752542 | ||||||
chrX:15752582
|
A | G | 1 | a0004c0003t0007g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.142+2417A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752582 | ||||||
chrX:15752585
|
C | T | 2 | a0001c0001t0012g0262a0001c0001t0012g0263 | 2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142+2420C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752585 | ||||||
chrX:15752593
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0016g0022 | 2 | HG02717.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.142+2428T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752593 | ||||||
chrX:15752617
|
A | T | 1 | a0001c0002t0002g0166 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.142+2452A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752617 | ||||||
chrX:15752618
|
A | G | 1 | a0001c0002t0002g0166 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.142+2453A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752618 | ||||||
chrX:15752622
|
T | G | 2 | a0001c0001t0006g0099a0001c0002t0002g0166 | 2 | HG02080.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.142+2457T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752622 | ||||||
chrX:15752632
|
T | G | 7 | a0001c0001t0006g0099a0001c0001t0013g0249a0001c0001t0013g0258others(4): Show | 7 | HG02080.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+2467T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752632 | ||||||
chrX:15752642
|
G | A | 10 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+2477G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752642 | ||||||
chrX:15752654
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.142+2489G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752654 | ||||||
chrX:15752669
|
G | A | 1 | a0001c0002t0002g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142+2504G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752669 | ||||||
chrX:15752673
|
C | T | 3 | a0001c0001t0013g0249a0001c0001t0013g0258a0001c0001t0035g0259 | 3 | HG02965.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.142+2508C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752673 | ||||||
chrX:15752674
|
G | A | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2509G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752674 | ||||||
chrX:15752681
|
C | T | 93 | a0001c0001t0001g0181a0001c0001t0001g0243a0001c0002t0002g0001others(90): Show | 98 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.142+2516C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752681 | ||||||
chrX:15752682
|
G | A | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2517G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752682 | ||||||
chrX:15752702
|
G | A | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2537G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752702 | ||||||
chrX:15752703
|
C | T | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2538C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752703 | ||||||
chrX:15752704
|
G | A | 1 | a0001c0001t0010g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.142+2539G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752704 | ||||||
chrX:15752716
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142+2551C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752716 | ||||||
chrX:15752719
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0003g0160 | 2 | HG01934.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.142+2554T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752719 | ||||||
chrX:15752720
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142+2555G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752720 | ||||||
chrX:15752724
|
C | CA | 4 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0138others(1): Show | 4 | HG03098.hp1 NA18944.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+2573dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752724 | |||||
chrX:15752724
|
CA | C | 103 | a0001c0001t0001g0181a0001c0001t0001g0243a0001c0001t0001g0261others(100): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.142+2573delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752724 | |||||
chrX:15752851
|
A | G | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142+2686A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752851 | ||||||
chrX:15752914
|
C | G | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+2749C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752914 | ||||||
chrX:15752987
|
G | GC | 13 | a0001c0001t0001g0082a0001c0001t0001g0092a0001c0001t0001g0095others(10): Show | 13 | HG01071.hp2 HG01496.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+2829dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752987 | |||||
chrX:15752993
|
C | G | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+2828C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752993 | ||||||
chrX:15752994
|
C | T | 1 | a0001c0001t0005g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142+2829C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752994 | ||||||
chrX:15753040
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.142+2875C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753040 | ||||||
chrX:15753501
|
T | C | 1 | a0001c0002t0026g0172 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.142+3336T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753501 | ||||||
chrX:15753632
|
G | C | 2 | a0001c0001t0011g0126a0001c0001t0011g0139 | 2 | HG02293.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.142+3467G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753632 | ||||||
chrX:15753665
|
T | G | 4 | a0001c0002t0002g0217a0001c0002t0002g0242a0001c0002t0004g0185others(1): Show | 4 | HG02109.hp2 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+3500T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753665 | ||||||
chrX:15753707
|
G | A | 1 | a0001c0002t0027g0219 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+3542G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753707 | ||||||
chrX:15753773
|
G | C | 1 | a0001c0001t0009g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+3608G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753773 | ||||||
chrX:15753894
|
GA | G | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+3730delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753894 | ||||||
chrX:15753917
|
T | C | 1 | a0001c0001t0031g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142+3752T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753917 | ||||||
chrX:15753932
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.142+3767C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753932 | ||||||
chrX:15754349
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.142+4184G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15754349 | ||||||
chrX:15754462
|
G | C | 1 | a0001c0001t0003g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142+4297G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15754462 | ||||||
chrX:15754776
|
G | A | 1 | a0001c0001t0008g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.142+4611G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15754776 | ||||||
chrX:15755357
|
A | G | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142+5192A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755357 | ||||||
chrX:15755362
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0005g0068 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.142+5197A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755362 | ||||||
chrX:15755372
|
A | G | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+5207A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755372 | ||||||
chrX:15755385
|
T | G | 6 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0127others(3): Show | 6 | HG02145.hp1 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+5220T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755385 | ||||||
chrX:15755443
|
