geneid | 23039 |
---|---|
ensemblid | ENSG00000130227.17 |
hgncid | 14108 |
symbol | XPO7 |
name | exportin 7 |
refseq_nuc | NM_015024.5 |
refseq_prot | NP_055839.3 |
ensembl_nuc | ENST00000252512.14 |
ensembl_prot | ENSP00000252512.9 |
mane_status | MANE Select |
chr | chr8 |
start | 21919662 |
end | 22006585 |
strand | + |
ver | v1.2 |
region | chr8:21919662-22006585 |
region5000 | chr8:21914662-22011585 |
regionname0 | XPO7_chr8_21919662_22006585 |
regionname5000 | XPO7_chr8_21914662_22011585 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1087 | 339 | 86 | 63 | 144 | 12 | 32 | 110 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0002 | 0/0 | 1087 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0003 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0004 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3264 | 116 | 18 | 28 | 54 | 2 | 13 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0002 | 0/0 | 3264 | 109 | 50 | 11 | 36 | 0 | 12 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0003 | 0/1 | 3264 | 86 | 14 | 16 | 45 | 4 | 6 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0004 | 0/0 | 3264 | 15 | 1 | 8 | 0 | 6 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0005 | 0/0 | 3264 | 4 | 1 | 0 | 2 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0006 | 0/0 | 3264 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0007 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0008 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0009 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0010 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0011 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0012 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
c0013 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1607 | 183 | 52 | 36 | 68 | 10 | 16 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0002 | 1/0 | 1607 | 126 | 19 | 28 | 62 | 2 | 14 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0003 | 0/0 | 1616 | 8 | 0 | 0 | 8 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0004 | 0/0 | 1608 | 7 | 2 | 0 | 5 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0005 | 0/0 | 1607 | 7 | 7 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0006 | 0/0 | 1607 | 3 | 3 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0007 | 0/0 | 1607 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0008 | 0/0 | 1607 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0009 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0010 | 0/0 | 1607 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0011 | 0/0 | 1607 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0012 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
t0013 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3264 | 116 | 18 | 28 | 54 | 2 | 13 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002 | 0/0 | 3264 | 109 | 50 | 11 | 36 | 0 | 12 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0003 | 0/1 | 3264 | 86 | 14 | 16 | 45 | 4 | 6 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0004 | 0/0 | 3264 | 15 | 1 | 8 | 0 | 6 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0005 | 0/0 | 3264 | 4 | 1 | 0 | 2 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0006 | 0/0 | 3264 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0007 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0008 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0009 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0010 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0002c0013 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0003c0012 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0004c0011 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 4870 | 113 | 17 | 28 | 53 | 2 | 12 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0001t0010 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0001t0011 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0001t0013 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0001 | 0/0 | 4870 | 88 | 37 | 11 | 30 | 0 | 10 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0002 | 0/0 | 4870 | 2 | 0 | 0 | 1 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0004 | 0/0 | 4871 | 7 | 2 | 0 | 5 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0005 | 0/0 | 4870 | 5 | 5 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0006 | 0/0 | 4870 | 3 | 3 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0007 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0008 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0002t0009 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0003t0001 | 0/1 | 4870 | 76 | 13 | 16 | 36 | 4 | 6 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0003t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0003t0003 | 0/0 | 4879 | 8 | 0 | 0 | 8 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0003t0012 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0004t0001 | 0/0 | 4870 | 15 | 1 | 8 | 0 | 6 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0005t0002 | 0/0 | 4870 | 4 | 1 | 0 | 2 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0006t0005 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0007t0001 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0008t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0009t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0001c0010t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0002c0013t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0003c0012t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
a0004c0011t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | copy fasta | chr8 | 21914662 | 22011585 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0001t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0007g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0008g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0002t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0003t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0004t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0005t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0006t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0006t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0007t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0007t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0008t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0008t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0009t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0009t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0001c0010t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0002c0013t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0003c0012t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
