Item | Value |
---|---|
geneid | 3597 |
ensemblid | ENSG00000131724.11 |
hgncid | 5974 |
symbol | IL13RA1 |
name | interleukin 13 receptor subunit alpha 1 |
refseq_nuc | NM_001560.3 |
refseq_prot | NP_001551.1 |
ensembl_nuc | ENST00000371666.8 |
ensembl_prot | ENSP00000360730.3 |
mane_status | MANE Select |
chr | chrX |
start | 118727606 |
end | 118794533 |
strand | + |
ver | v1.2 |
region | chrX:118727606-118794533 |
region5000 | chrX:118722606-118799533 |
regionname0 | IL13RA1_chrX_118727606_118794533 |
regionname5000 | IL13RA1_chrX_118722606_118799533 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 427 | 272 | 68 | 49 | 120 | 10 | 23 | 93 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0002 | 0/0 | 42 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0003 | 0/0 | 427 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0004 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0005 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0006 | 0/0 | 427 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0007 | 0/0 | 42 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1284 | 262 | 67 | 48 | 113 | 9 | 23 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0002 | 0/0 | 1284 | 9 | 1 | 0 | 7 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0003 | 0/0 | 1285 | 3 | 0 | 0 | 3 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0004 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0005 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0006 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0007 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0008 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
c0009 | 0/0 | 1285 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2713 | 173 | 63 | 27 | 60 | 8 | 13 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0002 | 0/0 | 2716 | 84 | 2 | 20 | 53 | 2 | 7 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0003 | 0/0 | 2713 | 4 | 0 | 0 | 2 | 0 | 2 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0004 | 0/0 | 2713 | 2 | 0 | 0 | 2 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0005 | 0/0 | 2718 | 2 | 1 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0006 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0007 | 0/0 | 2713 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0008 | 0/0 | 2713 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0009 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0010 | 0/0 | 2713 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0011 | 0/0 | 2714 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0012 | 0/0 | 2710 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0013 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0014 | 0/0 | 2713 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0015 | 0/0 | 2716 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0016 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0017 | 0/0 | 2716 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0018 | 0/0 | 2716 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0019 | 0/0 | 2716 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
t0020 | 0/0 | 2716 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1284 | 262 | 67 | 48 | 113 | 9 | 23 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0001c0002 | 0/0 | 1284 | 9 | 1 | 0 | 7 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0001c0008 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0002c0003 | 0/0 | 1285 | 3 | 0 | 0 | 3 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0003c0006 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0004c0004 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0005c0005 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0006c0007 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 | |
a0007c0009 | 0/0 | 1285 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3996 | 159 | 60 | 27 | 51 | 6 | 13 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0002 | 0/0 | 3999 | 82 | 2 | 20 | 52 | 2 | 6 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0003 | 0/0 | 3996 | 4 | 0 | 0 | 2 | 0 | 2 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0004 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0005 | 0/0 | 4001 | 2 | 1 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0006 | 0/0 | 3994 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0007 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0008 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0009 | 0/0 | 3995 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0010 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0011 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0012 | 0/0 | 3993 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0013 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0014 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0016 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0017 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0018 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0001t0019 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0002t0001 | 0/0 | 3996 | 9 | 1 | 0 | 7 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0001c0008t0020 | 0/0 | 3999 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0002c0003t0001 | 0/0 | 3997 | 2 | 0 | 0 | 2 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0002c0003t0015 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0003c0006t0001 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0004c0004t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0005c0005t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0006c0007t0002 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
a0007c0009t0002 | 0/0 | 4000 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | copy fasta | chrX | 118722606 | 118799533 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0009g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0010g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0011g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0013g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0014g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0016g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0018g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0001t0019g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0001c0008t0020g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0002c0003t0015g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0003c0006t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0004c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0005c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0006c0007t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
a0007c0009t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0119 | EUR | GBR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | FIN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | FIN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01081 | hp1 | a0001 | c0008 | t0020 | g0031 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | IBS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0255 | EUR | IBS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01993 | hp1 | a0001 | c0001 | t0010 | g0151 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02056 | hp1 | a0001 | c0001 | t0017 | g0085 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CDX | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CDX | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CDX | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02647 | hp1 | a0004 | c0004 | t0001 | g0134 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0258 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0059 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | STU | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | BEB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03942 | hp1 | a0001 | c0001 | t0019 | g0069 | SAS | BEB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | STU | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG04204 | hp1 | a0006 | c0007 | t0002 | g0030 | SAS | STU | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18948 | hp1 | a0001 | c0001 | t0011 | g0185 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18954 | hp2 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18974 | hp2 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18983 | hp1 | a0001 | c0001 | t0018 | g0094 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0251 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19072 | hp1 | a0001 | c0001 | t0009 | g0167 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19076 | hp1 | a0007 | c0009 | t0002 | g0264 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19078 | hp1 | a0002 | c0003 | t0015 | g0091 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0234 | AFR | YRI | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA20129 | hp1 | a0001 | c0001 | t0014 | g0137 | AFR | ASW | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ASW | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA20752 | hp1 | a0003 | c0006 | t0001 | g0222 | EUR | TSI | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02559 | hp1 | a0005 | c0005 | t0001 | g0230 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | ACB | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | USA | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | USA | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | USA | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | USA | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0252 | AFR | LWK | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0144 | REF | REF | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0110 | REF | REF | IL13RA1_chrX_118722606_118799533 | IL13RA1 | chrX | 118722606 | 118799533 |
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:118727695 | C | CG | 1 | a0002 | 3 | NA18974.hp2 NA19001.hp1 NA19078.hp1 |
frameshift_variant | HIGH | c.62dupG | p.Gly22fs | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/11 | 96/3996 | 63/1284 | 21/427 | INFO_REALIGN_3_PRIME | chrX | 118727695 | |
chrX:118727707 | C | CG | 1 | a0007 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.74dupG | p.Ala26fs | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/11 | 108/3996 | 75/1284 | 25/427 | INFO_REALIGN_3_PRIME | chrX | 118727707 | |
chrX:118766555 | C | G | 1 | a0006 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.854C>G | p.Pro285Arg | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 7/11 | 887/3996 | 854/1284 | 285/427 | chrX | 118766555 | ||
chrX:118766924 | A | C | 1 | a0003 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.957A>C | p.Leu319Phe | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/11 | 990/3996 | 957/1284 | 319/427 | chrX | 118766924 | ||
chrX:118791762 | C | T | 1 | a0005 | 1 | HG02559.hp1 | missense_variant&splice_region_variant | MODERATE | c.1192C>T | p.His398Tyr | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1225/3996 | 1192/1284 | 398/427 | chrX | 118791762 | ||
chrX:118791810 | G | A | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1240G>A | p.Asp414Asn | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1273/3996 | 1240/1284 | 414/427 | chrX | 118791810 |
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:118761259 | C | T | 1 | a0001c0008 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.798C>T | p.Asn266Asn | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/11 | 831/3996 | 798/1284 | 266/427 | chrX | 118761259 | ||
chrX:118773919 | C | T | 1 | a0001c0002 | 9 | HG00099.hp1 HG02027.hp1 HG02083.hp1 others(6): Show |
synonymous_variant | LOW | c.1050C>T | p.Leu350Leu | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/11 | 1083/3996 | 1050/1284 | 350/427 | chrX | 118773919 |
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:118791912 | ATT | A | 1 | a0001c0001t0006 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60_*61delTT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 60 | INFO_REALIGN_3_PRIME | chrX | 118791912 | ||||
chrX:118791935 | A | G | 9 | a0001c0001t0002a0001c0001t0016a0001c0001t0017others(6): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*81A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 81 | chrX | 118791935 | |||||
chrX:118791991 | G | A | 1 | a0001c0001t0007 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 137 | chrX | 118791991 | |||||
chrX:118792013 | C | T | 1 | a0001c0001t0014 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 159 | chrX | 118792013 | |||||
chrX:118792035 | G | A | 1 | a0001c0001t0004 | 2 | NA18980.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*181G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 181 | chrX | 118792035 | |||||
chrX:118792143 | A | G | 1 | a0001c0001t0003 | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*289A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 289 | chrX | 118792143 | |||||
chrX:118792403 | TG | T | 1 | a0002c0003t0015 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 552 | INFO_REALIGN_3_PRIME | chrX | 118792403 | ||||
chrX:118792416 | C | T | 8 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(5): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*562C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 562 | chrX | 118792416 | |||||
chrX:118792515 | G | A | 1 | a0001c0001t0008 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*661G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 661 | chrX | 118792515 | |||||
chrX:118792529 | C | T | 1 | a0001c0008t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*675C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 675 | chrX | 118792529 | |||||
chrX:118792538 | C | CG | 1 | a0002c0003t0015 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*687dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 688 | INFO_REALIGN_3_PRIME | chrX | 118792538 | ||||
chrX:118792646 | A | AAAAAC | 2 | a0001c0001t0005a0001c0001t0013 | 3 | HG01517.hp1 HG02559.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*817_*821dupCAAAA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 822 | INFO_REALIGN_3_PRIME | chrX | 118792646 | ||||
chrX:118792650 | A | G | 1 | a0001c0001t0019 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*796A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 796 | chrX | 118792650 | |||||
chrX:118792676 | AAAC | A | 1 | a0001c0001t0012 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*823_*825delAAC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 823 | chrX | 118792676 | |||||
chrX:118792757 | C | CATG | 8 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(5): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*908_*910dupTGA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 911 | INFO_REALIGN_3_PRIME | chrX | 118792757 | ||||
chrX:118792818 | T | G | 8 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(5): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*964T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 964 | chrX | 118792818 | |||||
chrX:118793020 | CT | C | 1 | a0001c0001t0009 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1176delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1176 | INFO_REALIGN_3_PRIME | chrX | 118793020 | ||||
chrX:118793070 | A | G | 1 | a0001c0001t0003 | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1216A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1216 | chrX | 118793070 | |||||
chrX:118793379 | T | C | 1 | a0001c0001t0017 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1525T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1525 | chrX | 118793379 | |||||
chrX:118793396 | A | T | 1 | a0001c0001t0013 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1542A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1542 | chrX | 118793396 | |||||
chrX:118793478 | A | T | 1 | a0001c0001t0003 | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1624A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1624 | chrX | 118793478 | |||||
chrX:118793485 | T | TG | 1 | a0001c0001t0011 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 1638 | INFO_REALIGN_3_PRIME | chrX | 118793485 | ||||
chrX:118793939 | G | A | 1 | a0001c0001t0010 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2085G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 2085 | chrX | 118793939 | |||||
chrX:118794019 | TC | T | 1 | a0001c0001t0016 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2170delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 2170 | INFO_REALIGN_3_PRIME | chrX | 118794019 | ||||
chrX:118794049 | T | G | 1 | a0001c0001t0018 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2195T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 11/11 | 2195 | chrX | 118794049 |
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:118727748 | C | T | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+22C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118727748 | ||||||
chrX:118727859 | A | AG | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+135dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118727859 | |||||
chrX:118727935 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88+209C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118727935 | ||||||