TC | T | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+5281delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15755443 | |||||
chrX:15755590
|
TC | T | 1 | a0001c0002t0002g0210 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.142+5427delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15755590 | |||||
chrX:15755686
|
AG | A | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+5523delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15755686 | |||||
chrX:15755744
|
TG | T | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+5582delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15755744 | |||||
chrX:15755820
|
G | A | 34 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.142+5655G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755820 | ||||||
chrX:15755879
|
A | AC | 1 | a0001c0002t0002g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+5716dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15755879 | |||||
chrX:15756210
|
A | G | 1 | a0001c0002t0002g0192 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.142+6045A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756210 | ||||||
chrX:15756469
|
TA | T | 1 | a0001c0001t0034g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142+6307delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15756469 | |||||
chrX:15756619
|
T | TG | 1 | a0001c0002t0002g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.142+6458dupG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15756619 | |||||
chrX:15756754
|
T | A | 2 | a0001c0002t0004g0201a0001c0002t0004g0202 | 2 | NA19005.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.142+6589T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756754 | ||||||
chrX:15756776
|
C | T | 1 | a0001c0002t0002g0236 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.142+6611C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756776 | ||||||
chrX:15756783
|
A | G | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+6618A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756783 | ||||||
chrX:15756792
|
T | C | 4 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(1): Show | 4 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+6627T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756792 | ||||||
chrX:15757054
|
C | CA | 33 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(30): Show | 33 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.142+6906dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757054 | |||||
chrX:15757054
|
C | CAA | 6 | a0001c0001t0003g0029a0001c0001t0003g0044a0001c0001t0003g0046others(3): Show | 6 | HG00741.hp1 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+6905_142+6906d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757054 | |||||
chrX:15757054
|
C | CAAA | 1 | a0001c0001t0003g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.142+6904_142+6906d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757054 | |||||
chrX:15757054
|
CA | C | 2 | a0001c0001t0001g0092a0001c0002t0024g0196 | 2 | NA18992.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.142+6906delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757054 | |||||
chrX:15757147
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.142+6982G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15757147 | ||||||
chrX:15757407
|
G | A | 29 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-7171G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15757407 | ||||||
chrX:15757665
|
GC | G | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-6911delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757665 | |||||
chrX:15757707
|
C | CA | 31 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0066others(28): Show | 31 | HG00438.hp1 HG00741.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-6855dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757707 | |||||
chrX:15757707
|
C | CAA | 1 | a0001c0001t0001g0083 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.143-6856_143-6855d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757707 | |||||
chrX:15757707
|
CA | C | 21 | a0001c0001t0001g0082a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 21 | HG01496.hp2 HG02165.hp2 HG03710.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-6855delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757707 | |||||
chrX:15757761
|
G | A | 98 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0002t0002g0001others(95): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.143-6817G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15757761 | ||||||
chrX:15757882
|
TG | T | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-6693delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757882 | |||||
chrX:15758048
|
A | AG | 1 | a0001c0002t0002g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.143-6527dupG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15758048 | |||||
chrX:15758243
|
G | A | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-6335G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758243 | ||||||
chrX:15758278
|
T | C | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-6300T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758278 | ||||||
chrX:15758461
|
G | A | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-6117G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758461 | ||||||
chrX:15758518
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.143-6060A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758518 | ||||||
chrX:15758599
|
C | T | 1 | a0001c0001t0016g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.143-5979C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758599 | ||||||
chrX:15758968
|
C | T | 1 | a0001c0002t0002g0171 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.143-5610C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758968 | ||||||
chrX:15759013
|
TA | T | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-5560delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759013 | |||||
chrX:15759114
|
C | T | 106 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0001t0012g0262others(103): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.143-5464C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759114 | ||||||
chrX:15759182
|
GGAA | G | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-5395_143-5393d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759182 | ||||||
chrX:15759240
|
T | TAGG | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-5337_143-5335d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759240 | |||||
chrX:15759418
|
G | A | 1 | a0001c0002t0002g0239 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.143-5160G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759418 | ||||||
chrX:15759645
|
A | T | 97 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0002t0002g0001others(94): Show | 102 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.143-4933A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759645 | ||||||
chrX:15759651
|
A | G | 2 | a0001c0001t0003g0032a0001c0001t0003g0052 | 2 | HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.143-4927A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759651 | ||||||
chrX:15759688
|
T | TC | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-4888dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759688 | |||||
chrX:15759734
|
C | CTT | 1 | a0001c0001t0010g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.143-4813_143-4812d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
C | CTTT | 5 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(2): Show | 5 | HG01884.hp1 HG02647.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4814_143-4812d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
C | CTTTT | 6 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0103others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-4815_143-4812d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