a0004c0011t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0004 | t0001 | g0301 | EUR | GBR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00323 | hp1 | a0001 | c0004 | t0001 | g0297 | EUR | FIN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0035 | EUR | FIN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0314 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00673 | hp2 | a0001 | c0007 | t0001 | g0310 | EAS | CHS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0109 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00738 | hp2 | a0001 | c0004 | t0001 | g0298 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0311 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0106 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0086 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0048 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0081 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01168 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0303 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0092 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0057 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0316 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0034 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01516 | hp1 | a0001 | c0004 | t0001 | g0313 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0088 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01517 | hp2 | a0001 | c0004 | t0001 | g0015 | EUR | IBS | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0307 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0302 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02055 | hp2 | a0001 | c0006 | t0005 | g0269 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0108 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CDX | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02280 | hp2 | a0001 | c0002 | t0007 | g0009 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02300 | hp1 | a0001 | c0004 | t0001 | g0304 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | PEL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02451 | hp1 | a0001 | c0004 | t0001 | g0305 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02572 | hp1 | a0001 | c0002 | t0005 | g0266 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02622 | hp1 | a0003 | c0012 | t0001 | g0251 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0281 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02809 | hp2 | a0001 | c0002 | t0009 | g0270 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02818 | hp2 | a0001 | c0002 | t0006 | g0318 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02895 | hp2 | a0001 | c0001 | t0013 | g0169 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0290 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02965 | hp2 | a0001 | c0002 | t0005 | g0261 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0089 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | GWD | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03139 | hp2 | a0001 | c0005 | t0002 | g0228 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03195 | hp1 | a0001 | c0002 | t0005 | g0265 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0066 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03453 | hp1 | a0001 | c0002 | t0006 | g0319 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03453 | hp2 | a0001 | c0002 | t0007 | g0009 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03486 | hp1 | a0001 | c0003 | t0012 | g0069 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0258 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0060 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0283 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0280 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0037 | SAS | PJL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0300 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0282 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0105 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0312 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04115 | hp1 | a0001 | c0002 | t0008 | g0271 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0285 | SAS | BEB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04199 | hp2 | a0001 | c0005 | t0002 | g0225 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0289 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04204 | hp2 | a0001 | c0001 | t0011 | g0247 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0272 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0306 | SAS | STU | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | CHB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18942 | hp1 | a0001 | c0003 | t0003 | g0104 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18947 | hp1 | a0001 | c0003 | t0001 | g0102 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18947 | hp2 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18950 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18957 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0096 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18961 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18965 | hp1 | a0001 | c0003 | t0003 | g0094 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18969 | hp2 | a0001 | c0003 | t0003 | g0070 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18970 | hp1 | a0001 | c0003 | t0003 | g0062 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18971 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18974 | hp2 | a0001 | c0003 | t0003 | g0113 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18975 | hp2 | a0001 | c0005 | t0002 | g0148 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18984 | hp1 | a0001 | c0009 | t0002 | g0077 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18985 | hp1 | a0001 | c0008 | t0002 | g0038 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18986 | hp2 | a0001 | c0003 | t0002 | g0295 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18988 | hp1 | a0001 | c0010 | t0002 | g0136 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18989 | hp2 | a0001 | c0007 | t0001 | g0315 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18990 | hp2 | a0001 | c0003 | t0003 | g0041 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18995 | hp2 | a0001 | c0003 | t0003 | g0073 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18997 | hp2 | a0001 | c0009 | t0002 | g0075 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19011 | hp2 | a0001 | c0008 | t0002 | g0059 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19030 | hp1 | a0001 | c0002 | t0005 | g0294 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19030 | hp2 | a0001 | c0002 | t0004 | g0291 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19076 | hp1 | a0001 | c0001 | t0010 | g0144 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19078 | hp1 | a0001 | c0005 | t0002 | g0153 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19085 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19089 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | YRI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20129 | hp1 | a0001 | c0002 | t0006 | g0320 | AFR | ASW | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ASW | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20752 | hp1 | a0001 | c0004 | t0001 | g0296 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0120 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0014 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0055 | EUR | TSI | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG01123 | hp2 | a0002 | c0013 | t0001 | g0091 | AMR | CLM | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG02559 | hp2 | a0001 | c0006 | t0005 | g0264 | AFR | ACB | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0068 | AFR | MSL | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
HG06807 | hp2 | a0004 | c0011 | t0002 | g0165 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | USA | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | LWK | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0032 | REF | REF | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0124 | REF | REF | XPO7_chr8_21914662_22011585 | XPO7 | chr8 | 21914662 | 22011585 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21989038
|
C | A | 1 | a0004 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1823C>A | p.Pro608Gln | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/28 | 1932/4870 | 1823/3264 | 608/1087 | chr8 | 21989038 | ||
chr8:21998827
|
A | G | 1 | a0003 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2418A>G | p.Ile806Met | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/28 | 2527/4870 | 2418/3264 | 806/1087 | chr8 | 21998827 | ||
chr8:22002221
|
G | C | 1 | a0002 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2892G>C | p.Glu964Asp | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/28 | 3001/4870 | 2892/3264 | 964/1087 | chr8 | 22002221 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21976454
|
C | T | 4 | a0001c0003a0001c0008a0001c0009others(1): Show | 91 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
synonymous_variant | LOW | c.696C>T | p.Ile232Ile | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/28 | 805/4870 | 696/3264 | 232/1087 | chr8 | 21976454 | ||
chr8:21980161
|
T | C | 1 | a0001c0010 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.915T>C | p.Ser305Ser | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/28 | 1024/4870 | 915/3264 | 305/1087 | chr8 | 21980161 | ||
chr8:21989075
|
G | C | 8 | a0001c0002a0001c0003a0001c0004others(5): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
synonymous_variant | LOW | c.1860G>C | p.Leu620Leu | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/28 | 1969/4870 | 1860/3264 | 620/1087 | chr8 | 21989075 | ||
chr8:21990344
|
G | C | 1 | a0001c0004 | 15 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(12): Show |
splice_region_variant&synonymous_variant | LOW | c.1869G>C | p.Gly623Gly | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/28 | 1978/4870 | 1869/3264 | 623/1087 | chr8 | 21990344 | ||
chr8:21990368
|
G | T | 1 | a0001c0006 | 2 | HG02055.hp2 HG02559.hp2 |
synonymous_variant | LOW | c.1893G>T | p.Val631Val | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/28 | 2002/4870 | 1893/3264 | 631/1087 | chr8 | 21990368 | ||
chr8:22005040
|
A | G | 7 | a0001c0002a0001c0003a0001c0004others(4): Show | 216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
synonymous_variant | LOW | c.3216A>G | p.Ser1072Ser | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 3325/4870 | 3216/3264 | 1072/1087 | chr8 | 22005040 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21919691
|
G | T | 2 | a0001c0002t0005a0001c0006t0005 | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-80G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 80 | chr8 | 21919691 | |||||
chr8:21919696
|
G | GGCGGCGG others(2): Show |
1 | a0001c0003t0003 | 8 | NA18942.hp1 NA18950.hp2 NA18965.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-69_-61dupGGCAGCGG others(1): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 60 | INFO_REALIGN_3_PRIME | chr8 | 21919696 | ||||
chr8:21919703
|
G | T | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-68G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 68 | chr8 | 21919703 | |||||
chr8:21919705
|
A | G | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 66 | chr8 | 21919705 | |||||
chr8:21919715
|
G | T | 1 | a0001c0003t0012 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/28 | 56 | chr8 | 21919715 | |||||
chr8:22005380
|
A | T | 1 | a0001c0002t0007 | 2 | HG02280.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 292 | chr8 | 22005380 | |||||
chr8:22005635
|
C | CA | 1 | a0001c0002t0004 | 7 | HG02922.hp2 NA18947.hp2 NA18957.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*556dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 557 | INFO_REALIGN_3_PRIME | chr8 | 22005635 | ||||
