geneid | 389668 |
---|---|
ensemblid | ENSG00000221947.8 |
hgncid | 20937 |
symbol | XKR9 |
name | XK related 9 |
refseq_nuc | NM_001011720.2 |
refseq_prot | NP_001011720.1 |
ensembl_nuc | ENST00000408926.8 |
ensembl_prot | ENSP00000386141.3 |
mane_status | MANE Select |
chr | chr8 |
start | 70669339 |
end | 70735942 |
strand | + |
ver | v1.2 |
region | chr8:70669339-70735942 |
region5000 | chr8:70664339-70740942 |
regionname0 | XKR9_chr8_70669339_70735942 |
regionname5000 | XKR9_chr8_70664339_70740942 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 373 | 313 | 80 | 57 | 136 | 10 | 28 | 110 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0002 | 0/0 | 373 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0003 | 0/0 | 182 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0004 | 0/0 | 373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0005 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1122 | 212 | 54 | 37 | 98 | 5 | 17 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0002 | 0/1 | 1122 | 86 | 22 | 19 | 31 | 4 | 9 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0003 | 0/0 | 1122 | 7 | 0 | 0 | 7 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0004 | 0/0 | 1122 | 5 | 5 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0005 | 0/0 | 1122 | 4 | 0 | 1 | 0 | 1 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0006 | 0/0 | 1122 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0007 | 0/0 | 1122 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0008 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
c0009 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2079 | 108 | 22 | 13 | 56 | 4 | 12 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0002 | 0/1 | 2079 | 72 | 15 | 14 | 31 | 4 | 7 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0003 | 0/0 | 2079 | 57 | 0 | 12 | 43 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0004 | 0/0 | 2079 | 36 | 20 | 11 | 1 | 1 | 3 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0005 | 0/0 | 2079 | 9 | 2 | 5 | 0 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0006 | 0/0 | 2079 | 5 | 1 | 1 | 0 | 1 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0007 | 0/0 | 2079 | 5 | 5 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0008 | 0/0 | 2076 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0009 | 0/0 | 2078 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0010 | 0/0 | 2075 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0011 | 0/0 | 2079 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0012 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0013 | 0/0 | 2079 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0014 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0015 | 0/0 | 2072 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0016 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0017 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0018 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0019 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0020 | 0/0 | 2078 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0021 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0022 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0023 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0024 | 0/0 | 2079 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
t0025 | 0/0 | 2079 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0026 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1122 | 212 | 54 | 37 | 98 | 5 | 17 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0002 | 0/1 | 1122 | 86 | 22 | 19 | 31 | 4 | 9 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0003 | 0/0 | 1122 | 7 | 0 | 0 | 7 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0005 | 0/0 | 1122 | 4 | 0 | 1 | 0 | 1 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0006 | 0/0 | 1122 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0002c0004 | 0/0 | 1122 | 5 | 5 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0003c0007 | 0/0 | 1122 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0004c0008 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0005c0009 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3200 | 106 | 22 | 13 | 54 | 4 | 12 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0003 | 0/0 | 3200 | 50 | 0 | 12 | 36 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0004 | 0/0 | 3200 | 35 | 19 | 11 | 1 | 1 | 3 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0006 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0007 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0010 | 0/0 | 3196 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0011 | 0/0 | 3200 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0012 | 0/0 | 3196 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0013 | 0/0 | 3200 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0014 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0015 | 0/0 | 3193 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0016 | 0/0 | 3197 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0017 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0018 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0019 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0020 | 0/0 | 3199 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0021 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0001t0025 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0002t0002 | 0/1 | 3200 | 70 | 14 | 13 | 31 | 4 | 7 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0002t0005 | 0/0 | 3200 | 9 | 2 | 5 | 0 | 0 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0002t0008 | 0/0 | 3197 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0002t0022 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0002t0023 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0002t0024 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0003t0003 | 0/0 | 3200 | 7 | 0 | 0 | 7 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0005t0006 | 0/0 | 3200 | 4 | 0 | 1 | 0 | 1 | 2 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0001c0006t0007 | 0/0 | 3200 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0002c0004t0002 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0002c0004t0009 | 0/0 | 3199 | 4 | 4 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0003c0007t0001 | 0/0 | 3200 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0004c0008t0002 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
a0005c0009t0004 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | copy fasta | chr8 | 70664339 | 70740942 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0014g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0015g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0017g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0018g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0019g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0020g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0021g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0001t0025g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0026 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0022g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0023g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0002t0024g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0003t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0003t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0005t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0005t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0005t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0005t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0006t0007g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0001c0006t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0002c0004t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0002c0004t0009g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0002c0004t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0002c0004t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0002c0004t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0003c0007t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0003c0007t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0004c0008t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
a0005c0009t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0006 | g0161 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0230 | EUR | GBR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00639 | hp2 | a0001 | c0005 | t0006 | g0162 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00642 | hp1 | a0001 | c0002 | t0005 | g0238 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0247 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01074 | hp2 | a0001 | c0002 | t0005 | g0239 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01168 | hp1 | a0001 | c0002 | t0005 | g0024 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0250 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01169 | hp2 | a0001 | c0002 | t0005 | g0024 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0276 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0281 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01256 | hp1 | a0004 | c0008 | t0002 | g0271 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01258 | hp2 | a0001 | c0002 | t0024 | g0232 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0233 | EUR | IBS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0283 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0260 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0280 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02004 | hp1 | a0001 | c0002 | t0005 | g0237 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0207 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02056 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02074 | hp2 | a0001 | c0001 | t0014 | g0134 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02132 | hp1 | a0001 | c0001 | t0011 | g0067 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02135 | hp1 | a0001 | c0001 | t0021 | g0048 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02148 | hp1 | a0001 | c0001 | t0025 | g0006 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02165 | hp2 | a0001 | c0003 | t0003 | g0146 | EAS | CDX | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02258 | hp1 | a0001 | c0002 | t0023 | g0245 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02451 | hp1 | a0001 | c0006 | t0007 | g0007 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02451 | hp2 | a0001 | c0001 | t0010 | g0203 | AFR | ACB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02615 | hp2 | a0001 | c0006 | t0007 | g0007 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02622 | hp2 | a0001 | c0002 | t0005 | g0259 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02717 | hp1 | a0001 | c0002 | t0022 | g0253 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02735 | hp1 | a0001 | c0005 | t0006 | g0164 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0258 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0262 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0052 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02897 | hp2 | a0001 | c0006 | t0007 | g0157 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02965 | hp1 | a0001 | c0001 | t0010 | g0205 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02965 | hp2 | a0001 | c0002 | t0008 | g0209 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0265 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02970 | hp2 | a0001 | c0006 | t0007 | g0007 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0204 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0234 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0263 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03098 | hp2 | a0001 | c0002 | t0008 | g0241 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0266 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03195 | hp1 | a0001 | c0001 | t0016 | g0045 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03209 | hp1 | a0002 | c0004 | t0009 | g0274 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0279 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03453 | hp2 | a0002 | c0004 | t0009 | g0272 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03486 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0277 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03492 | hp1 | a0001 | c0002 | t0005 | g0240 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03516 | hp1 | a0002 | c0004 | t0009 | g0273 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03516 | hp2 | a0001 | c0002 | t0008 | g0208 | AFR | ESN | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | GWD | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03579 | hp1 | a0001 | c0001 | t0015 | g0201 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03704 | hp1 | a0001 | c0005 | t0006 | g0163 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0035 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0243 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0244 | SAS | BEB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18522 | hp1 | a0005 | c0009 | t0004 | g0166 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18522 | hp2 | a0002 | c0004 | t0002 | g0264 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CHB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0278 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18952 | hp1 | a0001 | c0001 | t0011 | g0118 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18952 | hp2 | a0001 | c0001 | t0020 | g0111 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18968 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18981 | hp2 | a0001 | c0003 | t0003 | g0156 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18982 | hp2 | a0001 | c0001 | t0019 | g0181 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18991 | hp2 | a0001 | c0001 | t0011 | g0176 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18993 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19030 | hp1 | a0001 | c0002 | t0005 | g0261 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19062 | hp1 | a0003 | c0007 | t0001 | g0085 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19068 | hp2 | a0001 | c0003 | t0003 | g0139 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19070 | hp1 | a0001 | c0003 | t0003 | g0141 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19084 | hp2 | a0003 | c0007 | t0001 | g0088 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0252 | AFR | ASW | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ASW | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0246 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0026 | EUR | TSI | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | GIH | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG03471 | hp2 | a0001 | c0002 | t0008 | g0210 | AFR | MSL | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
HG06807 | hp2 | a0001 | c0001 | t0017 | g0030 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA20300 | hp2 | a0002 | c0004 | t0009 | g0275 | AFR | USA | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA21309 | hp1 | a0001 | c0001 | t0013 | g0051 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0026 | REF | REF | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0160 | REF | REF | XKR9_chr8_70664339_70740942 | XKR9 | chr8 | 70664339 | 70740942 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:70707000
|
G | T | 1 | a0002 | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
missense_variant | MODERATE | c.340G>T | p.Val114Leu | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/5 | 900/3200 | 340/1122 | 114/373 | chr8 | 70707000 | ||
chr8:70707037
|
A | G | 1 | a0005 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.377A>G | p.Asp126Gly | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/5 | 937/3200 | 377/1122 | 126/373 | chr8 | 70707037 | ||
chr8:70733849
|
C | T | 1 | a0003 | 2 | NA19062.hp1 NA19084.hp2 |
stop_gained | HIGH | c.547C>T | p.Gln183* | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1107/3200 | 547/1122 | 183/373 | chr8 | 70733849 | ||
chr8:70733877
|
A | T | 1 | a0004 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.575A>T | p.Asp192Val | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1135/3200 | 575/1122 | 192/373 | chr8 | 70733877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:70681190
|
G | A | 3 | a0001c0002a0002c0004a0004c0008 | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
synonymous_variant | LOW | c.132G>A | p.Ala44Ala | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 692/3200 | 132/1122 | 44/373 | chr8 | 70681190 | ||
chr8:70707018
|
C | T | 1 | a0001c0006 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.358C>T | p.Leu120Leu | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/5 | 918/3200 | 358/1122 | 120/373 | chr8 | 70707018 | ||
chr8:70734226
|
C | T | 1 | a0001c0005 | 4 | HG00099.hp1 HG00639.hp2 HG02735.hp1 others(1): Show |
synonymous_variant | LOW | c.924C>T | p.Cys308Cys | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1484/3200 | 924/1122 | 308/373 | chr8 | 70734226 | ||
chr8:70734241
|
T | C | 1 | a0001c0003 | 7 | HG02056.hp2 HG02165.hp2 NA18968.hp1 others(4): Show |
synonymous_variant | LOW | c.939T>C | p.Phe313Phe | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1499/3200 | 939/1122 | 313/373 | chr8 | 70734241 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:70680840
|
A | G | 1 | a0001c0001t0025 | 1 | HG02148.hp1 | 5_prime_UTR_variant | MODIFIER | c.-219A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 219 | chr8 | 70680840 | |||||
chr8:70680929
|
C | T | 1 | a0001c0002t0024 | 1 | HG01258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 130 | chr8 | 70680929 | |||||
chr8:70680963
|
A | G | 7 | a0001c0002t0002a0001c0002t0022a0001c0002t0023others(4): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-96A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/5 | 96 | chr8 | 70680963 | |||||
chr8:70734442
|
T | C | 1 | a0001c0001t0014 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 18 | chr8 | 70734442 | |||||
chr8:70734445
|
A | G | 1 | a0001c0002t0023 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 21 | chr8 | 70734445 | |||||
chr8:70734606
|
A | T | 1 | a0001c0001t0021 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 182 | chr8 | 70734606 | |||||
chr8:70734651
|
TC | T | 1 | a0002c0004t0009 | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*228delC | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 228 | chr8 | 70734651 | |||||
chr8:70734673
|
A | G | 1 | a0001c0001t0013 | 2 | HG02895.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*249A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 249 | chr8 | 70734673 | |||||
chr8:70734745
|
T | C | 7 | a0001c0002t0002a0001c0002t0022a0001c0002t0023others(4): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 321 | chr8 | 70734745 | |||||
chr8:70734974
|
G | GACCTCTC others(11): Show |
1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552_*553insCTCTCA others(12): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 553 | INFO_REALIGN_3_PRIME | chr8 | 70734974 | ||||
chr8:70734982
|
A | T | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 558 | chr8 | 70734982 | |||||
chr8:70734986
|
T | C | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*562T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 562 | chr8 | 70734986 | |||||
chr8:70734992
|
T | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 568 | chr8 | 70734992 | |||||
chr8:70734994
|
T | A | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 570 | chr8 | 70734994 | |||||
chr8:70734998
|
C | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*574C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 574 | chr8 | 70734998 | |||||
chr8:70734999
|
T | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 575 | chr8 | 70734999 | |||||
chr8:70735010
|
A | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*586A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 586 | chr8 | 70735010 | |||||
chr8:70735016
|
T | A | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 592 | chr8 | 70735016 | |||||
chr8:70735023
|
T | C | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 599 | chr8 | 70735023 | |||||
chr8:70735026
|
A | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*602A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 602 | chr8 | 70735026 | |||||
chr8:70735029
|
T | G | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 605 | chr8 | 70735029 | |||||
chr8:70735030
|
ATAATTAT others(12): Show |
A | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*608_*626delAATTAT others(13): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 608 | INFO_REALIGN_3_PRIME | chr8 | 70735030 | ||||
chr8:70735051
|