C | CTTTTT | 5 | a0001c0001t0008g0039a0001c0001t0009g0031a0001c0001t0009g0056others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-4816_143-4812d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
C | CTTTTTT | 3 | a0001c0001t0008g0041a0001c0001t0008g0042a0001c0001t0008g0043 | 3 | HG02280.hp2 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.143-4817_143-4812d others(8): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
CT | C | 10 | a0001c0001t0001g0138a0001c0001t0003g0033a0001c0001t0003g0037others(7): Show | 10 | HG00741.hp1 HG01192.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-4812delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
CTT | C | 29 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0106others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-4813_143-4812d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
CTTT | C | 69 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(66): Show | 69 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.143-4814_143-4812d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
CTTTT | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(121): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.143-4815_143-4812d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759734
|
CTTTTT | C | 7 | a0001c0001t0005g0086a0001c0001t0013g0249a0001c0001t0013g0258others(4): Show | 7 | HG01257.hp1 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-4816_143-4812d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | |||||
chrX:15759874
|
TC | T | 1 | a0001c0002t0002g0183 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.143-4701delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759874 | |||||
chrX:15759928
|
A | G | 1 | a0001c0001t0009g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.143-4650A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759928 | ||||||
chrX:15759942
|
T | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.143-4636T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759942 | ||||||
chrX:15759966
|
C | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0125 | 2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.143-4612C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759966 | ||||||
chrX:15759973
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0125 | 2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.143-4605T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759973 | ||||||
chrX:15759974
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0125 | 2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.143-4604G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759974 | ||||||
chrX:15760032
|
G | A | 1 | a0001c0001t0010g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.143-4546G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760032 | ||||||
chrX:15760097
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.143-4481A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760097 | ||||||
chrX:15760111
|
T | C | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-4467T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760111 | ||||||
chrX:15760201
|
T | TC | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-4377_143-4376i others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760201 | ||||||
chrX:15760563
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.143-4015G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760563 | ||||||
chrX:15760595
|
A | C | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-3983A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760595 | ||||||
chrX:15760635
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.143-3943A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760635 | ||||||
chrX:15760668
|
C | G | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-3910C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760668 | ||||||
chrX:15760672
|
T | C | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-3906T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760672 | ||||||
chrX:15760880
|
T | TC | 1 | a0001c0002t0007g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.143-3691dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15760880 | |||||
chrX:15760925
|
ATTTTATT | A | 1 | a0001c0001t0001g0014 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.143-3642_143-3636d others(9): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15760925 | |||||
chrX:15760987
|
G | GT | 1 | a0001c0001t0001g0157 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.143-3588dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15760987 | |||||
chrX:15761031
|
T | C | 2 | a0001c0002t0002g0182a0001c0002t0002g0238 | 2 | NA18941.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.143-3547T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761031 | ||||||
chrX:15761058
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(8): Show | 13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3520C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761058 | ||||||
chrX:15761088
|
C | T | 9 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-3490C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761088 | ||||||
chrX:15761179
|
C | CT | 29 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-3393dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15761179 | |||||
chrX:15761179
|
CT | C | 2 | a0001c0001t0001g0082a0001c0002t0002g0210 | 2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.143-3393delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15761179 | |||||
chrX:15761402
|
G | A | 3 | a0001c0001t0013g0249a0001c0001t0013g0258a0001c0001t0030g0257 | 3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.143-3176G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761402 | ||||||
chrX:15761564
|
A | G | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-3014A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761564 | ||||||
chrX:15761721
|
C | CG | 2 | a0001c0001t0001g0123a0001c0001t0003g0051 | 2 | HG03834.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.143-2851dupG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15761721 | |||||
chrX:15761721
|
CG | C | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-2851delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15761721 | |||||
chrX:15761841
|
A | G | 7 | a0001c0001t0001g0082a0001c0001t0001g0124a0001c0001t0001g0143others(4): Show | 7 | HG01496.hp2 HG02148.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-2737A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761841 | ||||||
chrX:15761985
|
C | T | 9 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-2593C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761985 | ||||||
chrX:15762129
|
G | A | 29 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-2449G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762129 | ||||||
chrX:15762146
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-2432T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762146 | ||||||
chrX:15762268
|
T | TA | 2 | a0001c0001t0003g0037a0001c0002t0002g0221 | 2 | NA18989.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.143-2297dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15762268 | |||||
chrX:15762268
|
TA | T | 2 | a0001c0002t0002g0234a0001c0002t0004g0232 | 2 | NA18940.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.143-2297delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15762268 | |||||
chrX:15762294
|
C | A | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-2284C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762294 | ||||||
chrX:15762370
|
T | C | 1 | a0001c0002t0002g0222 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.143-2208T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762370 | ||||||
chrX:15762425
|
A | G | 105 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0001t0012g0262others(102): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.143-2153A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762425 | ||||||
chrX:15762442
|