chrX:118727977 | G | GT | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+251_88+252insT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118727977 | ||||||
chrX:118728054 | C | CG | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.88+334dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118728054 | |||||
chrX:118728128 | A | AC | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+402_88+403insC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728128 | ||||||
chrX:118728163 | C | A | 1 | a0001c0001t0002g0011 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.88+437C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728163 | ||||||
chrX:118728205 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+479C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728205 | ||||||
chrX:118728371 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.88+645C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728371 | ||||||
chrX:118728464 | TC | T | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+741delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118728464 | |||||
chrX:118728528 | T | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0013 | 2 | NA18939.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.88+802T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728528 | ||||||
chrX:118728625 | C | CA | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+900dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118728625 | |||||
chrX:118728653 | T | A | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+927T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728653 | ||||||
chrX:118728658 | C | G | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+932C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728658 | ||||||
chrX:118728768 | G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 7 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+1042G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728768 | ||||||
chrX:118728812 | C | CG | 1 | a0001c0001t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.88+1092dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118728812 | |||||
chrX:118728949 | A | G | 2 | a0001c0001t0002g0093a0001c0001t0018g0094 | 2 | HG02293.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.88+1223A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118728949 | ||||||
chrX:118729141 | GA | G | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+1417delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118729141 | |||||
chrX:118729149 | G | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0015others(1): Show | 4 | HG00423.hp1 NA18966.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1423G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118729149 | ||||||
chrX:118729170 | G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0263 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.88+1444G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118729170 | ||||||
chrX:118729348 | TC | T | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+1626delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118729348 | |||||
chrX:118729422 | GT | G | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.88+1700delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118729422 | |||||
chrX:118729526 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.88+1800C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118729526 | ||||||
chrX:118729691 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.88+1965G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118729691 | ||||||
chrX:118729785 | A | G | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+2059A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118729785 | ||||||
chrX:118729942 | C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+2216C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118729942 | ||||||
chrX:118730026 | C | T | 86 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.88+2300C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118730026 | ||||||
chrX:118730162 | G | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.88+2436G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118730162 | ||||||
chrX:118730801 | A | G | 2 | a0001c0001t0001g0254a0001c0001t0005g0255 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.88+3075A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118730801 | ||||||
chrX:118731007 | GC | G | 1 | a0001c0001t0002g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.88+3282delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731007 | ||||||
chrX:118731153 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.88+3427C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731153 | ||||||
chrX:118731258 | G | A | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG00621.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.88+3532G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731258 | ||||||
chrX:118731476 | C | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA19058.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.88+3750C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731476 | ||||||
chrX:118731515 | T | A | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+3789T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731515 | ||||||
chrX:118731526 | A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.88+3800A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731526 | ||||||
chrX:118731539 | C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+3813C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731539 | ||||||
chrX:118731540 | G | A | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+3814G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731540 | ||||||
chrX:118731577 | C | CA | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(6): Show | 9 | HG00099.hp1 HG00099.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+3868dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118731577 | |||||
chrX:118731577 | CA | C | 89 | a0001c0001t0001g0086a0001c0001t0001g0106a0001c0001t0002g0001others(86): Show | 92 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.88+3868delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118731577 | |||||
chrX:118731577 | CAA | C | 1 | a0001c0001t0002g0092 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.88+3867_88+3868del others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118731577 | |||||
chrX:118731690 | G | A | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+3964G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731690 | ||||||
chrX:118731930 | T | G | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+4204T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118731930 | ||||||
chrX:118732074 | A | C | 1 | a0001c0001t0012g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.88+4348A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732074 | ||||||
chrX:118732229 | C | T | 1 | a0002c0003t0001g0251 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.88+4503C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732229 | ||||||
chrX:118732312 | C | CT | 1 | a0002c0003t0001g0251 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.88+4592dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118732312 | |||||
chrX:118732398 | T | TTA | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02155.hp2 NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.88+4688_88+4689dup others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118732398 | |||||
chrX:118732398 | TTA | T | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+4688_88+4689del others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118732398 | |||||
chrX:118732425 | C | T | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+4699C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732425 | ||||||
chrX:118732441 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.88+4715C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732441 | ||||||
chrX:118732520 | A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA19058.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.88+4794A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732520 | ||||||
chrX:118732553 | A | AG | 1 | a0002c0003t0001g0251 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.88+4827_88+4828ins others(1): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732553 | ||||||
chrX:118732553 | A | AT | 1 | a0002c0003t0015g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.88+4828dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118732553 | |||||
chrX:118732554 | T | TC | 1 | a0001c0001t0001g0250 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.88+4834dupC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118732554 | |||||
chrX:118732593 | C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0089others(1): Show | 4 | HG00558.hp2 HG02155.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+4867C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732593 | ||||||
chrX:118732957 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.88+5231A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118732957 | ||||||
chrX:118732989 | T | TA | 1 | a0001c0001t0002g0021 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.88+5267dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118732989 | |||||
chrX:118733033 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.88+5307C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118733033 | ||||||
chrX:118733135 | G | GT | 1 | a0001c0001t0002g0021 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.88+5413dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118733135 | |||||
chrX:118733310 | G | GT | 1 | a0001c0001t0002g0021 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.88+5590dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118733310 | |||||
chrX:118733327 | A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0246a0001c0001t0001g0247others(11): Show | 15 | HG00558.hp1 HG00621.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+5601A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118733327 | ||||||
chrX:118733337 | G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.88+5611G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118733337 | ||||||
chrX:118733521 | T | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG03017.hp1 HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.88+5795T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118733521 | ||||||
chrX:118733752 | A | C | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+6026A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118733752 | ||||||
chrX:118733753 | G | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.88+6027G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118733753 | ||||||
chrX:118733785 | A | AT | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.88+6069dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118733785 | |||||
chrX:118733797 | C | CTTGGTA | 1 | a0001c0001t0001g0245 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.88+6076_88+6081dup others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118733797 | |||||
chrX:118733874 | A | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG02155.hp2 NA18965.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+6148A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118733874 | ||||||
chrX:118734070 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88+6344G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118734070 | ||||||
chrX:118734828 | G | A | 1 | a0001c0002t0001g0142 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-6189G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118734828 | ||||||
chrX:118734904 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.89-6113A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118734904 | ||||||
chrX:118734924 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.89-6093T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118734924 | ||||||
chrX:118735072 | G | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 6 | HG00558.hp1 HG01496.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-5945G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118735072 | ||||||
chrX:118735121 | T | TA | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.89-5895dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118735121 | |||||
chrX:118735759 | G | A | 1 | a0001c0001t0012g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.89-5258G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118735759 | ||||||
chrX:118735989 | CAAT | C | 1 | a0001c0001t0001g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.89-5024_89-5022del others(3): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118735989 | |||||
chrX:118736160 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.89-4857T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118736160 | ||||||
chrX:118736421 | C | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.89-4596C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118736421 | ||||||
chrX:118736571 | TTC | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG00609.hp1 NA18969.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-4444_89-4443del others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118736571 | |||||
chrX:118736638 | G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(17): Show | 22 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.89-4379G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118736638 | ||||||
chrX:118736653 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.89-4364C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118736653 | ||||||
chrX:118736770 | C | A | 87 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0002g0001others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.89-4247C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118736770 | ||||||
chrX:118736883 | C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0263 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.89-4134C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118736883 | ||||||
chrX:118737084 | A | G | 1 | a0001c0001t0001g0009 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.89-3933A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118737084 | ||||||
chrX:118737119 | G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(17): Show | 22 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.89-3898G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118737119 | ||||||
chrX:118737395 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.89-3622T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118737395 | ||||||
chrX:118737500 | T | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(27): Show | 33 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-3517T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118737500 | ||||||
chrX:118737599 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.89-3418C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118737599 | ||||||
chrX:118738124 | C | A | 84 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(81): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.89-2893C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118738124 | ||||||
chrX:118738236 | T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-2781T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118738236 | ||||||
chrX:118738253 | G | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.89-2764G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118738253 | ||||||
chrX:118738309 | C | G | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2708C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118738309 | ||||||
chrX:118738401 | GTC | G | 1 | a0001c0001t0001g0146 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-2614_89-2613del others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118738401 | |||||
chrX:118738571 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-2446C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118738571 | ||||||
chrX:118738781 | C | CT | 17 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.89-2212dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118738781 | |||||
chrX:118738781 | CT | C | 86 | a0001c0001t0001g0019a0001c0001t0001g0107a0001c0001t0001g0147others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.89-2212delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118738781 | |||||
chrX:118738781 | CTT | C | 5 | a0001c0001t0002g0012a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG03831.hp2 HG04184.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2213_89-2212del others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118738781 | |||||
chrX:118740054 | TC | T | 1 | a0001c0001t0001g0236 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.89-960delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118740054 | |||||
chrX:118740112 | T | C | 15 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0027others(12): Show | 16 | HG00408.hp2 HG01081.hp1 NA18941.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-905T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118740112 | ||||||