chr8:22005779
|
G | A | 15 | a0001c0002t0001a0001c0002t0004a0001c0002t0005others(12): Show | 213 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 691 | chr8 | 22005779 | |||||
chr8:22005929
|
G | A | 1 | a0001c0002t0008 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*841G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 841 | chr8 | 22005929 | |||||
chr8:22006035
|
T | G | 1 | a0001c0002t0006 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*947T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 947 | chr8 | 22006035 | |||||
chr8:22006219
|
T | A | 1 | a0001c0001t0010 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1131T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 1131 | chr8 | 22006219 | |||||
chr8:22006419
|
T | G | 1 | a0001c0001t0011 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 1331 | chr8 | 22006419 | |||||
chr8:22006495
|
C | T | 1 | a0001c0002t0009 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1407C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 28/28 | 1407 | chr8 | 22006495 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:21919805
|
G | A | 6 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(3): Show | 6 | HG00140.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+17G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919805 | ||||||
chr8:21919820
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.18+32C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919820 | ||||||
chr8:21919844
|
G | C | 8 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(5): Show | 9 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+56G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919844 | ||||||
chr8:21919874
|
G | A | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.18+86G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919874 | ||||||
chr8:21919965
|
G | A | 94 | a0001c0002t0001g0046a0001c0002t0001g0051a0001c0002t0001g0064others(91): Show | 99 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.18+177G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919965 | ||||||
chr8:21919967
|
C | T | 3 | a0001c0002t0001g0322a0001c0002t0001g0323a0001c0002t0001g0324 | 3 | HG00423.hp2 HG00621.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.18+179C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919967 | ||||||
chr8:21919972
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0122 | 3 | NA18959.hp1 NA18962.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.18+184G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21919972 | ||||||
chr8:21920084
|
C | G | 180 | a0001c0001t0002g0317a0001c0002t0001g0003a0001c0002t0001g0012others(177): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.18+296C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920084 | ||||||
chr8:21920109
|
C | T | 1 | a0001c0002t0001g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.18+321C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920109 | ||||||
chr8:21920237
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.18+449C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920237 | ||||||
chr8:21920280
|
C | T | 28 | a0001c0001t0002g0317a0001c0002t0001g0299a0001c0002t0001g0300others(25): Show | 30 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.18+492C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920280 | ||||||
chr8:21920454
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+666G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920454 | ||||||
chr8:21920571
|
T | C | 178 | a0001c0001t0002g0317a0001c0002t0001g0003a0001c0002t0001g0012others(175): Show | 188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.18+783T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920571 | ||||||
chr8:21920669
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.18+881C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920669 | ||||||
chr8:21920686
|
C | G | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+898C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21920686 | ||||||
chr8:21921100
|
T | G | 1 | a0001c0001t0002g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.18+1312T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921100 | ||||||
chr8:21921189
|
A | G | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+1401A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921189 | ||||||
chr8:21921204
|
G | C | 2 | a0001c0002t0001g0252a0003c0012t0001g0251 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.18+1416G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921204 | ||||||
chr8:21921206
|
A | G | 324 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(321): Show | 341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.18+1418A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921206 | ||||||
chr8:21921266
|
A | G | 1 | a0001c0001t0011g0247 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.18+1478A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921266 | ||||||
chr8:21921345
|
A | T | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+1557A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921345 | ||||||
chr8:21921562
|
T | C | 1 | a0001c0002t0005g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+1774T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921562 | ||||||
chr8:21921880
|
G | A | 1 | a0001c0002t0001g0006 | 2 | HG01257.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.18+2092G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921880 | ||||||
chr8:21921969
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+2181G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21921969 | ||||||
chr8:21922107
|
A | G | 1 | a0001c0002t0001g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.18+2319A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922107 | ||||||
chr8:21922162
|
C | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+2374C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922162 | ||||||
chr8:21922309
|
CTT | C | 23 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0306others(20): Show | 25 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+2523_18+2524del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21922309 | |||||
chr8:21922426
|