G | T | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*627G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 627 | chr8 | 70735051 | |||||
chr8:70735125
|
A | G | 2 | a0001c0002t0005a0001c0002t0008 | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*701A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 701 | chr8 | 70735125 | |||||
chr8:70735202
|
G | A | 1 | a0001c0002t0005 | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*778G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 778 | chr8 | 70735202 | |||||
chr8:70735204
|
C | A | 1 | a0001c0002t0022 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 780 | chr8 | 70735204 | |||||
chr8:70735232
|
CTATT | C | 3 | a0001c0001t0010a0001c0001t0012a0001c0001t0015 | 6 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*813_*816delTATT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 813 | INFO_REALIGN_3_PRIME | chr8 | 70735232 | ||||
chr8:70735364
|
A | T | 1 | a0001c0001t0019 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*940A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 940 | chr8 | 70735364 | |||||
chr8:70735370
|
G | T | 26 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(23): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*946G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 946 | chr8 | 70735370 | |||||
chr8:70735459
|
ATAT | A | 3 | a0001c0001t0015a0001c0001t0016a0001c0002t0008 | 6 | HG02965.hp2 HG03098.hp2 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1054_*1056delTAT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1054 | INFO_REALIGN_3_PRIME | chr8 | 70735459 | ||||
chr8:70735578
|
T | G | 2 | a0001c0002t0005a0001c0002t0008 | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1154T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1154 | chr8 | 70735578 | |||||
chr8:70735620
|
C | A | 2 | a0001c0001t0011a0001c0001t0021 | 4 | HG02132.hp1 HG02135.hp1 NA18952.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1196C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1196 | chr8 | 70735620 | |||||
chr8:70735641
|
G | T | 1 | a0001c0001t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1217G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1217 | chr8 | 70735641 | |||||
chr8:70735679
|
G | A | 4 | a0001c0001t0003a0001c0001t0014a0001c0001t0025others(1): Show | 59 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1255G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1255 | chr8 | 70735679 | |||||
chr8:70735731
|
G | A | 3 | a0001c0001t0010a0001c0001t0012a0001c0001t0015 | 6 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1307 | chr8 | 70735731 | |||||
chr8:70735830
|
A | C | 2 | a0001c0001t0016a0001c0001t0017 | 2 | HG03195.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1406A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1406 | chr8 | 70735830 | |||||
chr8:70735861
|
T | C | 1 | a0001c0001t0010 | 3 | HG02451.hp2 HG02965.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1437T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1437 | chr8 | 70735861 | |||||
chr8:70735912
|
T | C | 5 | a0001c0001t0004a0001c0001t0013a0001c0001t0016others(2): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1488T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1488 | chr8 | 70735912 | |||||
chr8:70735933
|
T | C | 2 | a0001c0001t0006a0001c0005t0006 | 5 | HG00099.hp1 HG00639.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1509T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 5/5 | 1509 | chr8 | 70735933 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:70669606
|
C | CTG | 2 | a0001c0001t0003g0022a0001c0001t0003g0202 | 3 | HG00735.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-361+100_-361+101d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669606 | |||||
chr8:70669606
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0003g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-361+92_-361+101de others(11): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669606 | |||||
chr8:70669606
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0006g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-361+88_-361+101de others(15): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669606 | |||||
chr8:70669635
|
TGTGTA | T | 17 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0031others(14): Show | 19 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-361+100_-361+104d others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669635 | |||||
chr8:70669637
|
TGTA | T | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 95 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-361+116_-361+118d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669637 | |||||
chr8:70669639
|
T | TG | 29 | a0001c0001t0001g0206a0001c0001t0010g0203a0001c0001t0010g0204others(26): Show | 32 | HG00621.hp2 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | ||||||
chr8:70669639
|
T | TGTG | 9 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0027others(6): Show | 12 | HG02738.hp2 HG02922.hp1 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | ||||||
chr8:70669639
|
T | TGTGTG | 7 | a0001c0001t0007g0260a0001c0002t0002g0267a0001c0002t0002g0268others(4): Show | 7 | HG01256.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | ||||||
chr8:70669639
|
T | TGTGTGTG | 8 | a0001c0002t0002g0276a0001c0002t0002g0277a0001c0002t0002g0278others(5): Show | 8 | HG01243.hp1 HG03209.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.-361+101_-361+102i others(9): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | ||||||
chr8:70669639
|
TA | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0170others(38): Show | 44 | HG00673.hp2 HG01167.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.-361+102delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669639 | ||||||
chr8:70669640
|
A | G | 31 | a0001c0002t0002g0009a0001c0002t0002g0023a0001c0002t0002g0211others(28): Show | 34 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-361+102A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669640 | ||||||
chr8:70669640
|
A | T | 55 | a0001c0001t0001g0206a0001c0001t0007g0260a0001c0001t0010g0203others(52): Show | 61 | HG00621.hp2 HG00642.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-361+102A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669640 | ||||||
chr8:70669641
|
G | T | 31 | a0001c0002t0002g0009a0001c0002t0002g0023a0001c0002t0002g0211others(28): Show | 34 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-361+103G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669641 | ||||||
chr8:70669642
|
T | G | 31 | a0001c0002t0002g0009a0001c0002t0002g0023a0001c0002t0002g0211others(28): Show | 34 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-361+104T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | ||||||
chr8:70669642
|
T | TG | 48 | a0001c0002t0002g0010a0001c0002t0002g0025a0001c0002t0002g0026others(45): Show | 54 | HG00642.hp1 HG00733.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.-361+104_-361+105i others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | ||||||
chr8:70669642
|
T | TGTGTGTG others(16): Show |
1 | a0001c0002t0002g0280 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-361+104_-361+105i others(25): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | ||||||
chr8:70669642
|
T | TGTGTGTG others(18): Show |
1 | a0001c0002t0002g0281 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-361+104_-361+105i others(27): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669642 | ||||||
chr8:70669643
|
A | T | 81 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(78): Show | 90 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.-361+105A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669643 | ||||||
chr8:70669664
|
A | AT | 10 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0004g0044others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-361+146dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | |||||
chr8:70669664
|
A | ATT | 100 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(97): Show | 108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-361+145_-361+146d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | |||||
chr8:70669664
|
AT | A | 102 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0005others(99): Show | 118 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-361+146delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | |||||
chr8:70669664
|
ATT | A | 10 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0126others(7): Show | 15 | HG00735.hp1 HG01978.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.-361+145_-361+146d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | |||||
chr8:70669664
|
ATTT | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-361+144_-361+146d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70669664 | |||||
chr8:70669747
|
A | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-361+209A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669747 | ||||||
chr8:70669774
|
C | T | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-361+236C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669774 | ||||||
chr8:70669956
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-361+418A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70669956 | ||||||
chr8:70670131
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-361+593A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670131 | ||||||
chr8:70670244
|
TGCCTGCC others(25): Show |
T | 1 | a0001c0001t0016g0045 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-361+710_-361+741d others(34): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70670244 | |||||
chr8:70670355
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-361+817C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670355 | ||||||
chr8:70670356
|
A | C | 28 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(25): Show | 32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-361+818A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670356 | ||||||
chr8:70670423
|
C | T | 1 | a0001c0001t0013g0052 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-361+885C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670423 | ||||||
chr8:70670446
|
T | C | 1 | a0001c0001t0011g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-361+908T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670446 | ||||||
chr8:70670509
|
CT | C | 12 | a0001c0002t0002g0228a0001c0002t0002g0254a0001c0002t0002g0255others(9): Show | 12 | HG02630.hp1 HG02717.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-361+982delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70670509 | |||||
chr8:70670518
|
T | A | 1 | a0001c0002t0005g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-361+980T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670518 | ||||||
chr8:70670519
|
T | A | 11 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(8): Show | 12 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-361+981T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670519 | ||||||
chr8:70670519
|
T | TA | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-361+981_-361+982i others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670519 | ||||||
chr8:70670520
|
T | A | 219 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(216): Show | 242 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-361+982T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670520 | ||||||
chr8:70670528
|
G | A | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.-361+990G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670528 | ||||||
chr8:70670621
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18939.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-361+1083C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670621 | ||||||
chr8:70670838
|
T | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-361+1300T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670838 | ||||||
chr8:70670843
|
C | G | 3 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266 | 3 | HG02630.hp1 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-361+1305C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670843 | ||||||
chr8:70670861
|
G | A | 2 | a0001c0002t0002g0280a0001c0002t0002g0281 | 2 | HG01255.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-361+1323G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70670861 | ||||||
chr8:70671032
|
T | G | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-361+1494T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671032 | ||||||
chr8:70671075
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-361+1537G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671075 | ||||||
chr8:70671288
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 10 | HG02165.hp1 NA18612.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.-361+1750A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671288 | ||||||
chr8:70671320
|
CATGATCT others(1081): Show |
C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-361+1799_-360-239 others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671320 | |||||
chr8:70671329
|
ATT | A | 63 | a0001c0001t0001g0113a0001c0001t0001g0199a0001c0001t0001g0200others(60): Show | 79 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-361+1806_-361+180 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671329 | |||||
chr8:70671329
|
ATTT | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(127): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-361+1805_-361+180 others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671329 | |||||
chr8:70671329
|
ATTTT | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0170others(2): Show | 8 | HG01891.hp1 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-361+1804_-361+180 others(8): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70671329 | |||||
chr8:70671394
|
A | G | 1 | a0001c0001t0004g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-361+1856A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671394 | ||||||
chr8:70671425
|
T | C | 1 | a0001c0001t0013g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-361+1887T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671425 | ||||||
chr8:70671557
|
C | A | 2 | a0001c0001t0004g0011a0001c0001t0004g0044 | 3 | HG02145.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-361+2019C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671557 | ||||||
chr8:70671725
|
A | G | 149 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(146): Show | 161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-361+2187A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671725 | ||||||
chr8:70671923
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-361+2385C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70671923 | ||||||
chr8:70672044
|
A | G | 1 | a0001c0001t0020g0111 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-361+2506A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672044 | ||||||
chr8:70672083
|
T | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0133 | 3 | NA18944.hp1 NA18965.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-361+2545T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672083 | ||||||
chr8:70672125
|
G | A | 4 | a0001c0001t0004g0014a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 5 | HG02055.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-361+2587G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672125 | ||||||
chr8:70672256
|
T | C | 1 | a0001c0001t0007g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-360-2562T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672256 | ||||||
chr8:70672606
|
C | CTG | 5 | a0001c0001t0001g0113a0001c0001t0007g0260a0001c0001t0013g0051others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-360-2194_-360-219 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 70672606 | |||||
chr8:70672768
|
AG | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0113 | 3 | HG03704.hp2 HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-360-2049delG | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672768 | ||||||
chr8:70672933
|
T | A | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-360-1885T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672933 | ||||||
chr8:70672934
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-360-1884T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70672934 | ||||||
chr8:70673218
|
G | C | 1 | a0001c0002t0008g0208 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-360-1600G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673218 | ||||||
chr8:70673374
|
G | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-360-1444G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673374 | ||||||
chr8:70673475
|
G | A | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-360-1343G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673475 | ||||||
chr8:70673524
|
C | T | 1 | a0001c0001t0018g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-360-1294C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673524 | ||||||
chr8:70673694
|
G | A | 1 | a0001c0002t0002g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-360-1124G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673694 | ||||||
chr8:70673721
|
C | T | 2 | a0001c0001t0007g0260a0001c0001t0018g0207 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-360-1097C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673721 | ||||||
chr8:70673824
|
G | C | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.-360-994G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673824 | ||||||
chr8:70673917
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-360-901G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70673917 | ||||||
chr8:70674348
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-360-470C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674348 | ||||||
chr8:70674501
|
T | A | 2 | a0001c0001t0007g0260a0001c0001t0018g0207 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-360-317T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674501 | ||||||
chr8:70674659
|
C | A | 1 | a0001c0002t0002g0229 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-360-159C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674659 | ||||||
chr8:70674736
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-360-82A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 1/4 | chr8 | 70674736 | ||||||
chr8:70674908
|
A | G | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-279+9A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70674908 | ||||||
chr8:70675012
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-279+113C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675012 | ||||||
chr8:70675025
|
G | A | 1 | a0001c0001t0004g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-279+126G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675025 | ||||||
chr8:70675041
|
A | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-279+142A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675041 | ||||||
chr8:70675076
|
G | A | 1 | a0001c0001t0014g0134 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-279+177G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675076 | ||||||
chr8:70675162
|
C | T | 1 | a0001c0001t0006g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-279+263C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675162 | ||||||
chr8:70675187
|
G | A | 1 | a0001c0001t0001g0015 | 2 | NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-279+288G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675187 | ||||||
chr8:70675235
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-279+336G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675235 | ||||||
chr8:70675331
|
G | T | 1 | a0001c0001t0003g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-279+432G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675331 | ||||||
chr8:70675441
|
C | T | 1 | a0001c0003t0003g0156 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-279+542C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675441 | ||||||
chr8:70675458
|
T | C | 1 | a0001c0001t0012g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-279+559T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675458 | ||||||
chr8:70675474
|
C | G | 2 | a0002c0004t0009g0273a0002c0004t0009g0274 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-279+575C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675474 | ||||||
chr8:70675666
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-279+767A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675666 | ||||||
chr8:70675899
|
T | A | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1000T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675899 | ||||||
chr8:70675900
|
T | G | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1001T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675900 | ||||||
chr8:70675902
|
C | A | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1003C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675902 | ||||||