chrX:118740227 | G | A | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-790G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118740227 | ||||||
chrX:118740811 | CTAA | C | 1 | a0001c0001t0001g0235 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.89-203_89-201delAT others(1): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118740811 | |||||
chrX:118740935 | T | C | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.89-82T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 1/10 | chrX | 118740935 | ||||||
chrX:118741241 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.228+85C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741241 | ||||||
chrX:118741301 | G | A | 9 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(6): Show | 9 | HG00621.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.228+145G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741301 | ||||||
chrX:118741435 | T | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.228+279T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741435 | ||||||
chrX:118741449 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.228+293A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741449 | ||||||
chrX:118741649 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.228+493C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741649 | ||||||
chrX:118741830 | G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 7 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+674G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741830 | ||||||
chrX:118741947 | G | C | 1 | a0001c0001t0002g0042 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.228+791G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741947 | ||||||
chrX:118741969 | G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.228+813G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118741969 | ||||||
chrX:118742041 | C | T | 1 | a0001c0001t0017g0085 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.228+885C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118742041 | ||||||
chrX:118742194 | G | T | 1 | a0001c0001t0012g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.228+1038G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118742194 | ||||||
chrX:118742612 | T | C | 1 | a0001c0008t0020g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.228+1456T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118742612 | ||||||
chrX:118742834 | C | T | 2 | a0001c0001t0005g0233a0001c0001t0013g0234 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.228+1678C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118742834 | ||||||
chrX:118743169 | G | A | 1 | a0001c0001t0012g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.228+2013G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118743169 | ||||||
chrX:118743474 | G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.228+2318G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118743474 | ||||||
chrX:118743512 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.228+2356A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118743512 | ||||||
chrX:118743688 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.228+2532G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118743688 | ||||||
chrX:118743997 | T | C | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.228+2841T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118743997 | ||||||
chrX:118744028 | C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.228+2872C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118744028 | ||||||
chrX:118744129 | G | A | 86 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.229-2825G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118744129 | ||||||
chrX:118744291 | A | T | 86 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.229-2663A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118744291 | ||||||
chrX:118744381 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229-2573A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118744381 | ||||||
chrX:118744762 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.229-2192A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118744762 | ||||||
chrX:118744825 | A | G | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.229-2129A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118744825 | ||||||
chrX:118744887 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.229-2067T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118744887 | ||||||
chrX:118745044 | C | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.229-1910C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118745044 | ||||||
chrX:118745224 | A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(7): Show | 11 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.229-1730A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118745224 | ||||||
chrX:118745351 | A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 8 | HG00639.hp2 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-1603A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118745351 | ||||||
chrX:118745397 | GGATTTTG others(6): Show |
G | 86 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.229-1554_229-1542d others(15): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118745397 | |||||
chrX:118745640 | T | C | 6 | a0001c0001t0001g0116a0001c0001t0001g0147a0001c0001t0001g0158others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-1314T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118745640 | ||||||
chrX:118745779 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.229-1175T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118745779 | ||||||
chrX:118745823 | CTG | C | 9 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(6): Show | 9 | HG00621.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.229-1129_229-1128d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118745823 | |||||
chrX:118746134 | G | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 9 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.229-820G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118746134 | ||||||
chrX:118746135 | A | AT | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.229-809dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118746135 | |||||
chrX:118746135 | A | ATT | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-810_229-809dup others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118746135 | |||||
chrX:118746135 | AT | A | 1 | a0001c0001t0001g0231 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.229-809delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118746135 | |||||
chrX:118746542 | G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02717.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.229-412G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118746542 | ||||||
chrX:118746864 | A | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.229-90A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 2/10 | chrX | 118746864 | ||||||
chrX:118747188 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.367+96A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118747188 | ||||||
chrX:118747350 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.367+258C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118747350 | ||||||
chrX:118747353 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.367+261G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118747353 | ||||||
chrX:118747355 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.367+263G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118747355 | ||||||
chrX:118747356 | C | T | 1 | a0005c0005t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367+264C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118747356 | ||||||
chrX:118747365 | A | G | 3 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02717.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.367+273A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118747365 | ||||||
chrX:118747389 | A | AC | 1 | a0001c0001t0001g0164 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.367+301dupC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118747389 | |||||
chrX:118747906 | TG | T | 1 | a0001c0001t0001g0165 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.367+817delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118747906 | |||||
chrX:118748005 | T | TTG | 18 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0168others(15): Show | 19 | HG00673.hp1 HG01074.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.367+945_367+946dup others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748005 | T | TTGTG | 49 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(46): Show | 52 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.367+943_367+946dup others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748005 | T | TTGTGTG | 97 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(94): Show | 100 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.367+941_367+946dup others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748005 | T | TTGTGTGT others(1): Show |
12 | a0001c0001t0001g0154a0001c0001t0001g0164a0001c0001t0001g0224others(9): Show | 12 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.367+939_367+946dup others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748005 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.367+935_367+946dup others(12): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748005 | TTG | T | 2 | a0001c0001t0001g0114a0001c0001t0002g0022 | 2 | HG01884.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.367+945_367+946del others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748005 | TTGTG | T | 1 | a0001c0001t0004g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.367+943_367+946del others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748005 | TTGTGTG | T | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.367+941_367+946del others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748005 | |||||
chrX:118748046 | C | A | 10 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0044others(7): Show | 10 | HG01346.hp1 HG01358.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.367+954C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118748046 | ||||||
chrX:118748068 | C | CAT | 2 | a0001c0001t0001g0153a0001c0001t0011g0185 | 2 | NA18948.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.367+984_367+985dup others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748068 | |||||
chrX:118748302 | G | C | 86 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.367+1210G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118748302 | ||||||
chrX:118748361 | G | GA | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0095others(37): Show | 42 | HG00639.hp1 HG00639.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.368-1278dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748361 | |||||
chrX:118748361 | G | GAA | 2 | a0001c0001t0001g0101a0001c0001t0001g0138 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.368-1279_368-1278d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748361 | |||||
chrX:118748361 | G | GGA | 63 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(60): Show | 65 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.367+1269_367+1270i others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118748361 | ||||||
chrX:118748361 | G | GGAA | 23 | a0001c0001t0001g0019a0001c0001t0002g0002a0001c0001t0002g0014others(20): Show | 24 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.367+1269_367+1270i others(5): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118748361 | ||||||
chrX:118748361 | GA | G | 1 | a0001c0001t0001g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.368-1278delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118748361 | |||||
chrX:118748790 | C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.368-868C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118748790 | ||||||
chrX:118748798 | A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0040 | 2 | NA18970.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.368-860A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 3/10 | chrX | 118748798 | ||||||
chrX:118749850 | C | CA | 1 | a0001c0001t0002g0040 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.488+82dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118749850 | |||||
chrX:118749891 | A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.488+113A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118749891 | ||||||
chrX:118750389 | T | TA | 2 | a0001c0001t0009g0167a0002c0003t0015g0091 | 2 | NA19072.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.488+623dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118750389 | |||||
chrX:118750389 | TA | T | 2 | a0001c0001t0001g0236a0001c0001t0002g0039 | 2 | NA19003.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.488+623delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118750389 | |||||
chrX:118750407 | C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.488+629C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118750407 | ||||||
chrX:118750726 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.488+948A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118750726 | ||||||
chrX:118750742 | C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0095others(99): Show | 106 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.488+964C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118750742 | ||||||
chrX:118751355 | CA | C | 1 | a0001c0001t0001g0223 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.488+1583delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751355 | |||||
chrX:118751385 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.488+1607C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118751385 | ||||||
chrX:118751588 | TG | T | 1 | a0001c0001t0001g0223 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.488+1815delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751588 | |||||
chrX:118751777 | A | G | 1 | a0003c0006t0001g0222 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.488+1999A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118751777 | ||||||
chrX:118751884 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.488+2106A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118751884 | ||||||
chrX:118751896 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.488+2118A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118751896 | ||||||
chrX:118751900 | C | CA | 11 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0155others(8): Show | 11 | HG01243.hp1 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.488+2141dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751900 | |||||
chrX:118751900 | C | CAA | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(27): Show | 33 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.488+2140_488+2141d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751900 | |||||
chrX:118751900 | C | CAAA | 84 | a0001c0001t0001g0019a0001c0001t0001g0115a0001c0001t0001g0132others(81): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.488+2139_488+2141d others(5): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751900 | |||||
chrX:118751900 | C | CAAAA | 4 | a0001c0001t0002g0032a0001c0001t0002g0055a0001c0001t0002g0056others(1): Show | 4 | HG01934.hp1 HG02300.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+2138_488+2141d others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751900 | |||||
chrX:118751900 | CA | C | 8 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0148others(5): Show | 8 | HG02717.hp1 HG03195.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.488+2141delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751900 | |||||
chrX:118751900 | CAAAAAAA others(1): Show |
C | 1 | a0001c0001t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.488+2134_488+2141d others(10): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118751900 | |||||
chrX:118752073 | C | T | 261 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(258): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.488+2295C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118752073 | ||||||
chrX:118752320 | A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 8 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.488+2542A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118752320 | ||||||
chrX:118752402 | G | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 39 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.488+2624G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118752402 | ||||||
chrX:118752581 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.488+2803T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118752581 | ||||||
chrX:118752807 | T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0263 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.488+3029T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118752807 | ||||||
chrX:118752872 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.488+3094G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118752872 | ||||||