C | G | 1 | a0001c0001t0003g0051 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.143-2136C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762442 | ||||||
chrX:15762448
|
CT | C | 1 | a0001c0001t0005g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.143-2119delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15762448 | |||||
chrX:15762503
|
G | A | 1 | a0001c0002t0026g0172 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.143-2075G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762503 | ||||||
chrX:15762524
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0005g0121a0001c0002t0024g0196 | 3 | NA19056.hp1 NA19086.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.143-2054C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762524 | ||||||
chrX:15762534
|
C | T | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-2044C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762534 | ||||||
chrX:15762576
|
G | A | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.143-2002G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762576 | ||||||
chrX:15762641
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.143-1937G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762641 | ||||||
chrX:15762728
|
T | C | 6 | a0001c0001t0003g0029a0001c0001t0003g0044a0001c0001t0003g0046others(3): Show | 6 | NA18942.hp1 NA18946.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-1850T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762728 | ||||||
chrX:15763103
|
A | G | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-1475A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763103 | ||||||
chrX:15763282
|
G | A | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.143-1296G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763282 | ||||||
chrX:15763542
|
C | T | 1 | a0001c0002t0027g0219 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.143-1036C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763542 | ||||||
chrX:15763592
|
C | G | 157 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(154): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.143-986C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763592 | ||||||
chrX:15763876
|
G | A | 1 | a0001c0002t0007g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.143-702G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763876 | ||||||
chrX:15763908
|
C | G | 1 | a0001c0001t0008g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143-670C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763908 | ||||||
chrX:15764201
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.143-377T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764201 | ||||||
chrX:15764274
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.143-304G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764274 | ||||||
chrX:15764320
|
A | G | 106 | a0001c0001t0001g0136a0001c0001t0005g0067a0001c0001t0005g0086others(103): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.143-258A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764320 | ||||||
chrX:15764327
|
C | T | 39 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.143-251C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764327 | ||||||
chrX:15764440
|
G | A | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-138G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764440 | ||||||
chrX:15765611
|
T | A | 1 | a0001c0002t0002g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.340+836T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15765611 | ||||||
chrX:15765644
|
C | T | 6 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0104others(3): Show | 6 | HG02523.hp1 NA18942.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+869C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15765644 | ||||||
chrX:15766155
|
CA | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.340+1403delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15766155 | |||||
chrX:15766155
|
CAA | C | 94 | a0001c0001t0001g0120a0001c0001t0001g0158a0001c0001t0003g0037others(91): Show | 99 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.340+1402_340+1403d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15766155 | |||||
chrX:15766155
|
CAAA | C | 11 | a0001c0002t0002g0009a0001c0002t0002g0167a0001c0002t0002g0169others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.340+1401_340+1403d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15766155 | |||||
chrX:15766375
|
A | G | 8 | a0001c0001t0001g0136a0001c0001t0012g0262a0001c0001t0012g0263others(5): Show | 8 | HG01071.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+1600A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15766375 | ||||||
chrX:15767289
|
T | C | 4 | a0001c0001t0003g0028a0001c0001t0003g0033a0001c0001t0003g0036others(1): Show | 4 | HG00323.hp2 HG01192.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+2514T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767289 | ||||||
chrX:15767404
|
A | AT | 8 | a0001c0001t0001g0122a0001c0001t0006g0098a0001c0001t0006g0099others(5): Show | 8 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+2644dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767404 | |||||
chrX:15767404
|
AT | A | 3 | a0001c0001t0001g0110a0001c0001t0003g0028a0001c0001t0003g0036 | 3 | HG00323.hp2 HG01257.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.340+2644delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767404 | |||||
chrX:15767424
|
CAG | C | 1 | a0001c0002t0002g0251 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.340+2652_340+2653d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767424 | |||||
chrX:15767468
|
T | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.340+2693T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767468 | ||||||
chrX:15767535
|
G | A | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.340+2760G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767535 | ||||||
chrX:15767770
|
A | G | 1 | a0004c0003t0007g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.340+2995A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767770 | ||||||
chrX:15767810
|
G | A | 29 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.340+3035G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767810 | ||||||
chrX:15767849
|
C | T | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+3074C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767849 | ||||||
chrX:15767897
|
C | CT | 126 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0001t0001g0095others(123): Show | 131 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.340+3141dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767897 | |||||
chrX:15767897
|
C | CTT | 9 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0177others(6): Show | 9 | HG00438.hp1 HG01109.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+3140_340+3141d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767897 | |||||
chrX:15767897
|
C | CTTTT | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.340+3138_340+3141d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767897 | |||||
chrX:15767897
|
CT | C | 4 | a0001c0001t0001g0078a0001c0001t0001g0127a0001c0001t0001g0134others(1): Show | 4 | HG02976.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+3141delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767897 | |||||
chrX:15767904
|
T | TTG | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.340+3130_340+3131i others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767904 | |||||
chrX:15767938
|
G | A | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.340+3163G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767938 | ||||||
chrX:15767974
|
C | T | 1 | a0001c0002t0007g0206 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.340+3199C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767974 | ||||||
chrX:15767986
|
C | T | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.340+3211C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767986 | ||||||
chrX:15768010
|