chr8:70675903
|
T | A | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+1004T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70675903 | ||||||
chr8:70676134
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-279+1235G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676134 | ||||||
chr8:70676151
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-279+1252T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676151 | ||||||
chr8:70676159
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-279+1260G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676159 | ||||||
chr8:70676191
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-279+1292G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676191 | ||||||
chr8:70676422
|
G | A | 4 | a0001c0001t0004g0014a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 5 | HG02055.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-279+1523G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676422 | ||||||
chr8:70676845
|
TAAAC | T | 6 | a0001c0001t0001g0112a0002c0004t0002g0264a0002c0004t0009g0272others(3): Show | 6 | HG01074.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-279+1965_-279+196 others(8): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70676845 | |||||
chr8:70676973
|
G | A | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-279+2074G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70676973 | ||||||
chr8:70677041
|
G | A | 1 | a0001c0002t0002g0267 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-279+2142G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677041 | ||||||
chr8:70677126
|
T | TA | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-279+2236dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70677126 | |||||
chr8:70677126
|
TA | T | 105 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-279+2236delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70677126 | |||||
chr8:70677171
|
G | GGTCTCAC others(28): Show |
3 | a0001c0001t0004g0012a0001c0001t0004g0041a0001c0001t0004g0042 | 4 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-279+2274_-279+230 others(39): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 70677171 | |||||
chr8:70677249
|
G | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0133 | 3 | NA18944.hp1 NA18965.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-279+2350G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677249 | ||||||
chr8:70677369
|
A | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-279+2470A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677369 | ||||||
chr8:70677414
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-279+2515C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677414 | ||||||
chr8:70677790
|
A | C | 1 | a0001c0001t0011g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-279+2891A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677790 | ||||||
chr8:70677916
|
A | G | 1 | a0001c0002t0002g0027 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-278-2865A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70677916 | ||||||
chr8:70678123
|
C | T | 1 | a0001c0002t0008g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-278-2658C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678123 | ||||||
chr8:70678208
|
T | G | 1 | a0001c0001t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-278-2573T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678208 | ||||||
chr8:70678369
|
T | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-278-2412T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678369 | ||||||
chr8:70678961
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-278-1820C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678961 | ||||||
chr8:70678968
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.-278-1813A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70678968 | ||||||
chr8:70679230
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-278-1551T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70679230 | ||||||
chr8:70679559
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-278-1222C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70679559 | ||||||
chr8:70680078
|
G | A | 112 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(109): Show | 120 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-278-703G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70680078 | ||||||
chr8:70680378
|
A | G | 1 | a0001c0002t0002g0283 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-278-403A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 2/4 | chr8 | 70680378 | ||||||
chr8:70681428
|
CTTA | C | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+101_272+103del others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70681428 | |||||
chr8:70681692
|
A | C | 1 | a0001c0002t0002g0227 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.272+362A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681692 | ||||||
chr8:70681787
|
TTAAGAAT others(20): Show |
T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+458_272+484del others(27): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681787 | ||||||
chr8:70681904
|
A | G | 2 | a0001c0001t0004g0167a0005c0009t0004g0166 | 2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.272+574A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681904 | ||||||
chr8:70681981
|
T | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+651T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70681981 | ||||||
chr8:70682089
|
T | C | 1 | a0001c0006t0007g0157 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.272+759T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682089 | ||||||
chr8:70682159
|
T | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+829T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682159 | ||||||
chr8:70682413
|
A | G | 1 | a0001c0002t0002g0165 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.272+1083A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682413 | ||||||
chr8:70682483
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+1153G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682483 | ||||||
chr8:70682670
|
CT | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+1342delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70682670 | |||||
chr8:70682812
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.272+1482A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682812 | ||||||
chr8:70682824
|
C | T | 118 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(115): Show | 126 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.272+1494C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682824 | ||||||
chr8:70682985
|
A | G | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+1655A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682985 | ||||||
chr8:70682991
|
C | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+1661C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70682991 | ||||||
chr8:70683168
|
T | C | 32 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(29): Show | 36 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.272+1838T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683168 | ||||||
chr8:70683247
|
T | A | 2 | a0001c0001t0004g0011a0001c0001t0004g0044 | 3 | HG02145.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.272+1917T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683247 | ||||||
chr8:70683300
|
A | G | 1 | a0001c0001t0003g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.272+1970A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683300 | ||||||
chr8:70683475
|
C | A | 1 | a0001c0001t0004g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.272+2145C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683475 | ||||||
chr8:70683544
|
G | A | 4 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+2214G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683544 | ||||||
chr8:70683729
|
C | T | 1 | a0001c0001t0004g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.272+2399C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683729 | ||||||
chr8:70683783
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.272+2453C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683783 | ||||||
chr8:70683803
|
T | G | 2 | a0001c0001t0007g0260a0001c0001t0018g0207 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.272+2473T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683803 | ||||||
chr8:70683805
|
C | T | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+2475C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683805 | ||||||
chr8:70683958
|
G | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+2628G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683958 | ||||||
chr8:70683989
|
T | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.272+2659T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70683989 | ||||||
chr8:70684021
|
T | G | 1 | a0001c0001t0020g0111 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.272+2691T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684021 | ||||||
chr8:70684142
|
A | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+2812A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684142 | ||||||
chr8:70684255
|
G | T | 8 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(5): Show | 8 | HG02071.hp2 NA18940.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.272+2925G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684255 | ||||||
chr8:70684298
|
C | G | 1 | a0001c0002t0002g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.272+2968C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684298 | ||||||
chr8:70684302
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.272+2972C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684302 | ||||||
chr8:70684363
|
T | C | 1 | a0001c0001t0004g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.272+3033T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684363 | ||||||
chr8:70684500
|
A | G | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+3170A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684500 | ||||||
chr8:70684573
|
GGTCT | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+3248_272+3251d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70684573 | |||||
chr8:70684652
|
A | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+3322A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684652 | ||||||
chr8:70684700
|
G | T | 196 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 213 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.272+3370G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684700 | ||||||
chr8:70684884
|
T | C | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+3554T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684884 | ||||||
chr8:70684894
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.272+3564C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684894 | ||||||
chr8:70684937
|
C | T | 1 | a0001c0001t0007g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.272+3607C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70684937 | ||||||
chr8:70685037
|
C | T | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+3707C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685037 | ||||||
chr8:70685038
|
G | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.272+3708G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685038 | ||||||
chr8:70685053
|
G | T | 105 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.272+3723G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685053 | ||||||
chr8:70685211
|
T | C | 1 | a0001c0002t0002g0212 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.272+3881T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685211 | ||||||
chr8:70685239
|
A | G | 4 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+3909A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685239 | ||||||
chr8:70685262
|
G | T | 1 | a0001c0003t0003g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.272+3932G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685262 | ||||||
chr8:70685276
|
G | A | 85 | a0001c0001t0001g0046a0001c0001t0001g0073a0001c0002t0002g0009others(82): Show | 94 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.272+3946G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685276 | ||||||
chr8:70685346
|
G | A | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.272+4016G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685346 | ||||||
chr8:70685359
|
G | C | 62 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(59): Show | 70 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.272+4029G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685359 | ||||||
chr8:70685408
|
A | C | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.272+4078A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685408 | ||||||
chr8:70685410
|
G | A | 1 | a0001c0006t0007g0157 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.272+4080G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685410 | ||||||
chr8:70685411
|
C | G | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.272+4081C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685411 | ||||||
chr8:70685412
|
A | G | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.272+4082A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685412 | ||||||
chr8:70685422
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.272+4092C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685422 | ||||||
chr8:70685490
|
T | TATA | 65 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(62): Show | 73 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.272+4180_272+4182d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | |||||
chr8:70685490
|
T | TATAATAA others(2): Show |
12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+4174_272+4182d others(11): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | |||||
chr8:70685490
|
T | TATAATAA others(8): Show |
1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.272+4168_272+4182d others(17): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | |||||
chr8:70685490
|
T | TATAATAA others(14): Show |
4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+4162_272+4182d others(23): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70685490 | |||||
chr8:70685635
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+4305C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685635 | ||||||
chr8:70685739
|
T | A | 4 | a0001c0001t0003g0129a0001c0001t0003g0130a0001c0001t0003g0135others(1): Show | 4 | HG01192.hp1 HG01255.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+4409T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685739 | ||||||
chr8:70685746
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.272+4416A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685746 | ||||||
chr8:70685749
|
G | A | 1 | a0001c0002t0002g0276 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.272+4419G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685749 | ||||||
chr8:70685752
|
G | A | 7 | a0001c0001t0004g0013a0001c0001t0004g0053a0001c0001t0004g0054others(4): Show | 8 | HG01243.hp2 HG01884.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.272+4422G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685752 | ||||||
chr8:70685769
|
G | T | 1 | a0001c0002t0002g0252 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.272+4439G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685769 | ||||||
chr8:70685786
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+4456A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685786 | ||||||
chr8:70685833
|
A | C | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+4503A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685833 | ||||||
chr8:70685957
|
T | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+4627T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70685957 | ||||||
chr8:70686003
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.272+4673A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686003 | ||||||
chr8:70686006
|
T | C | 1 | a0001c0002t0005g0237 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.272+4676T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686006 | ||||||
chr8:70686071
|
G | A | 1 | a0001c0001t0011g0176 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.272+4741G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686071 | ||||||
chr8:70686240
|
CT | C | 162 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(159): Show | 176 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.272+4926delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686240 | |||||
chr8:70686240
|
CTTTTTTT others(1): Show |
C | 16 | a0001c0002t0002g0023a0001c0002t0002g0027a0001c0002t0002g0165others(13): Show | 18 | HG02738.hp1 HG03942.hp1 HG04184.hp2 others(15): Show |
intron_variant | MODIFIER | c.272+4919_272+4926d others(10): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686240 | |||||
chr8:70686370
|
G | A | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.272+5040G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686370 | ||||||
chr8:70686407
|
T | G | 1 | a0001c0002t0002g0255 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.272+5077T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686407 | ||||||
chr8:70686412
|
AAT | A | 86 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(83): Show | 105 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.272+5101_272+5102d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686412 | |||||
chr8:70686412
|
AATAT | A | 82 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(79): Show | 91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+5099_272+5102d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70686412 | |||||
chr8:70686421
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0103 | 2 | HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.272+5091A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686421 | ||||||
chr8:70686472
|
C | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+5142C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686472 | ||||||
chr8:70686834
|
A | G | 1 | a0001c0001t0004g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.272+5504A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70686834 | ||||||
chr8:70687047
|
G | C | 1 | a0001c0001t0018g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.272+5717G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687047 | ||||||
chr8:70687088
|
T | TC | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+5761dupC | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687088 | |||||
chr8:70687179
|
C | G | 28 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(25): Show | 32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.272+5849C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687179 | ||||||
chr8:70687242
|
T | C | 1 | a0001c0001t0011g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.272+5912T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687242 | ||||||
chr8:70687293
|
G | T | 113 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(110): Show | 121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.272+5963G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687293 | ||||||
chr8:70687308
|
C | CTTCTCTT others(8): Show |
1 | a0001c0002t0002g0215 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.272+5979_272+5980i others(17): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687308 | |||||
chr8:70687310
|
C | T | 82 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(79): Show | 91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.272+5980C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687310 | ||||||
chr8:70687311
|
C | T | 1 | a0001c0002t0002g0215 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.272+5981C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687311 | ||||||
chr8:70687312
|
C | CTCTCTTT others(11): Show |
1 | a0001c0002t0002g0165 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.272+5985_272+5986i others(20): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
C | CTCTT | 55 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0068others(52): Show | 67 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.272+6026_272+6029d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
C | CTCTTTCT others(1): Show |
68 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0050others(65): Show | 79 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+6022_272+6029d others(10): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
C | CTCTTTCT others(5): Show |
49 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0047others(46): Show | 55 | HG00597.hp1 HG00639.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.272+6018_272+6029d others(14): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
C | CTCTTTCT others(9): Show |