chrX:118752873 | G | T | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG00621.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.488+3095G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118752873 | ||||||
chrX:118753001 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.488+3223T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753001 | ||||||
chrX:118753045 | G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.488+3267G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753045 | ||||||
chrX:118753149 | ATCCCAGC others(3): Show |
A | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.488+3373_488+3382d others(12): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118753149 | |||||
chrX:118753392 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.488+3614A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753392 | ||||||
chrX:118753467 | G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.488+3689G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753467 | ||||||
chrX:118753631 | A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.488+3853A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753631 | ||||||
chrX:118753834 | T | C | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.488+4056T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753834 | ||||||
chrX:118753835 | A | T | 85 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(82): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.488+4057A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753835 | ||||||
chrX:118753911 | C | T | 4 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0075others(1): Show | 4 | HG00642.hp1 HG01192.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+4133C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753911 | ||||||
chrX:118753953 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.489-4102T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118753953 | ||||||
chrX:118754029 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.489-4026G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754029 | ||||||
chrX:118754047 | TC | T | 1 | a0001c0001t0001g0223 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.489-4006delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118754047 | |||||
chrX:118754344 | A | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.489-3711A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754344 | ||||||
chrX:118754455 | G | A | 8 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG00621.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-3600G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754455 | ||||||
chrX:118754530 | A | G | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.489-3525A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754530 | ||||||
chrX:118754569 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.489-3486G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754569 | ||||||
chrX:118754618 | CA | C | 2 | a0001c0001t0002g0053a0001c0001t0002g0092 | 2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.489-3436delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754618 | ||||||
chrX:118754636 | C | CA | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(101): Show | 109 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.489-3409dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118754636 | |||||
chrX:118754636 | CA | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.489-3409delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118754636 | |||||
chrX:118754675 | T | TC | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 39 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.489-3380_489-3379i others(3): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754675 | ||||||
chrX:118754691 | C | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0263 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.489-3364C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754691 | ||||||
chrX:118754937 | C | CT | 16 | a0001c0001t0001g0008a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 17 | HG00408.hp1 HG00423.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.489-3104dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118754937 | |||||
chrX:118754937 | CT | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.489-3104delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118754937 | |||||
chrX:118754948 | T | C | 85 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(82): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.489-3107T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754948 | ||||||
chrX:118754951 | T | C | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.489-3104T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754951 | ||||||
chrX:118754952 | C | CT | 4 | a0001c0001t0001g0212a0001c0001t0001g0223a0001c0001t0005g0255others(1): Show | 4 | HG01517.hp1 HG01517.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.489-3089dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118754952 | |||||
chrX:118754952 | C | T | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.489-3103C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754952 | ||||||
chrX:118754952 | CT | C | 5 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0235others(2): Show | 5 | NA18953.hp1 NA18968.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-3089delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118754952 | |||||
chrX:118754998 | G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(17): Show | 22 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.489-3057G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118754998 | ||||||
chrX:118755041 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489-3014C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755041 | ||||||
chrX:118755192 | A | AC | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.489-2860dupC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118755192 | |||||
chrX:118755219 | G | T | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.489-2836G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755219 | ||||||
chrX:118755287 | C | T | 2 | a0001c0001t0005g0233a0001c0001t0013g0234 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.489-2768C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755287 | ||||||
chrX:118755384 | A | AT | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(23): Show | 28 | HG00639.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.489-2657dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118755384 | |||||
chrX:118755384 | A | ATT | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489-2658_489-2657d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118755384 | |||||
chrX:118755384 | AT | A | 15 | a0001c0001t0001g0100a0001c0001t0002g0048a0001c0001t0002g0053others(12): Show | 15 | HG00544.hp1 HG02293.hp2 HG03540.hp1 others(12): Show |
intron_variant | MODIFIER | c.489-2657delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118755384 | |||||
chrX:118755626 | T | C | 85 | a0001c0001t0001g0019a0001c0001t0002g0001a0001c0001t0002g0002others(82): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.489-2429T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755626 | ||||||
chrX:118755646 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.489-2409G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755646 | ||||||
chrX:118755685 | A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 5 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-2370A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755685 | ||||||
chrX:118755704 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.489-2351C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755704 | ||||||
chrX:118755816 | A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0074 | 2 | HG01952.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.489-2239A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755816 | ||||||
chrX:118755846 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.489-2209C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755846 | ||||||
chrX:118755927 | T | TG | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.489-2128_489-2127i others(3): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118755927 | ||||||
chrX:118756009 | G | GT | 1 | a0001c0008t0020g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.489-2033dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118756009 | |||||
chrX:118756009 | GT | G | 2 | a0001c0001t0001g0109a0001c0001t0002g0043 | 2 | HG01168.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.489-2033delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118756009 | |||||
chrX:118756493 | G | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 135 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.489-1562G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118756493 | ||||||
chrX:118756592 | A | G | 5 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-1463A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118756592 | ||||||
chrX:118757004 | G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(17): Show | 22 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.489-1051G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118757004 | ||||||
chrX:118757314 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.489-741T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118757314 | ||||||
chrX:118757524 | C | CA | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 72 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.489-511dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757524 | |||||
chrX:118757524 | C | CAA | 60 | a0001c0001t0001g0019a0001c0001t0001g0115a0001c0001t0001g0135others(57): Show | 62 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.489-512_489-511dup others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757524 | |||||
chrX:118757524 | C | CAAA | 30 | a0001c0001t0001g0131a0001c0001t0002g0015a0001c0001t0002g0017others(27): Show | 30 | HG00735.hp2 HG01081.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.489-513_489-511dup others(3): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757524 | |||||
chrX:118757524 | CA | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0209 | 2 | HG02155.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.489-511delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757524 | |||||
chrX:118757607 | T | TA | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.489-441dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757607 | |||||
chrX:118757678 | C | CT | 131 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(128): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.489-347dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | C | CTT | 28 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0113others(25): Show | 28 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.489-348_489-347dup others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | C | CTTT | 5 | a0001c0001t0001g0010a0001c0001t0001g0208a0001c0001t0001g0224others(2): Show | 6 | HG00558.hp1 HG01081.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.489-349_489-347dup others(3): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | C | CTTTT | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01928.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.489-350_489-347dup others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | C | CTTTTTT | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.489-352_489-347dup others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CT | C | 5 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0056others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.489-347delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CTTTTTT | C | 9 | a0001c0001t0001g0101a0001c0001t0001g0115a0001c0001t0001g0130others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.489-352_489-347del others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CTTTTTTT | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0127others(6): Show | 11 | HG00639.hp2 HG01884.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-353_489-347del others(7): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CTTTTTTT others(1): Show |
C | 1 | a0001c0001t0001g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.489-354_489-347del others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CTTTTTTT others(2): Show |
C | 3 | a0001c0001t0001g0097a0001c0001t0001g0266a0001c0001t0016g0252 | 3 | HG02257.hp1 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.489-355_489-347del others(9): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0001g0096a0001c0001t0001g0256a0001c0001t0001g0257others(7): Show | 10 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-356_489-347del others(10): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0098others(1): Show | 5 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-357_489-347del others(11): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757678 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-360_489-347del others(14): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118757678 | |||||
chrX:118757933 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.489-122C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 4/10 | chrX | 118757933 | ||||||
chrX:118758268 | A | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+26A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118758268 | ||||||
chrX:118758290 | T | C | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+48T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118758290 | ||||||
chrX:118758328 | C | G | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.676+86C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118758328 | ||||||
chrX:118758774 | G | T | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.676+532G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118758774 | ||||||
chrX:118759464 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.676+1222G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118759464 | ||||||
chrX:118759527 | G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0236 | 2 | NA18962.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.676+1285G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118759527 | ||||||
chrX:118759603 | C | T | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.676+1361C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118759603 | ||||||
chrX:118759929 | C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0126others(5): Show | 9 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.677-1209C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118759929 | ||||||
chrX:118760238 | TTC | T | 1 | a0002c0003t0001g0122 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.677-898_677-897del others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118760238 | |||||
chrX:118760376 | A | T | 12 | a0001c0001t0001g0161a0001c0001t0001g0168a0001c0001t0001g0171others(9): Show | 12 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.677-762A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118760376 | ||||||
chrX:118760416 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.677-722G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118760416 | ||||||
chrX:118760655 | T | C | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG00621.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.677-483T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118760655 | ||||||
chrX:118760958 | TA | T | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.677-177delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118760958 | |||||
chrX:118760995 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.677-143G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | chrX | 118760995 | ||||||
chrX:118761007 | TA | T | 1 | a0007c0009t0002g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.677-125delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118761007 | |||||
chrX:118761462 | A | T | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG00621.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.828+173A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118761462 | ||||||
chrX:118761691 | G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0128others(2): Show | 6 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.828+402G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118761691 | ||||||
chrX:118761721 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.828+432T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118761721 | ||||||
chrX:118762001 | A | G | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.828+712A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118762001 | ||||||
chrX:118762215 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.828+926T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118762215 | ||||||
chrX:118762556 | G | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG03017.hp1 HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.828+1267G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118762556 | ||||||