C | G | 74 | a0001c0001t0002g0243a0001c0002t0001g0006a0001c0002t0001g0229others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.18+2638C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922426 | ||||||
chr8:21922442
|
C | G | 23 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(20): Show | 23 | HG01433.hp1 HG02056.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+2654C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922442 | ||||||
chr8:21922466
|
C | T | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+2678C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922466 | ||||||
chr8:21922585
|
T | C | 20 | a0001c0002t0001g0126a0001c0002t0001g0272a0001c0002t0001g0273others(17): Show | 20 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+2797T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922585 | ||||||
chr8:21922686
|
C | T | 1 | a0001c0003t0012g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+2898C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922686 | ||||||
chr8:21922886
|
A | G | 20 | a0001c0002t0001g0126a0001c0002t0001g0272a0001c0002t0001g0273others(17): Show | 20 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+3098A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21922886 | ||||||
chr8:21923016
|
T | A | 2 | a0001c0002t0001g0253a0001c0002t0001g0254 | 2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.18+3228T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923016 | ||||||
chr8:21923221
|
C | G | 1 | a0001c0003t0001g0068 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+3433C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923221 | ||||||
chr8:21923233
|
A | G | 117 | a0001c0001t0002g0243a0001c0002t0001g0006a0001c0002t0001g0046others(114): Show | 123 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.18+3445A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923233 | ||||||
chr8:21923378
|
A | G | 1 | a0001c0002t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.18+3590A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923378 | ||||||
chr8:21923541
|
T | C | 1 | a0001c0002t0009g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+3753T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923541 | ||||||
chr8:21923872
|
A | G | 15 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276others(12): Show | 15 | HG02056.hp2 HG02738.hp2 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+4084A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21923872 | ||||||
chr8:21924118
|
C | T | 179 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(176): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+4330C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924118 | ||||||
chr8:21924355
|
T | C | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+4567T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924355 | ||||||
chr8:21924447
|
T | C | 1 | a0001c0002t0001g0229 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.18+4659T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924447 | ||||||
chr8:21924447
|
T | TC | 171 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0017others(168): Show | 178 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.18+4668dupC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21924447 | |||||
chr8:21924452
|
C | G | 1 | a0001c0002t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.18+4664C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924452 | ||||||
chr8:21924598
|
C | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+4810C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924598 | ||||||
chr8:21924651
|
G | A | 2 | a0001c0001t0002g0010a0001c0005t0002g0228 | 3 | HG00738.hp1 HG01099.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.18+4863G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924651 | ||||||
chr8:21924724
|
T | G | 4 | a0001c0002t0001g0229a0001c0002t0001g0230a0001c0002t0001g0239others(1): Show | 4 | HG02135.hp1 NA18940.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4936T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924724 | ||||||
chr8:21924788
|
C | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.18+5000C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924788 | ||||||
chr8:21924851
|
T | G | 1 | a0001c0002t0001g0229 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.18+5063T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924851 | ||||||
chr8:21924897
|
C | G | 5 | a0001c0002t0001g0275a0001c0002t0001g0276a0001c0002t0001g0277others(2): Show | 5 | NA18612.hp1 NA18968.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+5109C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21924897 | ||||||
chr8:21925052
|
G | A | 1 | a0001c0003t0001g0031 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.18+5264G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925052 | ||||||
chr8:21925120
|
A | G | 16 | a0001c0002t0001g0126a0001c0002t0001g0274a0001c0002t0001g0275others(13): Show | 16 | HG02056.hp2 HG02738.hp2 HG03688.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+5332A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925120 | ||||||
chr8:21925124
|
A | G | 3 | a0001c0002t0001g0293a0001c0006t0005g0264a0001c0006t0005g0269 | 3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.18+5336A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925124 | ||||||
chr8:21925169
|
A | G | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+5381A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925169 | ||||||
chr8:21925186
|
C | T | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+5398C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925186 | ||||||
chr8:21925386
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.18+5598A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925386 | ||||||
chr8:21925448
|
T | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+5660T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925448 | ||||||
chr8:21925626
|
T | C | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+5838T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925626 | ||||||
chr8:21925665
|
T | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+5877T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925665 | ||||||
chr8:21925681
|