24 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(21): Show | 25 | HG00597.hp2 HG01167.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.272+6014_272+6029d others(18): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
C | CTCTTTCT others(13): Show |
5 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0002t0002g0226others(2): Show | 5 | HG02735.hp1 HG03704.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+6010_272+6029d others(22): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
C | T | 1 | a0001c0002t0002g0215 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.272+5982C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687312 | ||||||
chr8:70687312
|
CTCTT | C | 12 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(9): Show | 12 | HG00140.hp2 HG01081.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.272+6026_272+6029d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
CTCTTTCT others(1): Show |
C | 7 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0004g0014others(4): Show | 8 | HG01978.hp2 HG02055.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.272+6022_272+6029d others(10): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
CTCTTTCT others(5): Show |
C | 12 | a0001c0001t0004g0032a0001c0001t0004g0034a0001c0001t0004g0035others(9): Show | 12 | HG00673.hp1 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.272+6018_272+6029d others(14): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687312
|
CTCTTTCT others(9): Show |
C | 24 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(21): Show | 28 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.272+6014_272+6029d others(18): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687312 | |||||
chr8:70687341
|
T | TCTTTCTT others(26): Show |
1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.272+6029_272+6030i others(35): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687341 | |||||
chr8:70687355
|
T | TTTCTTTC others(8): Show |
1 | a0001c0001t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.272+6029_272+6030i others(17): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687355 | |||||
chr8:70687358
|
C | CTTTCTTT others(3): Show |
1 | a0001c0003t0003g0156 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.272+6029_272+6030i others(12): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687358 | |||||
chr8:70687389
|
T | C | 232 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(229): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.272+6059T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687389 | ||||||
chr8:70687395
|
T | TTC | 113 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(110): Show | 121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.272+6080_272+6081d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70687395 | |||||
chr8:70687552
|
T | A | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+6222T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687552 | ||||||
chr8:70687817
|
T | G | 9 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0044others(6): Show | 11 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.272+6487T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687817 | ||||||
chr8:70687866
|
C | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+6536C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70687866 | ||||||
chr8:70688099
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.272+6769C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688099 | ||||||
chr8:70688239
|
G | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+6909G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688239 | ||||||
chr8:70688336
|
C | T | 1 | a0001c0001t0003g0145 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.272+7006C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688336 | ||||||
chr8:70688375
|
C | T | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+7045C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688375 | ||||||
chr8:70688437
|
G | A | 32 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(29): Show | 36 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.272+7107G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688437 | ||||||
chr8:70688618
|
A | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.272+7288A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688618 | ||||||
chr8:70688635
|
C | G | 1 | a0002c0004t0009g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.272+7305C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688635 | ||||||
chr8:70688707
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+7377T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688707 | ||||||
chr8:70688715
|
C | CT | 85 | a0001c0001t0001g0114a0001c0001t0001g0184a0001c0001t0004g0036others(82): Show | 94 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.272+7399dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70688715 | |||||
chr8:70688761
|
C | G | 67 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(64): Show | 75 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.272+7431C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688761 | ||||||
chr8:70688767
|
T | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.272+7437T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688767 | ||||||
chr8:70688916
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.272+7586C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70688916 | ||||||
chr8:70689017
|
C | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+7687C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689017 | ||||||
chr8:70689044
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.272+7714A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689044 | ||||||
chr8:70689047
|
C | T | 1 | a0001c0002t0002g0027 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.272+7717C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689047 | ||||||
chr8:70689306
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+7976T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689306 | ||||||
chr8:70689319
|
A | T | 17 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0022others(14): Show | 23 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.272+7989A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689319 | ||||||
chr8:70689341
|
A | G | 1 | a0001c0006t0007g0157 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.272+8011A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689341 | ||||||
chr8:70689443
|
AAT | A | 79 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(76): Show | 88 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.272+8128_272+8129d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70689443 | |||||
chr8:70689486
|
T | A | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+8156T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689486 | ||||||
chr8:70689499
|
TTA | T | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+8179_272+8180d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70689499 | |||||
chr8:70689513
|
A | G | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.272+8183A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689513 | ||||||
chr8:70689652
|
T | C | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+8322T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689652 | ||||||
chr8:70689681
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.272+8351C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689681 | ||||||
chr8:70689708
|
A | G | 4 | a0001c0002t0005g0237a0001c0002t0005g0239a0001c0002t0005g0240others(1): Show | 4 | HG01074.hp2 HG02004.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+8378A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689708 | ||||||
chr8:70689774
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+8444A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70689774 | ||||||
chr8:70690109
|
A | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+8779A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690109 | ||||||
chr8:70690159
|
A | C | 1 | a0001c0001t0017g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.272+8829A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690159 | ||||||
chr8:70690500
|
G | GT | 64 | a0001c0001t0001g0069a0001c0001t0001g0098a0001c0001t0001g0184others(61): Show | 71 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.272+9185dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70690500 | |||||
chr8:70690500
|
G | GTT | 14 | a0001c0002t0002g0243a0001c0002t0002g0244a0001c0002t0002g0256others(11): Show | 15 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.272+9184_272+9185d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70690500 | |||||
chr8:70690517
|
T | G | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+9187T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690517 | ||||||
chr8:70690602
|
G | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+9272G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690602 | ||||||
chr8:70690638
|
C | T | 1 | a0001c0002t0002g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.272+9308C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690638 | ||||||
chr8:70690679
|
A | G | 1 | a0001c0001t0010g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.272+9349A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690679 | ||||||
chr8:70690715
|
T | A | 4 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+9385T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690715 | ||||||
chr8:70690760
|
G | T | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.272+9430G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690760 | ||||||
chr8:70690844
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.272+9514G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690844 | ||||||
chr8:70690879
|
A | G | 2 | a0001c0006t0007g0007a0001c0006t0007g0157 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+9549A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690879 | ||||||
chr8:70690952
|
G | A | 1 | a0001c0001t0018g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.272+9622G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70690952 | ||||||
chr8:70691296
|
A | T | 1 | a0001c0001t0004g0035 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.272+9966A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691296 | ||||||
chr8:70691422
|
C | T | 1 | a0001c0002t0002g0027 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.272+10092C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691422 | ||||||
chr8:70691425
|
A | G | 1 | a0001c0002t0002g0165 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.272+10095A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691425 | ||||||
chr8:70691533
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.272+10203T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691533 | ||||||
chr8:70691646
|
C | G | 2 | a0001c0002t0002g0225a0001c0002t0002g0226 | 2 | NA19066.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.272+10316C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691646 | ||||||
chr8:70691710
|
G | A | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.272+10380G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691710 | ||||||
chr8:70691719
|
G | A | 2 | a0001c0001t0016g0045a0001c0001t0017g0030 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.272+10389G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691719 | ||||||
chr8:70691728
|
A | G | 1 | a0001c0001t0019g0181 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.272+10398A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691728 | ||||||
chr8:70691749
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+10419A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691749 | ||||||
chr8:70691903
|
T | G | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.272+10573T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691903 | ||||||
chr8:70691929
|
A | T | 1 | a0001c0001t0004g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.272+10599A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70691929 | ||||||
chr8:70692028
|
A | ATTC | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+10701_272+1070 others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70692028 | |||||
chr8:70692061
|
T | C | 2 | a0001c0002t0008g0208a0001c0002t0008g0209 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.272+10731T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692061 | ||||||
chr8:70692179
|
C | T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+10849C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692179 | ||||||
chr8:70692406
|
G | GT | 72 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(69): Show | 80 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.272+11085dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70692406 | |||||
chr8:70692470
|
A | G | 1 | a0003c0007t0001g0088 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.272+11140A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692470 | ||||||
chr8:70692577
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.272+11247T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692577 | ||||||
chr8:70692588
|
AT | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+11265delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70692588 | |||||
chr8:70692682
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.272+11352G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692682 | ||||||
chr8:70692768
|
C | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.272+11438C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692768 | ||||||
chr8:70692918
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0090 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.272+11588T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70692918 | ||||||
chr8:70693420
|
T | C | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.272+12090T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70693420 | ||||||
chr8:70693692
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+12362C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70693692 | ||||||
chr8:70693811
|
T | C | 1 | a0001c0002t0023g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.272+12481T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70693811 | ||||||
chr8:70693909
|
A | AGTT | 6 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.272+12581_272+1258 others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70693909 | |||||
chr8:70694000
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+12670G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694000 | ||||||
chr8:70694107
|
TC | T | 113 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(110): Show | 121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.272+12778delC | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694107 | ||||||
chr8:70694412
|
G | T | 1 | a0001c0003t0003g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.273-12521G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694412 | ||||||
chr8:70694430
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.273-12503G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694430 | ||||||
chr8:70694545
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0078 | 2 | NA18965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.273-12388C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694545 | ||||||
chr8:70694622
|
A | G | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.273-12311A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694622 | ||||||
chr8:70694651
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-12282C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694651 | ||||||
chr8:70694711
|
A | G | 1 | a0001c0002t0002g0270 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.273-12222A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694711 | ||||||
chr8:70694787
|
A | G | 285 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(282): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.273-12146A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694787 | ||||||
chr8:70694848
|
T | G | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-12085T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694848 | ||||||
chr8:70694927
|
A | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0178 | 2 | HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.273-12006A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70694927 | ||||||
chr8:70695002
|
G | T | 28 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(25): Show | 32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.273-11931G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695002 | ||||||
chr8:70695128
|
CT | C | 114 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(111): Show | 126 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.273-11788delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695128 | |||||
chr8:70695128
|
CTT | C | 7 | a0001c0001t0001g0123a0001c0002t0002g0219a0001c0002t0002g0248others(4): Show | 7 | HG01167.hp2 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.273-11789_273-1178 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695128 | |||||
chr8:70695128
|
CTTTTTTT | C | 24 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(21): Show | 25 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.273-11794_273-1178 others(11): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695128 | |||||
chr8:70695162
|
T | A | 1 | a0001c0003t0003g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.273-11771T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695162 | ||||||
chr8:70695163
|
A | T | 13 | a0001c0001t0004g0043a0001c0001t0004g0064a0001c0002t0005g0024others(10): Show | 14 | HG00642.hp1 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.273-11770A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695163 | ||||||
chr8:70695169
|
A | T | 2 | a0001c0006t0007g0007a0001c0006t0007g0157 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-11764A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695169 | ||||||
chr8:70695169
|
AT | A | 5 | a0001c0002t0002g0214a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-11755delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70695169 | |||||
chr8:70695170
|
T | A | 112 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(109): Show | 125 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.273-11763T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695170 | ||||||
chr8:70695174
|
T | A | 2 | a0001c0001t0001g0112a0002c0004t0002g0264 | 2 | HG01074.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.273-11759T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695174 | ||||||
chr8:70695259
|
A | G | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.273-11674A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695259 | ||||||
chr8:70695277
|
T | C | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-11656T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695277 | ||||||
chr8:70695327
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-11606C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695327 | ||||||
chr8:70695329
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-11604C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695329 | ||||||
chr8:70695332
|
G | C | 232 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(229): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.273-11601G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695332 | ||||||
chr8:70695354
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-11579A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695354 | ||||||
chr8:70695391
|
C | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-11542C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695391 | ||||||
chr8:70695432
|
G | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-11501G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695432 | ||||||
chr8:70695580
|
T | A | 1 | a0001c0001t0004g0041 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.273-11353T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695580 | ||||||
chr8:70695628
|
C | T | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-11305C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695628 | ||||||
chr8:70695639
|
C | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.273-11294C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695639 | ||||||
chr8:70695676
|
C | A | 1 | a0001c0002t0005g0239 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.273-11257C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695676 | ||||||
chr8:70695691
|
T | C | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273-11242T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695691 | ||||||
chr8:70695747
|
T | C | 84 | a0001c0001t0001g0072a0001c0002t0002g0009a0001c0002t0002g0010others(81): Show | 93 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.273-11186T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695747 | ||||||