chrX:118762762 | GA | G | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+1476delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118762762 | |||||
chrX:118762786 | T | TTTAC | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+1499_828+1502d others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118762786 | |||||
chrX:118762841 | G | A | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.828+1552G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118762841 | ||||||
chrX:118763023 | G | A | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.828+1734G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118763023 | ||||||
chrX:118763075 | TG | T | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+1788delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763075 | |||||
chrX:118763118 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.828+1829A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118763118 | ||||||
chrX:118763196 | TA | T | 1 | a0001c0001t0002g0066 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.828+1914delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763196 | |||||
chrX:118763204 | G | GA | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+1919dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763204 | |||||
chrX:118763332 | A | AT | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+2045dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763332 | |||||
chrX:118763385 | G | GT | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+2097dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763385 | |||||
chrX:118763462 | C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0249 | 2 | HG01928.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.828+2173C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118763462 | ||||||
chrX:118763567 | C | CA | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+2281dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763567 | |||||
chrX:118763650 | GA | G | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+2367delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763650 | |||||
chrX:118763764 | C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0162 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.828+2475C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118763764 | ||||||
chrX:118763822 | C | CT | 86 | a0001c0001t0001g0019a0001c0001t0001g0098a0001c0001t0002g0001others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.828+2546dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763822 | |||||
chrX:118763822 | C | CTT | 12 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 13 | HG01099.hp1 HG01167.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.828+2545_828+2546d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763822 | |||||
chrX:118763822 | C | CTTT | 2 | a0001c0001t0001g0256a0001c0001t0001g0259 | 2 | HG01106.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.828+2544_828+2546d others(5): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763822 | |||||
chrX:118763822 | C | CTTTT | 1 | a0001c0001t0001g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.828+2543_828+2546d others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763822 | |||||
chrX:118763822 | CT | C | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+2546delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763822 | |||||
chrX:118763907 | TG | T | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828+2620delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118763907 | |||||
chrX:118764020 | C | CT | 3 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0210 | 4 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-2501dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764020 | |||||
chrX:118764020 | CT | C | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-2501delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764020 | |||||
chrX:118764180 | A | AC | 2 | a0001c0001t0002g0050a0001c0001t0009g0167 | 2 | HG02738.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.829-2344dupC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764180 | |||||
chrX:118764270 | AG | A | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-2255delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764270 | |||||
chrX:118764368 | AG | A | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-2159delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764368 | |||||
chrX:118764376 | CA | C | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-2152delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764376 | |||||
chrX:118764390 | A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 8 | HG00639.hp2 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-2140A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118764390 | ||||||
chrX:118764440 | T | TA | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-2087dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764440 | |||||
chrX:118764480 | G | GT | 3 | a0001c0001t0001g0226a0001c0001t0003g0102a0001c0001t0009g0167 | 3 | HG03688.hp1 NA18973.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.829-2040dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764480 | |||||
chrX:118764493 | CA | C | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-2035delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764493 | |||||
chrX:118764539 | TG | T | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-1989delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764539 | |||||
chrX:118764590 | T | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.829-1940T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118764590 | ||||||
chrX:118764598 | CA | C | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-1927delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764598 | |||||
chrX:118764614 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.829-1916G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118764614 | ||||||
chrX:118764621 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.829-1909G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118764621 | ||||||
chrX:118764722 | A | AG | 1 | a0001c0001t0009g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.829-1806dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764722 | |||||
chrX:118764830 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.829-1700T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118764830 | ||||||
chrX:118764869 | CT | C | 1 | a0001c0001t0001g0226 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.829-1656delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118764869 | |||||
chrX:118765001 | G | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.829-1529G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765001 | ||||||
chrX:118765096 | G | A | 1 | a0001c0001t0012g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.829-1434G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765096 | ||||||
chrX:118765110 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.829-1420C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765110 | ||||||
chrX:118765159 | G | A | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG00621.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.829-1371G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765159 | ||||||
chrX:118765162 | A | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.829-1368A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765162 | ||||||
chrX:118765217 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.829-1313C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765217 | ||||||
chrX:118765246 | T | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.829-1284T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765246 | ||||||
chrX:118765261 | C | CT | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0095others(26): Show | 31 | HG00639.hp2 HG01884.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.829-1254dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118765261 | |||||
chrX:118765261 | C | CTT | 14 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0156others(11): Show | 14 | HG00621.hp1 HG01243.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.829-1255_829-1254d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118765261 | |||||
chrX:118765261 | C | CTTT | 1 | a0001c0001t0001g0210 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.829-1256_829-1254d others(5): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118765261 | |||||
chrX:118765261 | CT | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 7 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.829-1254delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118765261 | |||||
chrX:118765475 | A | G | 10 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0044others(7): Show | 10 | HG01346.hp1 HG01358.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.829-1055A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765475 | ||||||
chrX:118765647 | C | T | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG00621.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.829-883C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765647 | ||||||
chrX:118765673 | A | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.829-857A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765673 | ||||||
chrX:118765915 | T | C | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.829-615T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765915 | ||||||
chrX:118765958 | A | T | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.829-572A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765958 | ||||||
chrX:118765988 | G | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.829-542G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118765988 | ||||||
chrX:118766303 | T | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.829-227T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118766303 | ||||||
chrX:118766320 | T | G | 1 | a0001c0001t0002g0028 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.829-210T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | chrX | 118766320 | ||||||
chrX:118766340 | C | CT | 3 | a0001c0001t0001g0205a0001c0001t0002g0047a0001c0001t0002g0053 | 3 | HG02735.hp1 NA18961.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.829-179dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 118766340 | |||||
chrX:118767048 | C | G | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1009+72C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767048 | ||||||
chrX:118767495 | T | G | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009+519T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767495 | ||||||
chrX:118767519 | C | T | 2 | a0001c0001t0002g0071a0001c0001t0002g0072 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1009+543C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767519 | ||||||
chrX:118767534 | G | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1009+558G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767534 | ||||||
chrX:118767692 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1009+716G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767692 | ||||||
chrX:118767695 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1009+719G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767695 | ||||||
chrX:118767838 | G | A | 2 | a0001c0001t0005g0233a0001c0001t0013g0234 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1009+862G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767838 | ||||||
chrX:118767885 | C | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0095others(19): Show | 24 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1009+909C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118767885 | ||||||
chrX:118768042 | A | G | 1 | a0001c0001t0001g0009 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1009+1066A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118768042 | ||||||
chrX:118768386 | A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1009+1410A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118768386 | ||||||
chrX:118768552 | C | T | 1 | a0001c0001t0008g0204 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1009+1576C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118768552 | ||||||
chrX:118768641 | G | C | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1009+1665G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118768641 | ||||||
chrX:118768678 | CCACACAG others(3): Show |
C | 16 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1009+1711_1009+172 others(14): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118768678 | |||||
chrX:118768913 | A | G | 9 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG00621.hp1 HG01243.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1009+1937A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118768913 | ||||||
chrX:118768940 | TC | T | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1009+1967delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118768940 | |||||
chrX:118769046 | G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1009+2070G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769046 | ||||||
chrX:118769152 | A | C | 1 | a0001c0001t0001g0236 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1009+2176A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769152 | ||||||
chrX:118769175 | A | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 6 | HG00558.hp1 HG01496.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1009+2199A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769175 | ||||||
chrX:118769264 | T | C | 3 | a0001c0001t0001g0212a0001c0001t0001g0254a0001c0001t0005g0255 | 3 | HG01515.hp1 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1009+2288T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769264 | ||||||
chrX:118769276 | TG | T | 1 | a0001c0002t0001g0150 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1009+2303delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118769276 | |||||
chrX:118769279 | G | GA | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1009+2308dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118769279 | |||||
chrX:118769547 | A | G | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(80): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1009+2571A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769547 | ||||||
chrX:118769560 | G | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009+2584G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769560 | ||||||
chrX:118769680 | C | T | 4 | a0001c0001t0003g0062a0001c0001t0003g0102a0001c0001t0003g0103others(1): Show | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009+2704C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769680 | ||||||
chrX:118769758 | C | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(80): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1009+2782C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769758 | ||||||
chrX:118769770 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1009+2794C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769770 | ||||||
chrX:118769868 | G | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0016 | 2 | NA18966.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1009+2892G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118769868 | ||||||
chrX:118770031 | TG | T | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1009+3057delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118770031 | |||||
chrX:118770110 | T | C | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 129 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1009+3134T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770110 | ||||||
chrX:118770126 | G | A | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009+3150G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770126 | ||||||
chrX:118770142 | A | AC | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1009+3168dupC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118770142 | |||||
chrX:118770158 | G | A | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1009+3182G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770158 | ||||||
chrX:118770172 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1009+3196C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770172 | ||||||
chrX:118770212 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1009+3236C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770212 | ||||||
chrX:118770222 | A | G | 87 | a0001c0001t0001g0141a0001c0001t0002g0001a0001c0001t0002g0002others(84): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1009+3246A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770222 | ||||||
chrX:118770265 | A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0232 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1009+3289A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770265 | ||||||
chrX:118770266 | T | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1009+3290T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770266 | ||||||