G | C | 1 | a0001c0004t0001g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.18+5893G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925681 | ||||||
chr8:21925771
|
C | G | 1 | a0001c0001t0002g0170 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.18+5983C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925771 | ||||||
chr8:21925877
|
T | C | 1 | a0001c0001t0002g0127 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.18+6089T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925877 | ||||||
chr8:21925958
|
C | A | 1 | a0001c0002t0001g0257 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.18+6170C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21925958 | ||||||
chr8:21926357
|
G | A | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+6569G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21926357 | ||||||
chr8:21926555
|
GT | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0130others(12): Show | 16 | HG00673.hp1 HG01099.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+6777delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21926555 | |||||
chr8:21926627
|
CGTT | C | 77 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0011others(74): Show | 80 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.18+6842_18+6844del others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21926627 | |||||
chr8:21926693
|
A | G | 1 | a0001c0001t0002g0135 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.18+6905A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21926693 | ||||||
chr8:21926774
|
GA | G | 7 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(4): Show | 8 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+6994delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21926774 | |||||
chr8:21926897
|
C | T | 1 | a0001c0002t0001g0256 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.18+7109C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21926897 | ||||||
chr8:21927049
|
T | G | 86 | a0001c0001t0002g0162a0001c0002t0001g0003a0001c0002t0001g0012others(83): Show | 92 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.18+7261T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927049 | ||||||
chr8:21927139
|
C | CT | 4 | a0001c0002t0001g0272a0001c0002t0001g0273a0001c0002t0001g0289others(1): Show | 4 | HG01433.hp1 HG04115.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+7352dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927139 | |||||
chr8:21927141
|
G | T | 1 | a0001c0002t0001g0316 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.18+7353G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927141 | ||||||
chr8:21927224
|
TA | T | 118 | a0001c0001t0002g0227a0001c0001t0002g0243a0001c0002t0001g0006others(115): Show | 124 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.18+7444delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927224 | |||||
chr8:21927405
|
A | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+7617A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927405 | ||||||
chr8:21927478
|
A | G | 207 | a0001c0001t0002g0162a0001c0001t0002g0227a0001c0001t0002g0243others(204): Show | 219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.18+7690A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927478 | ||||||
chr8:21927505
|
G | A | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+7717G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927505 | ||||||
chr8:21927533
|
C | A | 1 | a0001c0002t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.18+7745C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927533 | ||||||
chr8:21927538
|
C | CT | 6 | a0001c0001t0002g0123a0001c0001t0002g0157a0001c0001t0002g0216others(3): Show | 6 | HG02040.hp2 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+7771dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927538 | |||||
chr8:21927538
|
CT | C | 86 | a0001c0001t0002g0130a0001c0001t0002g0162a0001c0002t0001g0003others(83): Show | 92 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.18+7771delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21927538 | |||||
chr8:21927558
|
T | C | 115 | a0001c0001t0002g0227a0001c0001t0002g0243a0001c0002t0001g0006others(112): Show | 121 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.18+7770T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927558 | ||||||
chr8:21927558
|
T | TC | 3 | a0001c0002t0001g0246a0001c0003t0001g0047a0001c0003t0001g0067 | 3 | HG02886.hp2 HG02965.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.18+7770_18+7771ins others(1): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927558 | ||||||
chr8:21927618
|
T | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+7830T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927618 | ||||||
chr8:21927725
|
A | C | 1 | a0001c0002t0001g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+7937A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927725 | ||||||
chr8:21927866
|
C | A | 4 | a0001c0002t0001g0306a0001c0002t0001g0307a0001c0002t0001g0308others(1): Show | 4 | HG01358.hp1 HG01928.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+8078C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927866 | ||||||
chr8:21927928
|
G | C | 3 | a0001c0002t0005g0258a0001c0002t0005g0265a0001c0002t0005g0294 | 3 | HG03195.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.18+8140G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21927928 | ||||||
chr8:21928070
|
A | T | 1 | a0001c0001t0002g0011 | 2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.18+8282A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928070 | ||||||
chr8:21928102
|
G | C | 1 | a0001c0002t0001g0309 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.18+8314G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928102 | ||||||
chr8:21928236
|
T | C | 7 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+8448T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928236 | ||||||
chr8:21928443
|
G | A | 1 | a0001c0003t0003g0070 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.18+8655G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928443 | ||||||
chr8:21928545
|
C | T | 1 | a0001c0002t0001g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.18+8757C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928545 | ||||||
chr8:21928787
|