chr8:70695768
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-11165G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695768 | ||||||
chr8:70695769
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-11164G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695769 | ||||||
chr8:70695784
|
A | G | 82 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(79): Show | 91 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.273-11149A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695784 | ||||||
chr8:70695788
|
C | A | 1 | a0001c0001t0012g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.273-11145C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695788 | ||||||
chr8:70695852
|
C | T | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.273-11081C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695852 | ||||||
chr8:70695901
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-11032T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695901 | ||||||
chr8:70695985
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.273-10948A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695985 | ||||||
chr8:70695993
|
T | C | 4 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-10940T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70695993 | ||||||
chr8:70696042
|
T | C | 1 | a0001c0001t0014g0134 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.273-10891T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696042 | ||||||
chr8:70696088
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.273-10845T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696088 | ||||||
chr8:70696093
|
G | C | 5 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-10840G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696093 | ||||||
chr8:70696109
|
A | T | 1 | a0001c0001t0003g0128 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.273-10824A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696109 | ||||||
chr8:70696215
|
C | T | 33 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(30): Show | 37 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.273-10718C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696215 | ||||||
chr8:70696317
|
C | T | 1 | a0001c0002t0023g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.273-10616C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696317 | ||||||
chr8:70696322
|
C | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10611C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696322 | ||||||
chr8:70696323
|
A | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10610A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696323 | ||||||
chr8:70696361
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-10572A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696361 | ||||||
chr8:70696436
|
G | C | 1 | a0001c0002t0002g0236 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.273-10497G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696436 | ||||||
chr8:70696497
|
A | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.273-10436A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696497 | ||||||
chr8:70696519
|
T | C | 4 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-10414T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696519 | ||||||
chr8:70696568
|
C | G | 2 | a0001c0006t0007g0007a0001c0006t0007g0157 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-10365C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696568 | ||||||
chr8:70696599
|
T | C | 1 | a0001c0002t0002g0280 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.273-10334T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696599 | ||||||
chr8:70696655
|
C | T | 1 | a0001c0001t0004g0032 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.273-10278C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696655 | ||||||
chr8:70696662
|
G | A | 232 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(229): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.273-10271G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696662 | ||||||
chr8:70696663
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10270C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696663 | ||||||
chr8:70696673
|
C | T | 280 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(277): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.273-10260C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696673 | ||||||
chr8:70696677
|
T | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-10256T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696677 | ||||||
chr8:70696699
|
GT | G | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-10228delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70696699 | |||||
chr8:70696832
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-10101G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696832 | ||||||
chr8:70696852
|
A | C | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.273-10081A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696852 | ||||||
chr8:70696899
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-10034A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696899 | ||||||
chr8:70696936
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-9997T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70696936 | ||||||
chr8:70697158
|
A | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-9775A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697158 | ||||||
chr8:70697159
|
G | A | 72 | a0001c0001t0001g0106a0001c0002t0002g0009a0001c0002t0002g0010others(69): Show | 80 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.273-9774G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697159 | ||||||
chr8:70697250
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.273-9683C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697250 | ||||||
chr8:70697323
|
T | C | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-9610T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697323 | ||||||
chr8:70697352
|
T | C | 1 | a0001c0002t0002g0227 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.273-9581T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697352 | ||||||
chr8:70697396
|
G | A | 1 | a0001c0001t0004g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273-9537G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697396 | ||||||
chr8:70697418
|
C | G | 1 | a0001c0001t0003g0127 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.273-9515C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697418 | ||||||
chr8:70697556
|
C | G | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-9377C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697556 | ||||||
chr8:70697667
|
C | A | 37 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(34): Show | 41 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.273-9266C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697667 | ||||||
chr8:70697774
|
T | C | 1 | a0001c0001t0004g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.273-9159T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697774 | ||||||
chr8:70697792
|
C | T | 70 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(67): Show | 78 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-9141C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697792 | ||||||
chr8:70697799
|
G | GA | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-9132dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70697799 | |||||
chr8:70697802
|
T | G | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-9131T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697802 | ||||||
chr8:70697830
|
G | A | 2 | a0001c0001t0004g0167a0005c0009t0004g0166 | 2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.273-9103G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697830 | ||||||
chr8:70697861
|
C | A | 5 | a0001c0001t0004g0038a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-9072C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697861 | ||||||
chr8:70697885
|
A | T | 1 | a0001c0001t0016g0045 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.273-9048A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697885 | ||||||
chr8:70697982
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.273-8951G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70697982 | ||||||
chr8:70698020
|
C | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-8913C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698020 | ||||||
chr8:70698020
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.273-8913C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698020 | ||||||
chr8:70698052
|
T | G | 2 | a0001c0001t0001g0172a0002c0004t0002g0264 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.273-8881T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698052 | ||||||
chr8:70698132
|
C | T | 4 | a0001c0001t0004g0012a0001c0001t0004g0033a0001c0001t0004g0041others(1): Show | 5 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-8801C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698132 | ||||||
chr8:70698194
|
C | G | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-8739C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698194 | ||||||
chr8:70698204
|
A | G | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-8729A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698204 | ||||||
chr8:70698365
|
A | C | 1 | a0001c0001t0003g0022 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.273-8568A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698365 | ||||||
chr8:70698542
|
C | T | 2 | a0001c0002t0002g0278a0001c0002t0002g0283 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.273-8391C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698542 | ||||||
chr8:70698545
|
A | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-8388A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698545 | ||||||
chr8:70698550
|
C | G | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273-8383C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698550 | ||||||
chr8:70698574
|
T | C | 28 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(25): Show | 32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.273-8359T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698574 | ||||||
chr8:70698663
|
T | C | 6 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(3): Show | 7 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.273-8270T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698663 | ||||||
chr8:70698702
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-8231C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698702 | ||||||
chr8:70698740
|
C | T | 2 | a0001c0001t0004g0013a0001c0001t0004g0057 | 3 | HG01884.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.273-8193C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698740 | ||||||
chr8:70698841
|
G | A | 118 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(115): Show | 131 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.273-8092G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698841 | ||||||
chr8:70698924
|
C | T | 6 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(3): Show | 7 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.273-8009C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698924 | ||||||
chr8:70698998
|
G | T | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-7935G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70698998 | ||||||
chr8:70699086
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-7847G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699086 | ||||||
chr8:70699182
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-7751G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699182 | ||||||
chr8:70699210
|
T | A | 3 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210 | 3 | HG02965.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.273-7723T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699210 | ||||||
chr8:70699453
|
T | G | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.273-7480T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699453 | ||||||
chr8:70699465
|
T | A | 283 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(280): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.273-7468T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699465 | ||||||
chr8:70699468
|
C | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-7465C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699468 | ||||||
chr8:70699561
|
C | T | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.273-7372C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699561 | ||||||
chr8:70699621
|
A | T | 1 | a0001c0002t0002g0235 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.273-7312A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699621 | ||||||
chr8:70699655
|
C | T | 14 | a0001c0001t0004g0064a0001c0002t0002g0222a0001c0002t0005g0024others(11): Show | 15 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.273-7278C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699655 | ||||||
chr8:70699678
|
G | A | 1 | a0001c0002t0002g0242 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.273-7255G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699678 | ||||||
chr8:70699792
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-7141C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699792 | ||||||
chr8:70699802
|
T | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-7131T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699802 | ||||||
chr8:70699822
|
A | G | 1 | a0001c0002t0002g0235 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.273-7111A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699822 | ||||||
chr8:70699942
|
A | G | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.273-6991A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70699942 | ||||||
chr8:70700049
|
C | A | 1 | a0001c0001t0003g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.273-6884C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700049 | ||||||
chr8:70700069
|
A | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-6864A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700069 | ||||||
chr8:70700166
|
C | A | 4 | a0001c0001t0004g0012a0001c0001t0004g0033a0001c0001t0004g0041others(1): Show | 5 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-6767C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700166 | ||||||
chr8:70700185
|
C | G | 4 | a0001c0001t0004g0014a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 5 | HG02055.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-6748C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700185 | ||||||
chr8:70700236
|
C | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-6697C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700236 | ||||||
chr8:70700300
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273-6633C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700300 | ||||||
chr8:70700300
|
CCT | C | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-6630_273-6629d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70700300 | |||||
chr8:70700478
|
C | T | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-6455C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700478 | ||||||
chr8:70700540
|
G | A | 2 | a0001c0001t0004g0054a0001c0001t0004g0055 | 2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.273-6393G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700540 | ||||||
chr8:70700637
|
GGGACCCA others(5): Show |
G | 2 | a0001c0001t0003g0020a0001c0001t0003g0133 | 3 | NA18944.hp1 NA18965.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.273-6292_273-6281d others(14): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70700637 | |||||
chr8:70700684
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-6249C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700684 | ||||||
chr8:70700781
|
T | C | 1 | a0001c0002t0002g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273-6152T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700781 | ||||||
chr8:70700844
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-6089T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700844 | ||||||
chr8:70700854
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-6079A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700854 | ||||||
chr8:70700866
|
T | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-6067T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700866 | ||||||
chr8:70700992
|
G | T | 1 | a0001c0001t0017g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.273-5941G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70700992 | ||||||
chr8:70701070
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.273-5863T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701070 | ||||||
chr8:70701157
|
G | A | 1 | a0001c0001t0003g0126 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.273-5776G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701157 | ||||||
chr8:70701201
|
C | T | 1 | a0001c0001t0004g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.273-5732C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701201 | ||||||
chr8:70701237
|
G | A | 86 | a0001c0001t0001g0079a0001c0001t0001g0090a0001c0001t0001g0099others(83): Show | 95 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.273-5696G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701237 | ||||||
chr8:70701276
|
C | T | 1 | a0001c0002t0002g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273-5657C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701276 | ||||||
chr8:70701277
|
G | A | 1 | a0001c0002t0002g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.273-5656G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701277 | ||||||
chr8:70701480
|
A | G | 8 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(5): Show | 8 | HG02071.hp2 NA18940.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.273-5453A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701480 | ||||||
chr8:70701574
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.273-5359G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701574 | ||||||
chr8:70701628
|
T | G | 1 | a0001c0002t0002g0216 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.273-5305T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701628 | ||||||
chr8:70701795
|
G | A | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-5138G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701795 | ||||||
chr8:70701808
|
A | G | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.273-5125A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70701808 | ||||||
chr8:70702012
|
C | T | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.273-4921C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702012 | ||||||
chr8:70702386
|
G | T | 1 | a0001c0002t0002g0221 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.273-4547G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702386 | ||||||
chr8:70702543
|
C | T | 30 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(27): Show | 33 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.273-4390C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702543 | ||||||
chr8:70702546
|
A | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-4387A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702546 | ||||||
chr8:70702896
|
A | G | 2 | a0001c0006t0007g0007a0001c0006t0007g0157 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-4037A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70702896 | ||||||
chr8:70703136
|
A | G | 1 | a0001c0002t0005g0024 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.273-3797A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703136 | ||||||
chr8:70703167
|
GT | G | 116 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(113): Show | 129 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(126): Show |
intron_variant | MODIFIER | c.273-3756delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70703167 | |||||
chr8:70703212
|
A | T | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-3721A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703212 | ||||||
chr8:70703318
|
T | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.273-3615T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703318 | ||||||
chr8:70703341
|
G | A | 1 | a0001c0001t0018g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273-3592G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703341 | ||||||
chr8:70703365
|
C | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-3568C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703365 | ||||||
chr8:70703481
|
G | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(103): Show | 114 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.273-3452G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703481 | ||||||
chr8:70703727
|