chrX:118770346 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1009+3370G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770346 | ||||||
chrX:118770451 | AC | A | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1010-3424delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118770451 | |||||
chrX:118770470 | T | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1010-3409T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770470 | ||||||
chrX:118770545 | C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 5 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-3334C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770545 | ||||||
chrX:118770559 | G | GC | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1010-3317dupC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118770559 | |||||
chrX:118770563 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1010-3316A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770563 | ||||||
chrX:118770685 | C | T | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1010-3194C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770685 | ||||||
chrX:118770686 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1010-3193G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770686 | ||||||
chrX:118770773 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1010-3106C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770773 | ||||||
chrX:118770852 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1010-3027G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118770852 | ||||||
chrX:118771049 | G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1010-2830G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771049 | ||||||
chrX:118771113 | T | G | 3 | a0001c0001t0001g0212a0001c0001t0001g0254a0001c0001t0005g0255 | 3 | HG01515.hp1 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1010-2766T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771113 | ||||||
chrX:118771223 | A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0263 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1010-2656A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771223 | ||||||
chrX:118771339 | C | T | 1 | a0001c0002t0001g0203 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1010-2540C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771339 | ||||||
chrX:118771364 | A | AG | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1010-2511dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118771364 | |||||
chrX:118771441 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1010-2438T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771441 | ||||||
chrX:118771456 | C | G | 2 | a0001c0001t0003g0062a0001c0001t0003g0104 | 2 | HG00621.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1010-2423C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771456 | ||||||
chrX:118771838 | G | A | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1010-2041G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771838 | ||||||
chrX:118771847 | G | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1010-2032G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118771847 | ||||||
chrX:118772274 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1010-1605C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118772274 | ||||||
chrX:118772276 | T | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1010-1603T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118772276 | ||||||
chrX:118772279 | G | A | 2 | a0001c0001t0002g0044a0001c0001t0016g0252 | 2 | NA18977.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1010-1600G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118772279 | ||||||
chrX:118772326 | G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0024 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1010-1553G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118772326 | ||||||
chrX:118772339 | T | A | 6 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0001t0003g0062others(3): Show | 6 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1010-1540T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118772339 | ||||||
chrX:118772596 | T | TA | 2 | a0001c0001t0001g0223a0001c0001t0002g0011 | 2 | NA19078.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1010-1274dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118772596 | |||||
chrX:118772822 | TGTTA | T | 1 | a0001c0001t0001g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1010-1053_1010-105 others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118772822 | |||||
chrX:118773319 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1010-560C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118773319 | ||||||
chrX:118773380 | A | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1010-499A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118773380 | ||||||
chrX:118773594 | T | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1010-285T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118773594 | ||||||
chrX:118773701 | CT | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 133 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1010-167delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 118773701 | |||||
chrX:118773835 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1010-44G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 8/10 | chrX | 118773835 | ||||||
chrX:118774058 | T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(11): Show | 15 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1106+83T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | chrX | 118774058 | ||||||
chrX:118774132 | C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(11): Show | 15 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1106+157C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | chrX | 118774132 | ||||||
chrX:118774152 | C | CT | 6 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 7 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1106+193dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 118774152 | |||||
chrX:118774152 | CT | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0263a0001c0001t0016g0252 | 3 | HG02809.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1106+193delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 118774152 | |||||
chrX:118774168 | T | TC | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1106+195dupC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 118774168 | |||||
chrX:118774203 | G | A | 4 | a0001c0001t0003g0062a0001c0001t0003g0102a0001c0001t0003g0103others(1): Show | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1106+228G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | chrX | 118774203 | ||||||
chrX:118774311 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1106+336G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | chrX | 118774311 | ||||||
chrX:118774349 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1106+374A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | chrX | 118774349 | ||||||
chrX:118774877 | T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0263 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1106+902T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | chrX | 118774877 | ||||||
chrX:118774886 | ACTCT | A | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1106+916_1106+919d others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 118774886 | |||||
chrX:118775332 | C | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1107-1095C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | chrX | 118775332 | ||||||
chrX:118776191 | A | AT | 1 | a0001c0001t0002g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1107-234dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 118776191 | |||||
chrX:118776517 | A | G | 5 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0175others(2): Show | 5 | HG03041.hp2 HG06807.hp1 NA18522.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1191+6A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118776517 | ||||||
chrX:118776541 | G | GT | 195 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(192): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1191+51dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776541 | |||||
chrX:118776541 | G | GTT | 32 | a0001c0001t0001g0019a0001c0001t0001g0146a0001c0001t0001g0148others(29): Show | 32 | HG02071.hp1 HG02145.hp1 HG02165.hp2 others(29): Show |
intron_variant | MODIFIER | c.1191+50_1191+51dup others(2): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776541 | |||||
chrX:118776541 | G | GTTT | 6 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0003g0104others(3): Show | 6 | HG00621.hp1 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1191+49_1191+51dup others(3): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776541 | |||||
chrX:118776541 | G | GTTTT | 1 | a0001c0001t0001g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1191+48_1191+51dup others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776541 | |||||
chrX:118776541 | GTTTTTTT | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 5 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+45_1191+51del others(7): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776541 | |||||
chrX:118776541 | GTTTTTTT others(3): Show |
G | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0095others(19): Show | 24 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1191+42_1191+51del others(10): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776541 | |||||
chrX:118776558 | T | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0095others(19): Show | 24 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1191+47T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118776558 | ||||||
chrX:118776582 | A | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+71A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118776582 | ||||||
chrX:118776588 | G | A | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1191+77G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118776588 | ||||||
chrX:118776702 | C | T | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1191+191C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118776702 | ||||||
chrX:118776951 | G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+440G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118776951 | ||||||
chrX:118776973 | ATATATGT others(3): Show |
A | 1 | a0001c0001t0013g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1191+474_1191+483d others(12): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776973 | |||||
chrX:118776997 | GTA | G | 35 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(32): Show | 35 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1191+509_1191+510d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776997 | |||||
chrX:118776997 | GTATA | G | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1191+507_1191+510d others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776997 | |||||
chrX:118776997 | GTATATA | G | 3 | a0001c0001t0001g0148a0001c0001t0001g0186a0005c0005t0001g0230 | 3 | HG02135.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1191+505_1191+510d others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118776997 | |||||
chrX:118777020 | T | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0002g0022others(2): Show | 5 | HG01884.hp2 HG03017.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+509T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118777020 | ||||||
chrX:118777030 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1191+519C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118777030 | ||||||
chrX:118777052 | T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1191+541T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118777052 | ||||||
chrX:118777757 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1191+1246C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118777757 | ||||||
chrX:118778242 | T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0126others(5): Show | 9 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1191+1731T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118778242 | ||||||
chrX:118778365 | C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+1854C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118778365 | ||||||
chrX:118778424 | G | A | 1 | a0001c0001t0007g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1191+1913G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118778424 | ||||||
chrX:118778474 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1191+1963C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118778474 | ||||||
chrX:118778878 | A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0126others(5): Show | 9 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1191+2367A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118778878 | ||||||
chrX:118778911 | C | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1191+2400C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118778911 | ||||||
chrX:118779374 | G | GT | 1 | a0001c0001t0001g0177 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1191+2866dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118779374 | |||||
chrX:118779377 | TA | T | 1 | a0001c0001t0001g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1191+2873delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118779377 | |||||
chrX:118779627 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1191+3116G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118779627 | ||||||
chrX:118779793 | G | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+3282G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118779793 | ||||||
chrX:118779866 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1191+3355G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118779866 | ||||||
chrX:118779948 | C | T | 4 | a0001c0001t0003g0062a0001c0001t0003g0102a0001c0001t0003g0103others(1): Show | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+3437C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118779948 | ||||||
chrX:118780171 | G | GA | 5 | a0001c0001t0001g0100a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3667dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118780171 | |||||
chrX:118780183 | C | CT | 3 | a0001c0001t0001g0095a0001c0001t0001g0263a0001c0001t0016g0252 | 3 | HG02809.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1191+3675dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118780183 | |||||
chrX:118780219 | T | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1191+3708T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118780219 | ||||||
chrX:118780493 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1191+3982G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118780493 | ||||||
chrX:118780531 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1191+4020T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118780531 | ||||||
chrX:118780535 | G | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+4024G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118780535 | ||||||
chrX:118780614 | G | A | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1191+4103G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118780614 | ||||||
chrX:118780634 | A | AG | 1 | a0001c0001t0001g0240 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1191+4128dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118780634 | |||||
chrX:118780692 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1191+4181T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118780692 | ||||||
chrX:118780898 | T | G | 1 | a0001c0001t0002g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1191+4387T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118780898 | ||||||
chrX:118781200 | T | TA | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 174 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1191+4699dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118781200 | |||||
chrX:118781353 | CT | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+4852delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118781353 | |||||
chrX:118781395 | C | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG02818.hp2 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1191+4884C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118781395 | ||||||
chrX:118781443 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1191+4932C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118781443 | ||||||
chrX:118781591 | G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+5080G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118781591 | ||||||
chrX:118781798 | A | G | 1 | a0001c0001t0012g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1191+5287A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118781798 | ||||||
chrX:118781869 | C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+5358C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118781869 | ||||||
chrX:118782255 | T | G | 4 | a0001c0001t0003g0062a0001c0001t0003g0102a0001c0001t0003g0103others(1): Show | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+5744T>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782255 | ||||||