C | T | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.340+3235C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768010 | ||||||
chrX:15768176
|
T | C | 118 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0001t0006g0098others(115): Show | 123 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.340+3401T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768176 | ||||||
chrX:15768410
|
A | G | 1 | a0001c0001t0009g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.340+3635A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768410 | ||||||
chrX:15768606
|
T | C | 1 | a0001c0001t0011g0139 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.340+3831T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768606 | ||||||
chrX:15768606
|
T | TTC | 1 | a0001c0001t0013g0258 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.340+3851_340+3852d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15768606 | |||||
chrX:15768606
|
TTC | T | 1 | a0001c0001t0013g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.340+3851_340+3852d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15768606 | |||||
chrX:15768623
|
TCTC | T | 1 | a0001c0001t0014g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.340+3849_340+3851d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768623 | ||||||
chrX:15768752
|
A | G | 2 | a0001c0001t0009g0056a0001c0001t0009g0057 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.341-3744A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768752 | ||||||
chrX:15769229
|
A | G | 98 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0002t0002g0001others(95): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.341-3267A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769229 | ||||||
chrX:15769624
|
T | A | 1 | a0001c0002t0002g0198 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.341-2872T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769624 | ||||||
chrX:15769701
|
C | G | 6 | a0001c0002t0007g0165a0001c0002t0007g0206a0001c0002t0007g0231others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-2795C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769701 | ||||||
chrX:15769706
|
T | G | 2 | a0001c0001t0001g0073a0002c0006t0001g0119 | 2 | HG00597.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.341-2790T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769706 | ||||||
chrX:15769828
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.341-2668G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769828 | ||||||
chrX:15770188
|
C | T | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.341-2308C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770188 | ||||||
chrX:15770205
|
T | C | 148 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(145): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.341-2291T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770205 | ||||||
chrX:15770262
|
C | CG | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.341-2233dupG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770262 | |||||
chrX:15770324
|
T | TA | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.341-2166dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770324 | |||||
chrX:15770417
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.341-2079A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770417 | ||||||
chrX:15770444
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.341-2052T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770444 | ||||||
chrX:15770468
|
A | AG | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.341-2027dupG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770468 | |||||
chrX:15770710
|
A | AC | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.341-1785dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770710 | |||||
chrX:15770719
|
T | TTC | 1 | a0001c0001t0001g0243 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.341-1763_341-1762d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770719 | |||||
chrX:15770731
|
CTCTT | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0156 | 3 | HG01069.hp1 HG01071.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.341-1754_341-1751d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770731 | |||||
chrX:15770733
|
CTT | C | 82 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0002t0002g0001others(79): Show | 87 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.341-1761_341-1760d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770733 | |||||
chrX:15770829
|
G | A | 2 | a0001c0001t0012g0262a0001c0001t0012g0263 | 2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.341-1667G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770829 | ||||||
chrX:15770932
|
T | A | 4 | a0001c0001t0009g0031a0001c0001t0009g0056a0001c0001t0009g0057others(1): Show | 4 | HG01884.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1564T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770932 | ||||||
chrX:15771084
|
G | T | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.341-1412G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771084 | ||||||
chrX:15771201
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.341-1295C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771201 | ||||||
chrX:15771204
|
C | CA | 10 | a0001c0001t0001g0071a0001c0001t0001g0118a0001c0001t0001g0122others(7): Show | 10 | HG02083.hp1 HG02280.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-1272dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771204 | |||||
chrX:15771204
|
C | CAA | 94 | a0001c0001t0001g0254a0001c0001t0005g0067a0001c0001t0005g0086others(91): Show | 98 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.341-1273_341-1272d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771204 | |||||
chrX:15771204
|
C | CAAA | 12 | a0001c0001t0030g0257a0001c0002t0002g0008a0001c0002t0002g0009others(9): Show | 13 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.341-1274_341-1272d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771204 | |||||
chrX:15771370
|
C | CA | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.341-1113dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771370 | |||||
chrX:15771370
|
CA | C | 150 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(147): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.341-1113delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771370 | |||||
chrX:15771370
|
CAAAAAA | C | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.341-1118_341-1113d others(8): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771370 | |||||
chrX:15771423
|
T | TTG | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-1055_341-1054d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771423 | |||||
chrX:15771435
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-1061G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771435 | ||||||
chrX:15771593
|
A | AT | 39 | a0001c0001t0001g0074a0001c0001t0003g0004a0001c0001t0003g0011others(36): Show | 39 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.341-886dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771593 | |||||
chrX:15771593
|
AT | A | 6 | a0001c0001t0001g0061a0001c0001t0015g0023a0001c0001t0016g0022others(3): Show | 6 | HG01168.hp2 HG02523.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-886delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771593 | |||||
chrX:15771610
|
T | A | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-886T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771610 | ||||||
chrX:15771769
|
C | T | 157 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(154): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.341-727C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771769 | ||||||
chrX:15771864
|
A | AT | 44 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0082others(41): Show | 44 | HG01069.hp1 HG01106.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.341-621dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771864 | |||||
chrX:15771864
|