G | T | 89 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(86): Show | 108 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.273-3206G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703727 | ||||||
chr8:70703819
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.273-3114T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703819 | ||||||
chr8:70703876
|
T | C | 6 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG00673.hp2 NA18971.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.273-3057T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70703876 | ||||||
chr8:70704089
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.273-2844G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704089 | ||||||
chr8:70704107
|
G | A | 1 | a0001c0003t0003g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.273-2826G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704107 | ||||||
chr8:70704117
|
G | A | 1 | a0001c0001t0004g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273-2816G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704117 | ||||||
chr8:70704303
|
C | G | 4 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-2630C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704303 | ||||||
chr8:70704420
|
G | C | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.273-2513G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704420 | ||||||
chr8:70704448
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.273-2485T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704448 | ||||||
chr8:70704664
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.273-2269G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704664 | ||||||
chr8:70704694
|
A | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-2239A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704694 | ||||||
chr8:70704747
|
A | C | 172 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(169): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.273-2186A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704747 | ||||||
chr8:70704759
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0073others(5): Show | 9 | HG01175.hp1 HG02056.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-2174A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704759 | ||||||
chr8:70704810
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-2123G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704810 | ||||||
chr8:70704873
|
C | G | 1 | a0001c0001t0015g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.273-2060C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704873 | ||||||
chr8:70704961
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.273-1972A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70704961 | ||||||
chr8:70705181
|
A | G | 1 | a0001c0002t0002g0212 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.273-1752A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705181 | ||||||
chr8:70705203
|
ACTTCAGT others(17): Show |
A | 5 | a0001c0001t0004g0012a0001c0001t0004g0031a0001c0001t0004g0033others(2): Show | 6 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.273-1727_273-1704d others(26): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70705203 | |||||
chr8:70705447
|
A | G | 1 | a0001c0001t0018g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273-1486A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705447 | ||||||
chr8:70705480
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-1453A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705480 | ||||||
chr8:70705613
|
A | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-1320A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705613 | ||||||
chr8:70705685
|
G | T | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.273-1248G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705685 | ||||||
chr8:70705859
|
C | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.273-1074C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70705859 | ||||||
chr8:70706058
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.273-875A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706058 | ||||||
chr8:70706149
|
A | G | 1 | a0001c0001t0004g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273-784A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706149 | ||||||
chr8:70706223
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0178 | 2 | HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.273-710C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706223 | ||||||
chr8:70706239
|
C | T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-694C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706239 | ||||||
chr8:70706425
|
C | G | 36 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(33): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.273-508C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706425 | ||||||
chr8:70706532
|
T | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-401T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706532 | ||||||
chr8:70706635
|
C | A | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.273-298C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706635 | ||||||
chr8:70706739
|
A | G | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273-194A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | chr8 | 70706739 | ||||||
chr8:70706859
|
AATT | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.273-68_273-66delTA others(1): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 70706859 | |||||
chr8:70707550
|
T | C | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+397T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70707550 | ||||||
chr8:70707607
|
GGTT | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+458_493+460del others(3): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70707607 | |||||
chr8:70707723
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0109 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.493+570G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70707723 | ||||||
chr8:70707838
|
C | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+685C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70707838 | ||||||
chr8:70708023
|
T | C | 1 | a0001c0001t0004g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.493+870T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708023 | ||||||
chr8:70708052
|
C | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+899C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708052 | ||||||
chr8:70708287
|
A | G | 1 | a0001c0002t0005g0024 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.493+1134A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708287 | ||||||
chr8:70708363
|
A | G | 1 | a0001c0002t0008g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.493+1210A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708363 | ||||||
chr8:70708376
|
T | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | NA19002.hp1 NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.493+1223T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708376 | ||||||
chr8:70708423
|
C | T | 9 | a0001c0002t0002g0025a0001c0002t0002g0263a0001c0002t0002g0270others(6): Show | 10 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.493+1270C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708423 | ||||||
chr8:70708510
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.493+1357C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708510 | ||||||
chr8:70708546
|
A | G | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1393A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708546 | ||||||
chr8:70708561
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.493+1408C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708561 | ||||||
chr8:70708725
|
A | C | 1 | a0001c0001t0012g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.493+1572A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708725 | ||||||
chr8:70708838
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.493+1685C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708838 | ||||||
chr8:70708955
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+1802G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708955 | ||||||
chr8:70708966
|
A | G | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.493+1813A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70708966 | ||||||
chr8:70709033
|
G | T | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+1880G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709033 | ||||||
chr8:70709058
|
A | G | 1 | a0001c0001t0004g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.493+1905A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709058 | ||||||
chr8:70709481
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2328G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709481 | ||||||
chr8:70709617
|
A | T | 1 | a0001c0001t0003g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.493+2464A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709617 | ||||||
chr8:70709972
|
C | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2819C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709972 | ||||||
chr8:70709974
|
A | G | 4 | a0001c0001t0004g0012a0001c0001t0004g0033a0001c0001t0004g0041others(1): Show | 5 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+2821A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709974 | ||||||
chr8:70709991
|
T | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2838T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70709991 | ||||||
chr8:70710100
|
C | G | 51 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(48): Show | 64 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.493+2947C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710100 | ||||||
chr8:70710138
|
A | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+2985A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710138 | ||||||
chr8:70710156
|
T | C | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.493+3003T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710156 | ||||||
chr8:70710169
|
C | T | 28 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(25): Show | 32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.493+3016C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710169 | ||||||
chr8:70710273
|
C | T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+3120C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710273 | ||||||
chr8:70710293
|
A | G | 53 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(50): Show | 68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+3140A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710293 | ||||||
chr8:70710438
|
T | C | 172 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(169): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.493+3285T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710438 | ||||||
chr8:70710617
|
C | T | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+3464C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710617 | ||||||
chr8:70710618
|
G | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+3465G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710618 | ||||||
chr8:70710695
|
C | T | 2 | a0001c0001t0016g0045a0001c0001t0017g0030 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+3542C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710695 | ||||||
chr8:70710699
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.493+3546A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710699 | ||||||
chr8:70710702
|
TCAAACAA | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+3553_493+3559d others(9): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70710702 | |||||
chr8:70710704
|
AAAC | A | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+3569_493+3571d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70710704 | |||||
chr8:70710716
|
C | G | 2 | a0001c0001t0016g0045a0001c0001t0017g0030 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+3563C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710716 | ||||||
chr8:70710761
|
A | C | 2 | a0001c0001t0016g0045a0001c0001t0017g0030 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+3608A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710761 | ||||||
chr8:70710795
|
A | G | 1 | a0001c0001t0004g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.493+3642A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710795 | ||||||
chr8:70710820
|
G | T | 1 | a0001c0001t0017g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+3667G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710820 | ||||||
chr8:70710910
|
A | G | 3 | a0001c0002t0002g0255a0001c0002t0002g0265a0001c0002t0002g0266 | 3 | HG02630.hp1 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.493+3757A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710910 | ||||||
chr8:70710950
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.493+3797C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710950 | ||||||
chr8:70710951
|
G | A | 1 | a0001c0002t0002g0215 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.493+3798G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70710951 | ||||||
chr8:70711078
|
C | G | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+3925C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711078 | ||||||
chr8:70711130
|
T | C | 1 | a0001c0001t0004g0055 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.493+3977T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711130 | ||||||
chr8:70711152
|
G | A | 1 | a0001c0001t0004g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+3999G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711152 | ||||||
chr8:70711371
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.493+4218A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711371 | ||||||
chr8:70711532
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.493+4379C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711532 | ||||||
chr8:70711585
|
T | TAAACACA others(197): Show |
7 | a0001c0001t0004g0014a0001c0001t0004g0061a0001c0001t0004g0062others(4): Show | 8 | HG01167.hp1 HG02055.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.493+4640_493+4843d others(206): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711585 | |||||
chr8:70711585
|
TAAACACA others(197): Show |
T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+4640_493+4843d others(2): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711585 | |||||
chr8:70711605
|
A | ATAGACAT others(197): Show |
1 | a0001c0001t0017g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+4655_493+4656i others(206): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711605 | |||||
chr8:70711732
|
A | AATTTACC others(197): Show |
1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+4782_493+4783i others(206): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70711732 | |||||
chr8:70711809
|
A | G | 2 | a0001c0001t0016g0045a0001c0001t0017g0030 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.493+4656A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711809 | ||||||
chr8:70711924
|
C | T | 53 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(50): Show | 60 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.493+4771C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70711924 | ||||||
chr8:70712397
|
A | G | 51 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(48): Show | 64 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.493+5244A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712397 | ||||||
chr8:70712705
|
A | G | 1 | a0001c0001t0004g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.493+5552A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712705 | ||||||
chr8:70712765
|
A | G | 1 | a0001c0001t0016g0045 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.493+5612A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712765 | ||||||
chr8:70712986
|
C | T | 1 | a0001c0001t0017g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+5833C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70712986 | ||||||
chr8:70713001
|
A | G | 1 | a0001c0002t0002g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.493+5848A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713001 | ||||||
chr8:70713163
|
A | C | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.493+6010A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713163 | ||||||
chr8:70713268
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+6115G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713268 | ||||||
chr8:70713301
|
G | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+6148G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713301 | ||||||
chr8:70713353
|
T | A | 1 | a0001c0002t0002g0235 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.493+6200T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713353 | ||||||
chr8:70713453
|
G | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+6300G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713453 | ||||||
chr8:70713669
|
TAAG | T | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.493+6525_493+6527d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70713669 | |||||
chr8:70713712
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.493+6559C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713712 | ||||||
chr8:70713863
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+6710A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70713863 | ||||||
chr8:70714040
|
T | C | 180 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(177): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.493+6887T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714040 | ||||||
chr8:70714122
|
C | G | 1 | a0001c0003t0003g0141 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.493+6969C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714122 | ||||||
chr8:70714129
|
T | C | 273 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(270): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.493+6976T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714129 | ||||||
chr8:70714282
|
A | C | 6 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG00673.hp2 NA18971.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+7129A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714282 | ||||||
chr8:70714328
|
T | C | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+7175T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714328 | ||||||
chr8:70714428
|
A | G | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+7275A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714428 | ||||||
chr8:70714432
|
T | C | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.493+7279T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714432 | ||||||
chr8:70714449
|
CTGAT | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+7299_493+7302d others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70714449 | |||||
chr8:70714455
|
G | A | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+7302G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714455 | ||||||
chr8:70714475
|
T | C | 1 | a0001c0001t0017g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+7322T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714475 | ||||||
chr8:70714488
|
T | C | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+7335T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714488 | ||||||
chr8:70714537
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+7384G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714537 | ||||||
chr8:70714681
|
A | T | 1 | a0001c0002t0005g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.493+7528A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714681 | ||||||
chr8:70714717
|
G | A | 1 | a0001c0001t0007g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.493+7564G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714717 | ||||||
chr8:70714718
|
C | T | 13 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(10): Show | 14 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.493+7565C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714718 | ||||||
chr8:70714771
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.493+7618A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70714771 | ||||||
chr8:70715009
|
G | C | 1 | a0001c0002t0002g0257 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493+7856G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715009 | ||||||
chr8:70715209
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.493+8056A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715209 | ||||||
chr8:70715256
|
T | G | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+8103T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715256 | ||||||
chr8:70715270
|
A | G | 7 | a0001c0001t0004g0013a0001c0001t0004g0053a0001c0001t0004g0054others(4): Show | 8 | HG01243.hp2 HG01884.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+8117A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715270 | ||||||