chrX:118782327 | A | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+5816A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782327 | ||||||
chrX:118782328 | G | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+5817G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782328 | ||||||
chrX:118782329 | C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+5818C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782329 | ||||||
chrX:118782407 | T | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+5896T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782407 | ||||||
chrX:118782557 | A | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1191+6046A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782557 | ||||||
chrX:118782604 | C | CT | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1191+6104dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118782604 | |||||
chrX:118782604 | CT | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+6104delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118782604 | |||||
chrX:118782731 | G | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0147a0001c0001t0001g0158others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+6220G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782731 | ||||||
chrX:118782767 | A | AT | 1 | a0001c0001t0001g0261 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1191+6271dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118782767 | |||||
chrX:118782767 | AT | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(18): Show | 22 | HG01099.hp1 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1191+6271delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118782767 | |||||
chrX:118782767 | ATT | A | 1 | a0002c0003t0015g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1191+6270_1191+627 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118782767 | |||||
chrX:118782767 | ATTT | A | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1191+6269_1191+627 others(7): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118782767 | |||||
chrX:118782794 | C | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1191+6283C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118782794 | ||||||
chrX:118783649 | T | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0095others(23): Show | 28 | HG00621.hp1 HG00639.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1191+7138T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118783649 | ||||||
chrX:118783708 | G | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0049 | 3 | HG00735.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1191+7197G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118783708 | ||||||
chrX:118783755 | T | TAC | 1 | a0001c0001t0001g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1191+7263_1191+726 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783755 | T | TACAC | 131 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1191+7261_1191+726 others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783755 | T | TACACAC | 12 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0198others(9): Show | 12 | HG00323.hp2 HG00408.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.1191+7259_1191+726 others(10): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783755 | T | TACACACA others(1): Show |
5 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG01081.hp1 HG02257.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+7257_1191+726 others(12): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783755 | T | TACACACA others(3): Show |
88 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(85): Show | 92 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1191+7255_1191+726 others(14): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783755 | T | TACACACA others(5): Show |
16 | a0001c0001t0001g0006a0001c0001t0001g0095a0001c0001t0001g0115others(13): Show | 17 | HG00639.hp2 HG00642.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1191+7253_1191+726 others(16): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783755 | T | TACACACA others(7): Show |
7 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02970.hp1 HG02976.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1191+7251_1191+726 others(18): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783755 | T | TACACACA others(9): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0101 | 3 | HG02257.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1191+7249_1191+726 others(20): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783755 | |||||
chrX:118783765 | C | CACAA | 1 | a0001c0001t0001g0177 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1191+7257_1191+725 others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118783765 | |||||
chrX:118783854 | G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0162 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1191+7343G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118783854 | ||||||
chrX:118784025 | G | A | 1 | a0001c0001t0019g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1191+7514G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784025 | ||||||
chrX:118784075 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1191+7564G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784075 | ||||||
chrX:118784077 | C | CA | 17 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(14): Show | 18 | HG00621.hp1 HG00639.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1191+7580dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784077 | |||||
chrX:118784077 | CA | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0221others(4): Show | 8 | HG00558.hp1 HG01496.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1191+7580delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784077 | |||||
chrX:118784086 | A | AAT | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1191+7576_1191+757 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784086 | |||||
chrX:118784086 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1191+7575A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784086 | ||||||
chrX:118784088 | A | AAT | 7 | a0001c0001t0001g0157a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG00639.hp1 HG02257.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1191+7578_1191+757 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784088 | |||||
chrX:118784088 | A | AATATATA others(3): Show |
1 | a0001c0001t0002g0060 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1191+7578_1191+757 others(14): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784088 | |||||
chrX:118784088 | A | AT | 2 | a0001c0001t0001g0126a0001c0001t0012g0258 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1191+7577_1191+757 others(5): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784088 | ||||||
chrX:118784088 | A | ATATATAT others(2): Show |
1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+7577_1191+757 others(13): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784088 | ||||||
chrX:118784088 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0243 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1191+7577_1191+757 others(17): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784088 | ||||||
chrX:118784088 | A | T | 2 | a0001c0001t0001g0259a0001c0001t0016g0252 | 2 | HG01106.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1191+7577A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784088 | ||||||
chrX:118784089 | A | ATATATAT others(77): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0098 | 3 | HG01099.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1191+7578_1191+757 others(88): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784089 | ||||||
chrX:118784090 | A | AAAATATA others(5): Show |
12 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0015others(9): Show | 12 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1191+7580_1191+758 others(16): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784090 | |||||
chrX:118784090 | A | AAATATAT others(6): Show |
5 | a0001c0001t0002g0053a0001c0001t0002g0063a0001c0001t0002g0066others(2): Show | 5 | HG00544.hp1 NA18968.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+7580_1191+758 others(17): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784090 | |||||
chrX:118784090 | A | AAT | 2 | a0001c0001t0001g0270a0001c0002t0001g0142 | 2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1191+7597_1191+759 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784090 | |||||
chrX:118784090 | A | AATATATA others(5): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0039 | 3 | NA18939.hp2 NA18969.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1191+7587_1191+759 others(16): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784090 | |||||
chrX:118784090 | A | AT | 17 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0128others(14): Show | 18 | HG01123.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1191+7579_1191+758 others(5): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784090 | ||||||
chrX:118784090 | A | ATATATAT others(4): Show |
3 | a0001c0001t0002g0087a0001c0001t0002g0093a0001c0001t0018g0094 | 3 | HG01943.hp1 HG02293.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1191+7579_1191+758 others(15): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784090 | ||||||
chrX:118784090 | A | ATATATAT others(24): Show |
1 | a0001c0001t0002g0023 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1191+7579_1191+758 others(35): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784090 | ||||||
chrX:118784090 | A | ATATATAT others(6): Show |
15 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0022others(12): Show | 16 | HG00733.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1191+7579_1191+758 others(17): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784090 | ||||||
chrX:118784090 | A | ATATATAT others(26): Show |
1 | a0001c0001t0002g0028 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1191+7579_1191+758 others(37): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784090 | ||||||
chrX:118784090 | A | ATATATAT others(8): Show |
2 | a0001c0001t0002g0002a0001c0001t0002g0073 | 3 | HG00280.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1191+7579_1191+758 others(19): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784090 | ||||||
chrX:118784090 | A | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(56): Show | 62 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1191+7579A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784090 | ||||||
chrX:118784090 | AAT | A | 1 | a0001c0001t0001g0236 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1191+7597_1191+759 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784090 | |||||
chrX:118784091 | A | AATATATA others(86): Show |
1 | a0001c0001t0002g0074 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1191+7580_1191+758 others(97): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784091 | ||||||
chrX:118784091 | A | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0028 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1191+7580A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784091 | ||||||
chrX:118784092 | T | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0218 | 3 | HG02165.hp2 HG02809.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1191+7581T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784092 | ||||||
chrX:118784093 | A | ATATATAT others(67): Show |
1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1191+7590_1191+759 others(78): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784093 | |||||
chrX:118784093 | A | ATATATAT others(41): Show |
1 | a0001c0001t0012g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(52): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784093 | |||||
chrX:118784093 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(42): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784093 | |||||
chrX:118784093 | A | ATATATAT others(125): Show |
1 | a0001c0001t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(136): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784093 | |||||
chrX:118784093 | A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(54): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784093 | |||||
chrX:118784108 | T | C | 4 | a0001c0001t0001g0139a0001c0001t0002g0023a0001c0001t0002g0028others(1): Show | 4 | HG03209.hp1 HG03669.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+7597T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784108 | ||||||
chrX:118784108 | T | TATATATA others(79): Show |
2 | a0001c0001t0002g0029a0001c0001t0002g0047 | 2 | HG03831.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1191+7598_1191+759 others(90): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(81): Show |
5 | a0001c0001t0002g0021a0001c0001t0002g0061a0001c0001t0002g0064others(2): Show | 5 | NA18947.hp2 NA18972.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+7598_1191+759 others(92): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(81): Show |
1 | a0001c0001t0002g0065 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(92): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(77): Show |
1 | a0001c0001t0002g0027 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(88): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(81): Show |
1 | a0001c0001t0002g0032 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(92): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(81): Show |
20 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0026others(17): Show | 21 | HG00323.hp1 HG00408.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.1191+7598_1191+759 others(92): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(83): Show |
3 | a0001c0001t0002g0046a0001c0001t0002g0072a0001c0001t0002g0089 | 3 | HG02155.hp1 HG06807.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1191+7598_1191+759 others(94): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(83): Show |
1 | a0001c0001t0002g0038 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(94): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(85): Show |
4 | a0001c0001t0002g0017a0001c0001t0002g0044a0001c0001t0002g0050others(1): Show | 4 | HG02738.hp1 HG04204.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+7598_1191+759 others(96): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(87): Show |
1 | a0001c0001t0002g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(98): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(87): Show |
1 | a0001c0001t0002g0036 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(98): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784108 | T | TATATATA others(91): Show |
1 | a0001c0001t0002g0057 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1191+7598_1191+759 others(102): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784108 | |||||
chrX:118784119 | G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0184 | 2 | HG00323.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1191+7608G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784119 | ||||||
chrX:118784119 | G | GTA | 44 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0018others(41): Show | 45 | HG00323.hp1 HG00408.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.1191+7616_1191+761 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784119 | |||||
chrX:118784125 | A | ATACG | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0193 | 3 | NA18959.hp1 NA19058.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1191+7616_1191+761 others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784125 | |||||
chrX:118784127 | A | ACG | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1191+7616_1191+761 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784127 | ||||||
chrX:118784128 | T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 87 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1191+7617T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784128 | ||||||
chrX:118784129 | G | A | 5 | a0001c0001t0001g0086a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG02647.hp1 NA18612.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+7618G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784129 | ||||||
chrX:118784129 | G | GTA | 27 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0143others(24): Show | 27 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1192-7616_1192-761 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784129 | |||||
chrX:118784129 | G | GTATA | 88 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 92 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1192-7618_1192-761 others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784129 | |||||
chrX:118784129 | G | GTATATA | 5 | a0001c0001t0001g0213a0001c0001t0001g0217a0001c0001t0001g0229others(2): Show | 5 | HG01081.hp2 HG02602.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-7620_1192-761 others(10): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784129 | |||||
chrX:118784129 | G | GTATATAT others(1): Show |