A | ATT | 1 | a0001c0001t0018g0081 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.341-622_341-621dup others(2): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771864 | |||||
chrX:15771864
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.341-632A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771864 | ||||||
chrX:15772124
|
A | G | 3 | a0001c0001t0013g0249a0001c0001t0013g0258a0001c0001t0030g0257 | 3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.341-372A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15772124 | ||||||
chrX:15772210
|
A | G | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.341-286A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15772210 | ||||||
chrX:15772263
|
G | T | 1 | a0001c0001t0013g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.341-233G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15772263 | ||||||
chrX:15772656
|
TG | T | 1 | a0001c0002t0002g0210 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.459+46delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15772656 | |||||
chrX:15772711
|
A | G | 1 | a0001c0001t0010g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.459+97A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772711 | ||||||
chrX:15772719
|
TA | T | 1 | a0001c0002t0002g0210 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.459+108delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15772719 | |||||
chrX:15772890
|
A | G | 2 | a0001c0001t0008g0042a0001c0001t0008g0043 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.459+276A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772890 | ||||||
chrX:15772926
|
G | T | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.459+312G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772926 | ||||||
chrX:15772957
|
A | G | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.459+343A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772957 | ||||||
chrX:15773054
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.459+440G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773054 | ||||||
chrX:15773099
|
A | G | 1 | a0001c0002t0002g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.459+485A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773099 | ||||||
chrX:15773110
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.459+496A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773110 | ||||||
chrX:15773212
|
T | TA | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.459+605dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15773212 | |||||
chrX:15773274
|
T | G | 4 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(1): Show | 4 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+660T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773274 | ||||||
chrX:15773345
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0005g0070 | 2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.459+731G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773345 | ||||||
chrX:15773385
|
A | G | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.459+771A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773385 | ||||||
chrX:15773402
|
AT | A | 22 | a0001c0001t0001g0094a0001c0001t0001g0130a0001c0001t0001g0150others(19): Show | 22 | HG00597.hp1 HG01109.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+813delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15773402 | |||||
chrX:15773402
|
ATT | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.459+812_459+813del others(2): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15773402 | |||||
chrX:15773402
|
ATTT | A | 1 | a0001c0001t0001g0087 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.459+811_459+813del others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15773402 | |||||
chrX:15773402
|
ATTTTT | A | 2 | a0001c0002t0002g0203a0001c0002t0002g0229 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.459+809_459+813del others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15773402 | |||||
chrX:15773425
|
TTTG | T | 1 | a0001c0001t0001g0061 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.459+812_459+814del others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773425 | ||||||
chrX:15773534
|
C | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0125 | 2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.460-768C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773534 | ||||||
chrX:15773552
|
A | G | 1 | a0001c0002t0002g0175 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.460-750A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773552 | ||||||
chrX:15773661
|
G | A | 1 | a0001c0001t0003g0013 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.460-641G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773661 | ||||||
chrX:15773667
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0120 | 2 | HG01168.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.460-635C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773667 | ||||||
chrX:15773688
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.460-614C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773688 | ||||||
chrX:15773771
|
C | T | 1 | a0001c0001t0030g0257 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.460-531C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773771 | ||||||
chrX:15773870
|
A | T | 1 | a0001c0002t0002g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.460-432A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773870 | ||||||
chrX:15773943
|
A | G | 1 | a0001c0001t0031g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.460-359A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773943 | ||||||
chrX:15773975
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0255 | 3 | HG00438.hp2 HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.460-327G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773975 | ||||||
chrX:15774012
|
G | A | 11 | a0001c0001t0008g0024a0001c0001t0008g0039a0001c0001t0008g0040others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-290G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15774012 | ||||||
chrX:15774253
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-49G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15774253 | ||||||
chrX:15774404
|
T | A | 157 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(154): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
splice_region_variant&intron_variant | LOW | c.555+7T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774404 | ||||||
chrX:15774571
|
C | G | 1 | a0001c0002t0002g0226 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.555+174C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774571 | ||||||
chrX:15774577
|
T | C | 1 | a0001c0001t0030g0257 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.555+180T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774577 | ||||||
chrX:15774650
|
A | G | 1 | a0001c0001t0003g0035 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.555+253A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774650 | ||||||
chrX:15774786
|
C | CAAGA | 1 | a0001c0001t0001g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.555+390_555+393dup others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 15774786 | |||||
chrX:15774806
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0154 | 2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.555+409C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774806 | ||||||
chrX:15774839
|
C | T | 1 | a0001c0002t0002g0246 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.556-407C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774839 | ||||||
chrX:15774855
|
T | A | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.556-391T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774855 | ||||||
chrX:15775365
|
C | T | 1 | a0001c0002t0002g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.618+57C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775365 | ||||||
chrX:15775440
|
C | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(8): Show | 13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.618+132C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775440 | ||||||
chrX:15775465
|
GTCA | G | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.618+162_618+164del others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 15775465 | |||||
chrX:15775480
|
G | C | 1 | a0001c0001t0009g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.618+172G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775480 | ||||||
chrX:15775626
|
G | T | 105 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0001t0012g0262others(102): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.618+318G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775626 | ||||||
chrX:15775651
|
C | A | 118 | a0001c0001t0005g0067a0001c0001t0005g0086a0001c0001t0008g0024others(115): Show | 123 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.618+343C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775651 | ||||||
chrX:15775807
|
C | T | 9 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0127others(6): Show | 9 | HG02145.hp1 HG02293.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+499C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775807 | ||||||
chrX:15775812
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.618+504A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775812 | ||||||
chrX:15775847
|
C | A | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.618+539C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775847 | ||||||
chrX:15775885
|
C | T | 1 | a0001c0002t0002g0208 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.618+577C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775885 | ||||||
chrX:15776066
|
C | T | 1 | a0001c0001t0015g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.619-648C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776066 | ||||||
chrX:15776067
|
A | G | 1 | a0001c0001t0015g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.619-647A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776067 | ||||||
chrX:15776155
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(106): Show | 113 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.619-559A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776155 | ||||||
chrX:15776193
|
G | T | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-521G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776193 | ||||||
chrX:15776263
|
C | T | 2 | a0001c0002t0002g0256a0001c0002t0028g0180 | 2 | HG00280.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.619-451C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776263 | ||||||
chrX:15776290
|
G | T | 1 | a0001c0001t0005g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.619-424G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776290 | ||||||
chrX:15776326
|
G | A | 3 | a0001c0001t0013g0249a0001c0001t0013g0258a0001c0001t0030g0257 | 3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.619-388G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776326 | ||||||
chrX:15776338
|
C | CA | 107 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0088others(104): Show | 112 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.619-357dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 15776338 | |||||
chrX:15776338
|
C | CAA | 7 | a0001c0002t0002g0171a0001c0002t0002g0178a0001c0002t0002g0193others(4): Show | 7 | HG01243.hp1 HG03688.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-358_619-357dup others(2): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 15776338 | |||||
chrX:15776338
|
CA | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0150 | 2 | HG01168.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.619-357delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 15776338 | |||||
chrX:15776404
|
G | A | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.619-310G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776404 | ||||||
chrX:15776545
|
T | C | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.619-169T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776545 | ||||||
chrX:15776614
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0073others(4): Show | 7 | HG00597.hp2 HG01168.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-100C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776614 | ||||||
chrX:15776641
|
G | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(165): Show | 172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.619-73G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776641 | ||||||
chrX:15776653
|
T | C | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-61T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776653 | ||||||
chrX:15776692
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.619-22G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776692 | ||||||
chrX:15776882
|
C | A | 1 | a0001c0001t0003g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.774+13C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15776882 | ||||||
chrX:15776975
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.774+106A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15776975 | ||||||
chrX:15777177
|
AG | A | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.774+311delG | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15777177 | |||||
chrX:15777358
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.774+489T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777358 | ||||||
chrX:15777431
|
A | T | 1 | a0001c0002t0002g0236 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.774+562A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777431 | ||||||
chrX:15777466
|
G | GA | 1 | a0001c0004t0001g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.774+604dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15777466 | |||||
chrX:15777541
|
C | G | 47 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(44): Show | 47 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.774+672C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777541 | ||||||
chrX:15777680
|
A | G | 1 | a0001c0001t0013g0258 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.774+811A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777680 | ||||||
chrX:15777817
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0125 | 2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.774+948T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777817 | ||||||
chrX:15777976
|
C | T | 1 | a0001c0001t0029g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.774+1107C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777976 | ||||||
chrX:15778078
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.774+1209A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778078 | ||||||
chrX:15778367
|
T | C | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+1498T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778367 | ||||||
chrX:15778396
|
C | A | 2 | a0001c0002t0002g0204a0001c0002t0002g0225 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.774+1527C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778396 | ||||||
chrX:15778632
|
G | A | 3 | a0001c0002t0002g0194a0001c0002t0002g0251a0001c0002t0004g0232 | 3 | HG02523.hp2 NA18969.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.774+1763G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778632 | ||||||
chrX:15778828
|
A | G | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.774+1959A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778828 | ||||||
chrX:15779304
|
C | A | 1 | a0001c0002t0002g0223 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.774+2435C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779304 | ||||||
chrX:15779346
|
A | T | 1 | a0001c0002t0007g0165 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.774+2477A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779346 | ||||||
chrX:15779631
|
G | T | 29 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(26): Show | 29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.774+2762G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779631 | ||||||