chr8:70715372
|
A | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8219A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715372 | ||||||
chr8:70715420
|
A | G | 1 | a0001c0001t0014g0134 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.493+8267A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715420 | ||||||
chr8:70715487
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8334C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715487 | ||||||
chr8:70715510
|
G | T | 1 | a0001c0001t0007g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.493+8357G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715510 | ||||||
chr8:70715718
|
A | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+8565A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715718 | ||||||
chr8:70715744
|
A | C | 4 | a0001c0001t0011g0067a0001c0001t0011g0118a0001c0001t0011g0176others(1): Show | 4 | HG02132.hp1 HG02135.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+8591A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715744 | ||||||
chr8:70715777
|
A | C | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+8624A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715777 | ||||||
chr8:70715795
|
C | G | 53 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(50): Show | 68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+8642C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715795 | ||||||
chr8:70715833
|
G | T | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+8680G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715833 | ||||||
chr8:70715840
|
A | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+8687A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715840 | ||||||
chr8:70715851
|
A | C | 180 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(177): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.493+8698A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715851 | ||||||
chr8:70715861
|
G | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8708G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715861 | ||||||
chr8:70715976
|
A | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+8823A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70715976 | ||||||
chr8:70716064
|
A | G | 1 | a0002c0004t0009g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.493+8911A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716064 | ||||||
chr8:70716228
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+9075G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716228 | ||||||
chr8:70716335
|
G | A | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+9182G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716335 | ||||||
chr8:70716433
|
TG | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+9286delG | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70716433 | |||||
chr8:70716439
|
G | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+9286G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716439 | ||||||
chr8:70716445
|
G | A | 1 | a0001c0001t0004g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+9292G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716445 | ||||||
chr8:70716483
|
T | G | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+9330T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716483 | ||||||
chr8:70716518
|
G | A | 36 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(33): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.493+9365G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716518 | ||||||
chr8:70716708
|
C | A | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+9555C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716708 | ||||||
chr8:70716908
|
T | G | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+9755T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70716908 | ||||||
chr8:70716929
|
T | TA | 9 | a0001c0001t0001g0019a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 10 | HG02165.hp1 NA18612.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.493+9777dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70716929 | |||||
chr8:70717227
|
C | T | 1 | a0001c0001t0004g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+10074C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717227 | ||||||
chr8:70717241
|
CTG | C | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+10090_493+1009 others(6): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70717241 | |||||
chr8:70717257
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.493+10104C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717257 | ||||||
chr8:70717474
|
T | A | 4 | a0001c0001t0004g0034a0001c0001t0004g0039a0001c0001t0004g0040others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+10321T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717474 | ||||||
chr8:70717575
|
G | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+10422G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717575 | ||||||
chr8:70717720
|
C | G | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.493+10567C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717720 | ||||||
chr8:70717785
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.493+10632C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70717785 | ||||||
chr8:70718000
|
C | T | 1 | a0001c0002t0002g0212 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.493+10847C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718000 | ||||||
chr8:70718110
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.493+10957A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718110 | ||||||
chr8:70718119
|
A | G | 1 | a0001c0001t0004g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+10966A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718119 | ||||||
chr8:70718164
|
A | G | 53 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(50): Show | 68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+11011A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718164 | ||||||
chr8:70718192
|
A | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+11039A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718192 | ||||||
chr8:70718213
|
A | G | 1 | a0001c0002t0002g0025 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.493+11060A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718213 | ||||||
chr8:70718301
|
ATTAT | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+11159_493+1116 others(8): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70718301 | |||||
chr8:70718319
|
TTTTAC | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+11171_493+1117 others(9): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70718319 | |||||
chr8:70718552
|
A | G | 46 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(43): Show | 59 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.493+11399A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718552 | ||||||
chr8:70718669
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.493+11516G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718669 | ||||||
chr8:70718818
|
C | A | 1 | a0001c0002t0002g0222 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.493+11665C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718818 | ||||||
chr8:70718855
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.493+11702A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718855 | ||||||
chr8:70718873
|
T | C | 53 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(50): Show | 68 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.493+11720T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718873 | ||||||
chr8:70718896
|
C | T | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+11743C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718896 | ||||||
chr8:70718938
|
G | T | 1 | a0001c0001t0021g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.493+11785G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70718938 | ||||||
chr8:70719026
|
G | A | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.493+11873G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719026 | ||||||
chr8:70719160
|
T | G | 1 | a0001c0002t0002g0221 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.493+12007T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719160 | ||||||
chr8:70719246
|
C | T | 1 | a0001c0001t0015g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.493+12093C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719246 | ||||||
chr8:70719264
|
C | T | 1 | a0001c0002t0008g0241 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.493+12111C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719264 | ||||||
chr8:70719290
|
C | T | 1 | a0001c0001t0014g0134 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.493+12137C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719290 | ||||||
chr8:70719303
|
G | T | 1 | a0001c0002t0002g0276 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.493+12150G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719303 | ||||||
chr8:70719529
|
C | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.493+12376C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70719529 | ||||||
chr8:70720091
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+12938C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720091 | ||||||
chr8:70720116
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+12963G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720116 | ||||||
chr8:70720210
|
G | C | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+13057G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720210 | ||||||
chr8:70720282
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.493+13129C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720282 | ||||||
chr8:70720283
|
C | G | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+13130C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720283 | ||||||
chr8:70720283
|
C | T | 1 | a0001c0002t0002g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.493+13130C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720283 | ||||||
chr8:70720509
|
G | A | 1 | a0001c0001t0019g0181 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.494-13287G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720509 | ||||||
chr8:70720658
|
C | T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-13138C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720658 | ||||||
chr8:70720741
|
G | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-13055G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720741 | ||||||
chr8:70720989
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.494-12807G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70720989 | ||||||
chr8:70721022
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-12774G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721022 | ||||||
chr8:70721044
|
C | G | 28 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(25): Show | 32 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.494-12752C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721044 | ||||||
chr8:70721156
|
T | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-12640T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721156 | ||||||
chr8:70721219
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.494-12577G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721219 | ||||||
chr8:70721299
|
C | G | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-12497C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721299 | ||||||
chr8:70721313
|
C | G | 2 | a0001c0002t0002g0221a0001c0002t0002g0224 | 2 | NA18949.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.494-12483C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721313 | ||||||
chr8:70721543
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-12253T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721543 | ||||||
chr8:70721544
|
T | C | 4 | a0001c0002t0002g0222a0001c0002t0002g0247a0001c0002t0002g0280others(1): Show | 4 | HG00733.hp2 HG01255.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-12252T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721544 | ||||||
chr8:70721591
|
T | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-12205T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721591 | ||||||
chr8:70721607
|
C | T | 1 | a0001c0006t0007g0157 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.494-12189C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721607 | ||||||
chr8:70721610
|
T | C | 2 | a0001c0002t0002g0025a0001c0002t0002g0263 | 3 | HG02922.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.494-12186T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721610 | ||||||
chr8:70721650
|
C | A | 1 | a0001c0002t0002g0280 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.494-12146C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721650 | ||||||
chr8:70721721
|
A | G | 1 | a0001c0002t0022g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.494-12075A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721721 | ||||||
chr8:70721731
|
C | T | 1 | a0001c0001t0018g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.494-12065C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721731 | ||||||
chr8:70721732
|
G | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-12064G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721732 | ||||||
chr8:70721825
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.494-11971G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721825 | ||||||
chr8:70721938
|
C | T | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-11858C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721938 | ||||||
chr8:70721990
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.494-11806G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70721990 | ||||||
chr8:70722092
|
C | CT | 3 | a0001c0001t0003g0136a0003c0007t0001g0085a0003c0007t0001g0088 | 3 | NA19062.hp1 NA19062.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.494-11703dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70722092 | |||||
chr8:70722125
|
A | AT | 8 | a0001c0001t0003g0140a0001c0001t0003g0148a0001c0001t0003g0151others(5): Show | 8 | HG00621.hp1 HG02895.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-11659dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70722125 | |||||
chr8:70722223
|
A | C | 3 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274 | 3 | HG03209.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.494-11573A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722223 | ||||||
chr8:70722233
|
G | C | 4 | a0001c0001t0003g0022a0001c0001t0003g0137a0001c0001t0003g0138others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-11563G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722233 | ||||||
chr8:70722251
|
A | G | 1 | a0001c0001t0018g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.494-11545A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722251 | ||||||
chr8:70722411
|
G | A | 1 | a0001c0002t0022g0253 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.494-11385G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722411 | ||||||
chr8:70722704
|
C | T | 1 | a0001c0005t0006g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.494-11092C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722704 | ||||||
chr8:70722823
|
C | T | 4 | a0001c0001t0004g0043a0001c0001t0004g0064a0001c0001t0004g0167others(1): Show | 4 | HG01109.hp2 HG01167.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-10973C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722823 | ||||||
chr8:70722942
|
G | A | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-10854G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722942 | ||||||
chr8:70722995
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0125a0001c0001t0001g0177 | 3 | HG02074.hp1 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.494-10801C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70722995 | ||||||
chr8:70723436
|
G | A | 1 | a0001c0001t0004g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.494-10360G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723436 | ||||||
chr8:70723484
|
G | T | 9 | a0001c0002t0002g0025a0001c0002t0002g0263a0001c0002t0002g0270others(6): Show | 10 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-10312G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723484 | ||||||
chr8:70723564
|
C | G | 2 | a0001c0006t0007g0007a0001c0006t0007g0157 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-10232C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723564 | ||||||
chr8:70723566
|
G | C | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-10230G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723566 | ||||||
chr8:70723603
|
G | A | 1 | a0001c0002t0002g0268 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.494-10193G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723603 | ||||||
chr8:70723720
|
A | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-10076A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723720 | ||||||
chr8:70723766
|
C | A | 36 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(33): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-10030C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723766 | ||||||
chr8:70723766
|
C | T | 1 | a0001c0002t0002g0027 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.494-10030C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723766 | ||||||
chr8:70723772
|
C | T | 6 | a0001c0001t0004g0032a0001c0001t0004g0035a0001c0001t0004g0036others(3): Show | 6 | HG00673.hp1 HG01106.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.494-10024C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723772 | ||||||
chr8:70723793
|
C | T | 1 | a0001c0001t0004g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.494-10003C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723793 | ||||||
chr8:70723887
|
C | CT | 39 | a0001c0001t0001g0018a0001c0001t0001g0090a0001c0001t0001g0098others(36): Show | 44 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.494-9893dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70723887 | |||||
chr8:70723887
|
C | CTT | 66 | a0001c0001t0004g0167a0001c0002t0002g0009a0001c0002t0002g0010others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-9894_494-9893d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70723887 | |||||
chr8:70723887
|
C | CTTT | 17 | a0001c0002t0002g0229a0001c0002t0002g0258a0001c0002t0002g0283others(14): Show | 18 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.494-9895_494-9893d others(5): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70723887 | |||||
chr8:70723899
|
T | G | 1 | a0001c0001t0012g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494-9897T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723899 | ||||||
chr8:70723916
|
C | T | 5 | a0001c0001t0010g0203a0001c0001t0010g0204a0001c0001t0010g0205others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-9880C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723916 | ||||||
chr8:70723927
|
C | T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-9869C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723927 | ||||||
chr8:70723933
|
G | A | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.494-9863G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723933 | ||||||
chr8:70723952
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-9844G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723952 | ||||||
chr8:70723955
|
C | T | 1 | a0001c0002t0002g0214 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.494-9841C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723955 | ||||||
chr8:70723957
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.494-9839T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70723957 | ||||||
chr8:70724103
|
G | A | 36 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(33): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-9693G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724103 | ||||||
chr8:70724175
|
A | T | 1 | a0001c0001t0004g0040 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.494-9621A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724175 | ||||||
chr8:70724256
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.494-9540C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724256 | ||||||
chr8:70724430
|
G | GA | 109 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(106): Show | 128 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.494-9350dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | |||||
chr8:70724430
|
G | GAA | 9 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0083others(6): Show | 9 | HG00642.hp2 HG01081.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.494-9351_494-9350d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | |||||
chr8:70724430
|
GA | G | 94 | a0001c0001t0004g0012a0001c0001t0004g0013a0001c0001t0004g0014others(91): Show | 105 | HG00140.hp1 HG00140.hp2 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.494-9350delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | |||||