1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1192-7622_1192-761 others(12): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784129 | |||||
chrX:118784129 | G | GTATATAT others(3): Show |
1 | a0001c0001t0008g0204 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1192-7624_1192-761 others(14): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784129 | |||||
chrX:118784129 | G | GTGTA | 1 | a0001c0001t0001g0250 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1191+7619_1191+762 others(8): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784129 | |||||
chrX:118784131 | A | G | 1 | a0001c0001t0002g0011 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1191+7620A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784131 | ||||||
chrX:118784138 | T | TACACAC | 51 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0097others(48): Show | 53 | HG00323.hp1 HG00408.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1192-7623_1192-762 others(10): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(35): Show |
5 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192-7617_1192-761 others(46): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(67): Show |
1 | a0004c0004t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1192-7617_1192-761 others(78): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(99): Show |
4 | a0001c0001t0003g0062a0001c0001t0003g0102a0001c0001t0003g0103others(1): Show | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-7617_1192-761 others(110): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(105): Show |
2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1192-7617_1192-761 others(116): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(77): Show |
8 | a0001c0001t0002g0040a0001c0001t0002g0054a0001c0001t0002g0058others(5): Show | 8 | HG00558.hp2 HG00642.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192-7615_1192-761 others(88): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(107): Show |
1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1192-7615_1192-761 others(118): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(79): Show |
10 | a0001c0001t0002g0002a0001c0001t0002g0022a0001c0001t0002g0024others(7): Show | 11 | HG00280.hp1 HG00544.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1192-7615_1192-761 others(90): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(81): Show |
9 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0048others(6): Show | 10 | HG00733.hp1 HG00735.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192-7615_1192-761 others(92): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(83): Show |
2 | a0001c0001t0002g0056a0001c0001t0002g0068 | 2 | HG01934.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1192-7615_1192-761 others(94): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(83): Show |
3 | a0001c0001t0002g0088a0001c0001t0002g0243a0007c0009t0002g0264 | 3 | HG02165.hp1 NA18965.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1192-7615_1192-761 others(94): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(79): Show |
1 | a0001c0001t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1192-7615_1192-761 others(90): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784138 | T | TATATATA others(125): Show |
1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1192-7615_1192-761 others(136): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784138 | |||||
chrX:118784149 | G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(95): Show | 102 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1192-7613G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784149 | ||||||
chrX:118784149 | G | GTATATAT others(71): Show |
1 | a0001c0001t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1192-7607_1192-760 others(82): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784149 | |||||
chrX:118784149 | G | GTATATAT others(69): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 7 | HG00639.hp2 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1192-7607_1192-760 others(80): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784149 | |||||
chrX:118784149 | G | GTATATAT others(75): Show |
9 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(6): Show | 9 | HG00423.hp1 HG01993.hp2 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1192-7607_1192-760 others(86): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784149 | |||||
chrX:118784149 | G | GTATATAT others(71): Show |
4 | a0001c0001t0001g0115a0001c0001t0001g0126a0001c0001t0001g0131others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-7607_1192-760 others(82): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784149 | |||||
chrX:118784149 | G | GTATATAT others(105): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0128others(4): Show | 8 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192-7607_1192-760 others(116): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784149 | |||||
chrX:118784149 | G | GTATATAT others(77): Show |
1 | a0001c0001t0002g0060 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1192-7607_1192-760 others(88): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784149 | |||||
chrX:118784161 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1192-7601A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784161 | ||||||
chrX:118784167 | G | A | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1192-7595G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784167 | ||||||
chrX:118784240 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1192-7522G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784240 | ||||||
chrX:118784324 | G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1192-7438G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784324 | ||||||
chrX:118784349 | C | T | 1 | a0002c0003t0001g0122 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1192-7413C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784349 | ||||||
chrX:118784476 | TTAA | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 7 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1192-7284_1192-728 others(7): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118784476 | |||||
chrX:118784668 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1192-7094C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784668 | ||||||
chrX:118784800 | G | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1192-6962G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784800 | ||||||
chrX:118784804 | C | T | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0265others(5): Show | 8 | HG02257.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192-6958C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784804 | ||||||
chrX:118784863 | G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0101others(16): Show | 21 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1192-6899G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784863 | ||||||
chrX:118784967 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1192-6795C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118784967 | ||||||
chrX:118785006 | A | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1192-6756A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118785006 | ||||||
chrX:118785019 | TC | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02155.hp2 NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1192-6742delC | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118785019 | ||||||
chrX:118785020 | CT | C | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1192-6731delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118785020 | |||||
chrX:118785342 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1192-6420A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118785342 | ||||||
chrX:118785794 | C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0095others(23): Show | 28 | HG00621.hp1 HG00639.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1192-5968C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118785794 | ||||||
chrX:118785955 | A | T | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1192-5807A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118785955 | ||||||
chrX:118786047 | G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 5 | HG00558.hp1 HG01496.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192-5715G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118786047 | ||||||
chrX:118786172 | C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1192-5590C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118786172 | ||||||
chrX:118786241 | A | AT | 1 | a0001c0001t0001g0226 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1192-5519dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118786241 | |||||
chrX:118786246 | C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1192-5516C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118786246 | ||||||
chrX:118786390 | C | CA | 3 | a0001c0001t0001g0118a0001c0001t0001g0261a0001c0001t0002g0064 | 3 | HG02145.hp1 NA19006.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1192-5358dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118786390 | |||||
chrX:118786484 | C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1192-5278C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118786484 | ||||||
chrX:118786645 | A | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1192-5117A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118786645 | ||||||
chrX:118786692 | C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1192-5070C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118786692 | ||||||
chrX:118787062 | TG | T | 1 | a0002c0003t0015g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192-4695delG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118787062 | |||||
chrX:118787154 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1192-4608A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787154 | ||||||
chrX:118787292 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1192-4470C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787292 | ||||||
chrX:118787475 | G | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1192-4287G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787475 | ||||||
chrX:118787603 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1192-4159G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787603 | ||||||
chrX:118787775 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1192-3987T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787775 | ||||||
chrX:118787946 | C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0195a0001c0001t0006g0200 | 3 | NA18747.hp1 NA19055.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1192-3816C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787946 | ||||||
chrX:118787969 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1192-3793A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787969 | ||||||
chrX:118787975 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1192-3787C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118787975 | ||||||
chrX:118787987 | AT | A | 1 | a0001c0001t0002g0037 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1192-3773delT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118787987 | |||||
chrX:118788090 | G | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1192-3672G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118788090 | ||||||
chrX:118788095 | G | A | 7 | a0001c0001t0001g0100a0001c0001t0001g0120a0001c0001t0001g0121others(4): Show | 7 | HG00099.hp2 HG01243.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1192-3667G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118788095 | ||||||
chrX:118788120 | T | TG | 1 | a0002c0003t0015g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192-3640dupG | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118788120 | |||||
chrX:118788180 | G | T | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1192-3582G>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118788180 | ||||||
chrX:118788192 | G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 5 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1192-3570G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118788192 | ||||||
chrX:118788453 | A | AT | 1 | a0002c0003t0015g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192-3306dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118788453 | |||||
chrX:118788518 | A | T | 1 | a0001c0001t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1192-3244A>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118788518 | ||||||
chrX:118788557 | A | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1192-3205A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118788557 | ||||||
chrX:118788742 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1192-3020C>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118788742 | ||||||
chrX:118789024 | CA | C | 1 | a0002c0003t0015g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192-2734delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118789024 | |||||
chrX:118789150 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1192-2612T>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118789150 | ||||||
chrX:118789183 | G | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0149a0001c0001t0001g0157others(5): Show | 8 | HG00639.hp1 HG00733.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192-2579G>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118789183 | ||||||
chrX:118789423 | A | G | 5 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0174others(2): Show | 5 | NA18960.hp1 NA18967.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-2339A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118789423 | ||||||
chrX:118789548 | A | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1192-2214A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118789548 | ||||||
chrX:118789792 | A | AT | 1 | a0001c0001t0001g0239 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1192-1962dupT | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118789792 | |||||
chrX:118789889 | C | G | 255 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 265 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1192-1873C>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118789889 | ||||||
chrX:118790134 | A | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1192-1628A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118790134 | ||||||
chrX:118790398 | CAG | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0254 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1192-1361_1192-136 others(6): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118790398 | |||||
chrX:118790499 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1192-1263C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118790499 | ||||||
chrX:118790653 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1192-1109G>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118790653 | ||||||
chrX:118790844 | A | C | 17 | a0001c0001t0002g0021a0001c0001t0002g0048a0001c0001t0002g0051others(14): Show | 17 | HG00544.hp1 HG00738.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.1192-918A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118790844 | ||||||
chrX:118791070 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1192-692A>G | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118791070 | ||||||
chrX:118791280 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1192-482C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118791280 | ||||||
chrX:118791289 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1192-473C>T | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118791289 | ||||||
chrX:118791330 | T | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1192-432T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118791330 | ||||||
chrX:118791409 | T | A | 2 | a0001c0001t0004g0166a0001c0001t0004g0225 | 2 | NA18980.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1192-353T>A | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118791409 | ||||||
chrX:118791591 | A | C | 1 | a0001c0001t0016g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1192-171A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118791591 | ||||||
chrX:118791621 | C | CA | 13 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0146others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-125dupA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118791621 | |||||
chrX:118791621 | CA | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(25): Show | 31 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1192-125delA | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118791621 | |||||
chrX:118791621 | CAA | C | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1192-126_1192-125d others(4): Show |
IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 118791621 | |||||
chrX:118791639 | A | C | 4 | a0001c0001t0003g0062a0001c0001t0003g0102a0001c0001t0003g0103others(1): Show | 4 | HG00621.hp1 HG03688.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-123A>C | IL13RA1 | ENSG00000131724.11 | transcript | ENST00000371666.8 | protein_coding | 10/10 | chrX | 118791639 |