chrX:15779633
|
GA | G | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.774+2771delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15779633 | |||||
chrX:15779638
|
A | C | 1 | a0001c0001t0020g0097 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.774+2769A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779638 | ||||||
chrX:15779837
|
CT | C | 1 | a0001c0002t0002g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.775-2646delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15779837 | |||||
chrX:15779927
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.775-2558C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779927 | ||||||
chrX:15780081
|
C | T | 80 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(77): Show | 85 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.775-2404C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780081 | ||||||
chrX:15780104
|
A | G | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-2381A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780104 | ||||||
chrX:15780107
|
AT | A | 1 | a0001c0001t0001g0092 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.775-2374delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15780107 | |||||
chrX:15780134
|
A | G | 7 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0127others(4): Show | 7 | HG02145.hp1 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-2351A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780134 | ||||||
chrX:15780196
|
A | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.775-2289A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780196 | ||||||
chrX:15780276
|
C | CG | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-2209_775-2208i others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780276 | ||||||
chrX:15780277
|
A | T | 30 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-2208A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780277 | ||||||
chrX:15780277
|
AT | A | 108 | a0001c0001t0001g0082a0001c0001t0001g0116a0001c0001t0010g0025others(105): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.775-2193delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15780277 | |||||
chrX:15780277
|
ATT | A | 2 | a0001c0002t0002g0253a0001c0002t0025g0191 | 2 | NA18963.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.775-2194_775-2193d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15780277 | |||||
chrX:15780318
|
G | C | 3 | a0001c0001t0010g0025a0001c0001t0010g0026a0001c0001t0010g0027 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.775-2167G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780318 | ||||||
chrX:15780340
|
T | C | 1 | a0001c0002t0002g0234 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-2145T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780340 | ||||||
chrX:15780367
|
C | G | 41 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-2118C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780367 | ||||||
chrX:15780403
|
G | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02630.hp2 HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.775-2082G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780403 | ||||||
chrX:15780460
|
A | G | 41 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-2025A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780460 | ||||||
chrX:15780523
|
C | T | 6 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-1962C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780523 | ||||||
chrX:15780626
|
A | G | 2 | a0001c0002t0002g0204a0001c0002t0002g0225 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.775-1859A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780626 | ||||||
chrX:15780681
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.775-1804C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780681 | ||||||
chrX:15780776
|
G | A | 3 | a0001c0002t0002g0217a0001c0002t0002g0242a0001c0002t0004g0218 | 3 | HG02109.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.775-1709G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780776 | ||||||
chrX:15780976
|
G | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-1509G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780976 | ||||||
chrX:15780981
|
C | CT | 13 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.775-1490dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15780981 | |||||
chrX:15781028
|
G | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0140 | 2 | NA18952.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.775-1457G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781028 | ||||||
chrX:15781085
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.775-1400A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781085 | ||||||
chrX:15781104
|
A | C | 1 | a0001c0002t0007g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775-1381A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781104 | ||||||
chrX:15781123
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.775-1362A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781123 | ||||||
chrX:15781780
|
C | T | 1 | a0001c0002t0002g0171 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.775-705C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781780 | ||||||
chrX:15781865
|
G | C | 2 | a0001c0001t0015g0023a0001c0001t0016g0022 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.775-620G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781865 | ||||||
chrX:15781890
|
G | A | 1 | a0001c0001t0008g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.775-595G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781890 | ||||||
chrX:15781918
|
TA | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.775-559delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15781918 | |||||
chrX:15781925
|
AAC | A | 103 | a0001c0001t0012g0262a0001c0001t0012g0263a0001c0001t0013g0249others(100): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.775-558_775-557del others(2): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15781925 | |||||
chrX:15781926
|
A | C | 5 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0146others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-559A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781926 | ||||||
chrX:15781927
|
C | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0146others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-558C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781927 | ||||||
chrX:15781928
|
A | C | 103 | a0001c0001t0012g0262a0001c0001t0012g0263a0001c0001t0013g0249others(100): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.775-557A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781928 | ||||||
chrX:15781953
|
GA | G | 1 | a0001c0001t0006g0098 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.775-522delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15781953 | |||||
chrX:15782074
|
G | A | 1 | a0001c0001t0008g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.775-411G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782074 | ||||||
chrX:15782278
|
C | T | 1 | a0001c0002t0002g0190 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.775-207C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782278 | ||||||
chrX:15782282
|
A | G | 41 | a0001c0001t0003g0004a0001c0001t0003g0011a0001c0001t0003g0012others(38): Show | 41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-203A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782282 | ||||||
chrX:15782475
|
C | G | 1 | a0001c0001t0031g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.775-10C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782475 | ||||||
chrX:15782477
|
A | G | 96 | a0001c0002t0002g0001a0001c0002t0002g0007a0001c0002t0002g0008others(93): Show | 101 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
splice_region_variant&intron_variant | LOW | c.775-8A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782477 |