chr8:70724430
|
GAA | G | 16 | a0001c0002t0002g0257a0001c0002t0005g0024a0001c0002t0005g0237others(13): Show | 17 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.494-9351_494-9350d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70724430 | |||||
chr8:70724515
|
G | A | 2 | a0001c0006t0007g0007a0001c0006t0007g0157 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-9281G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724515 | ||||||
chr8:70724518
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.494-9278G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724518 | ||||||
chr8:70724528
|
A | T | 1 | a0001c0001t0004g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.494-9268A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724528 | ||||||
chr8:70724548
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.494-9248C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724548 | ||||||
chr8:70724554
|
G | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-9242G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724554 | ||||||
chr8:70724607
|
C | T | 1 | a0001c0002t0002g0216 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.494-9189C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724607 | ||||||
chr8:70724619
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.494-9177G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724619 | ||||||
chr8:70724781
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.494-9015G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724781 | ||||||
chr8:70724804
|
G | A | 1 | a0001c0002t0002g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.494-8992G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724804 | ||||||
chr8:70724913
|
T | G | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-8883T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724913 | ||||||
chr8:70724977
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-8819G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70724977 | ||||||
chr8:70725056
|
A | G | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-8740A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725056 | ||||||
chr8:70725245
|
G | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-8551G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725245 | ||||||
chr8:70725324
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-8472G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725324 | ||||||
chr8:70725378
|
C | T | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.494-8418C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725378 | ||||||
chr8:70725487
|
GA | G | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-8308delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725487 | ||||||
chr8:70725528
|
G | T | 8 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-8268G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725528 | ||||||
chr8:70725638
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.494-8158G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725638 | ||||||
chr8:70725669
|
G | C | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-8127G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725669 | ||||||
chr8:70725760
|
G | C | 1 | a0001c0001t0003g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.494-8036G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725760 | ||||||
chr8:70725773
|
G | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.494-8023G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725773 | ||||||
chr8:70725779
|
G | A | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-8017G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725779 | ||||||
chr8:70725947
|
A | T | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-7849A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70725947 | ||||||
chr8:70726085
|
G | A | 2 | a0001c0006t0007g0007a0001c0006t0007g0157 | 4 | HG02451.hp1 HG02615.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-7711G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726085 | ||||||
chr8:70726216
|
G | A | 1 | a0001c0001t0012g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494-7580G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726216 | ||||||
chr8:70726270
|
G | T | 1 | a0001c0002t0002g0027 | 2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.494-7526G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726270 | ||||||
chr8:70726310
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.494-7486C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726310 | ||||||
chr8:70726311
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.494-7485G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726311 | ||||||
chr8:70726595
|
C | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0175 | 2 | HG01515.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.494-7201C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726595 | ||||||
chr8:70726727
|
C | G | 1 | a0001c0001t0012g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494-7069C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726727 | ||||||
chr8:70726838
|
G | A | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-6958G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726838 | ||||||
chr8:70726948
|
C | T | 1 | a0001c0001t0011g0176 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.494-6848C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70726948 | ||||||
chr8:70726988
|
TA | T | 32 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(29): Show | 36 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.494-6801delA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70726988 | |||||
chr8:70727181
|
C | G | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-6615C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727181 | ||||||
chr8:70727207
|
C | G | 2 | a0001c0005t0006g0163a0001c0005t0006g0164 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.494-6589C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727207 | ||||||
chr8:70727277
|
T | A | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-6519T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727277 | ||||||
chr8:70727308
|
T | C | 1 | a0001c0002t0002g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.494-6488T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727308 | ||||||
chr8:70727317
|
A | T | 1 | a0001c0002t0002g0247 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.494-6479A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727317 | ||||||
chr8:70727327
|
G | GT | 21 | a0001c0001t0001g0019a0001c0001t0001g0070a0001c0001t0001g0108others(18): Show | 22 | HG00738.hp1 HG01891.hp2 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.494-6454dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70727327 | |||||
chr8:70727327
|
GT | G | 71 | a0001c0001t0001g0095a0001c0001t0003g0151a0001c0001t0004g0043others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.494-6454delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70727327 | |||||
chr8:70727327
|
GTT | G | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-6455_494-6454d others(4): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70727327 | |||||
chr8:70727463
|
C | T | 1 | a0001c0001t0011g0176 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.494-6333C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727463 | ||||||
chr8:70727469
|
T | A | 1 | a0001c0001t0003g0151 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494-6327T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727469 | ||||||
chr8:70727532
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-6264C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727532 | ||||||
chr8:70727572
|
T | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-6224T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727572 | ||||||
chr8:70727645
|
G | A | 2 | a0001c0001t0016g0045a0001c0001t0017g0030 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.494-6151G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727645 | ||||||
chr8:70727838
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.494-5958C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70727838 | ||||||
chr8:70728034
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-5762T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728034 | ||||||
chr8:70728067
|
G | A | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-5729G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728067 | ||||||
chr8:70728179
|
G | A | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-5617G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728179 | ||||||
chr8:70728260
|
C | T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-5536C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728260 | ||||||
chr8:70728333
|
A | G | 1 | a0001c0002t0002g0228 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.494-5463A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728333 | ||||||
chr8:70728453
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.494-5343A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728453 | ||||||
chr8:70728655
|
T | C | 1 | a0001c0001t0003g0151 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494-5141T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728655 | ||||||
chr8:70728664
|
A | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-5132A>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728664 | ||||||
chr8:70728893
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.494-4903G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728893 | ||||||
chr8:70728961
|
A | G | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.494-4835A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70728961 | ||||||
chr8:70729071
|
A | G | 1 | a0001c0002t0005g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.494-4725A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729071 | ||||||
chr8:70729237
|
G | A | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-4559G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729237 | ||||||
chr8:70729343
|
G | A | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-4453G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729343 | ||||||
chr8:70729408
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-4388T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729408 | ||||||
chr8:70729413
|
G | A | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.494-4383G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729413 | ||||||
chr8:70729415
|
TAGTTC | T | 4 | a0001c0001t0004g0034a0001c0001t0004g0039a0001c0001t0004g0040others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-4376_494-4372d others(7): Show |
XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70729415 | |||||
chr8:70729554
|
GT | G | 5 | a0002c0004t0002g0264a0002c0004t0009g0272a0002c0004t0009g0273others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-4238delT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70729554 | |||||
chr8:70729568
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.494-4228T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729568 | ||||||
chr8:70729585
|
A | C | 5 | a0001c0002t0002g0218a0001c0002t0002g0219a0001c0002t0002g0220others(2): Show | 5 | NA18940.hp1 NA18959.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-4211A>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729585 | ||||||
chr8:70729608
|
A | G | 1 | a0001c0002t0002g0243 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.494-4188A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729608 | ||||||
chr8:70729647
|
G | C | 1 | a0001c0001t0016g0045 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.494-4149G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729647 | ||||||
chr8:70729657
|
C | G | 1 | a0001c0002t0002g0218 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.494-4139C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729657 | ||||||
chr8:70729826
|
G | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-3970G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729826 | ||||||
chr8:70729915
|
A | G | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-3881A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729915 | ||||||
chr8:70729975
|
A | G | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-3821A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70729975 | ||||||
chr8:70730058
|
T | C | 1 | a0001c0002t0002g0255 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.494-3738T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730058 | ||||||
chr8:70730338
|
A | G | 119 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(116): Show | 132 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.494-3458A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730338 | ||||||
chr8:70730387
|
T | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.494-3409T>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730387 | ||||||
chr8:70730430
|
T | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0125a0001c0001t0001g0177 | 3 | HG02074.hp1 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.494-3366T>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730430 | ||||||
chr8:70730577
|
A | AT | 18 | a0001c0001t0017g0030a0001c0002t0005g0024a0001c0002t0005g0237others(15): Show | 19 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.494-3209dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70730577 | |||||
chr8:70730587
|
T | TA | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-3206dupA | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70730587 | |||||
chr8:70730612
|
G | A | 24 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(21): Show | 27 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.494-3184G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730612 | ||||||
chr8:70730665
|
G | A | 1 | a0001c0002t0002g0249 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.494-3131G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730665 | ||||||
chr8:70730713
|
G | T | 36 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(33): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-3083G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730713 | ||||||
chr8:70730774
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-3022T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730774 | ||||||
chr8:70730816
|
C | G | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-2980C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730816 | ||||||
chr8:70730888
|
G | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-2908G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70730888 | ||||||
chr8:70731107
|
C | T | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-2689C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731107 | ||||||
chr8:70731174
|
A | G | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-2622A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731174 | ||||||
chr8:70731185
|
C | A | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-2611C>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731185 | ||||||
chr8:70731324
|
C | CT | 83 | a0001c0001t0016g0045a0001c0002t0002g0009a0001c0002t0002g0010others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-2462dupT | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 70731324 | |||||
chr8:70731416
|
G | A | 1 | a0001c0002t0005g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.494-2380G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731416 | ||||||
chr8:70731562
|
C | T | 4 | a0001c0002t0008g0208a0001c0002t0008g0209a0001c0002t0008g0210others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-2234C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731562 | ||||||
chr8:70731666
|
G | T | 1 | a0005c0009t0004g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-2130G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731666 | ||||||
chr8:70731788
|
G | C | 12 | a0001c0002t0005g0024a0001c0002t0005g0237a0001c0002t0005g0238others(9): Show | 13 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-2008G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731788 | ||||||
chr8:70731809
|
T | C | 2 | a0001c0001t0004g0043a0001c0001t0004g0064 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.494-1987T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731809 | ||||||
chr8:70731872
|
C | T | 1 | a0001c0003t0003g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.494-1924C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70731872 | ||||||
chr8:70732016
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.494-1780G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732016 | ||||||
chr8:70732068
|
G | A | 1 | a0001c0002t0002g0280 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.494-1728G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732068 | ||||||
chr8:70732110
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.494-1686C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732110 | ||||||
chr8:70732221
|
A | G | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-1575A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732221 | ||||||
chr8:70732239
|
C | T | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.494-1557C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732239 | ||||||
chr8:70732301
|
A | G | 36 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(33): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-1495A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732301 | ||||||
chr8:70732493
|
C | T | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-1303C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732493 | ||||||
chr8:70732531
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.494-1265C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732531 | ||||||
chr8:70732572
|
T | C | 117 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(114): Show | 130 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(127): Show |
intron_variant | MODIFIER | c.494-1224T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732572 | ||||||
chr8:70732786
|
G | A | 1 | a0002c0004t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-1010G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732786 | ||||||
chr8:70732845
|
C | T | 4 | a0002c0004t0009g0272a0002c0004t0009g0273a0002c0004t0009g0274others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-951C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732845 | ||||||
chr8:70732921
|
C | G | 71 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(68): Show | 79 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.494-875C>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732921 | ||||||
chr8:70732937
|
G | A | 1 | a0001c0003t0003g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.494-859G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732937 | ||||||
chr8:70732968
|
G | A | 180 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003others(177): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.494-828G>A | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732968 | ||||||
chr8:70732982
|
G | C | 36 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0013others(33): Show | 40 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.494-814G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70732982 | ||||||
chr8:70733033
|
G | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-763G>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733033 | ||||||
chr8:70733119
|
A | G | 2 | a0001c0001t0013g0051a0001c0001t0013g0052 | 2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.494-677A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733119 | ||||||
chr8:70733389
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.494-407A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733389 | ||||||
chr8:70733418
|
G | T | 3 | a0001c0001t0011g0067a0001c0001t0011g0118a0001c0001t0011g0176 | 3 | HG02132.hp1 NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.494-378G>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733418 | ||||||
chr8:70733492
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.494-304A>G | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733492 | ||||||
chr8:70733625
|
T | C | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-171T>C | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733625 | ||||||
chr8:70733636
|
C | T | 83 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(80): Show | 92 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.494-160C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733636 | ||||||
chr8:70733691
|
C | T | 66 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(63): Show | 74 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-105C>T | XKR9 | ENSG00000221947.8 | transcript | ENST00000408926.8 | protein_coding | 4/4 | chr8 | 70733691 |