G | A | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.18+8999G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928787 | ||||||
chr8:21928929
|
A | T | 45 | a0001c0001t0002g0162a0001c0002t0001g0003a0001c0002t0001g0022others(42): Show | 48 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.18+9141A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21928929 | ||||||
chr8:21929122
|
C | T | 3 | a0001c0002t0002g0250a0001c0002t0004g0290a0001c0002t0004g0291 | 3 | HG02922.hp2 NA18981.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+9334C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929122 | ||||||
chr8:21929130
|
C | G | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+9342C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929130 | ||||||
chr8:21929330
|
G | A | 1 | a0001c0002t0005g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+9542G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929330 | ||||||
chr8:21929478
|
C | T | 179 | a0001c0001t0002g0010a0001c0001t0002g0162a0001c0002t0001g0003others(176): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.18+9690C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929478 | ||||||
chr8:21929643
|
A | C | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+9855A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929643 | ||||||
chr8:21929668
|
A | G | 8 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+9880A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929668 | ||||||
chr8:21929802
|
A | C | 1 | a0001c0002t0001g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18+10014A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21929802 | ||||||
chr8:21930104
|
C | T | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+10316C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930104 | ||||||
chr8:21930212
|
G | T | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+10424G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930212 | ||||||
chr8:21930222
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+10434G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930222 | ||||||
chr8:21930242
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+10454T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930242 | ||||||
chr8:21930267
|
A | G | 4 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+10479A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930267 | ||||||
chr8:21930270
|
C | G | 1 | a0001c0005t0002g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.18+10482C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930270 | ||||||
chr8:21930271
|
C | T | 1 | a0001c0004t0001g0304 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.18+10483C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930271 | ||||||
chr8:21930388
|
A | G | 6 | a0001c0002t0005g0258a0001c0002t0005g0265a0001c0002t0005g0266others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+10600A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930388 | ||||||
chr8:21930755
|
G | A | 7 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+10967G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930755 | ||||||
chr8:21930858
|
A | T | 1 | a0001c0004t0001g0303 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.18+11070A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21930858 | ||||||
chr8:21931089
|
C | A | 27 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0306others(24): Show | 29 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.18+11301C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931089 | ||||||
chr8:21931168
|
C | CT | 22 | a0001c0002t0001g0126a0001c0002t0001g0272a0001c0002t0001g0273others(19): Show | 22 | HG01433.hp1 HG02004.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.18+11393dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21931168 | |||||
chr8:21931168
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.18+11380C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931168 | ||||||
chr8:21931214
|
G | A | 10 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(7): Show | 11 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+11426G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931214 | ||||||
chr8:21931308
|
G | A | 2 | a0001c0001t0002g0179a0001c0003t0001g0095 | 2 | HG01361.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.18+11520G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931308 | ||||||
chr8:21931354
|
G | C | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+11566G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931354 | ||||||
chr8:21931373
|
G | A | 1 | a0001c0003t0001g0032 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.18+11585G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931373 | ||||||
chr8:21931423
|
T | G | 179 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(176): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+11635T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931423 | ||||||
chr8:21931425
|
G | A | 94 | a0001c0002t0001g0046a0001c0002t0001g0051a0001c0002t0001g0064others(91): Show | 99 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.18+11637G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931425 | ||||||
chr8:21931473
|
C | T | 179 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(176): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+11685C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931473 | ||||||
chr8:21931846
|
A | T | 1 | a0001c0002t0001g0024 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.18+12058A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21931846 | ||||||
chr8:21932120
|
C | T | 5 | a0001c0002t0001g0257a0001c0002t0001g0260a0001c0002t0001g0262others(2): Show | 5 | HG02055.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+12332C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932120 | ||||||
chr8:21932593
|
G | GC | 4 | a0001c0001t0002g0171a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 4 | HG01256.hp1 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12806dupC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21932593 | |||||
chr8:21932646
|
T | TA | 51 | a0001c0003t0001g0071a0001c0003t0001g0072a0001c0003t0001g0074others(48): Show | 51 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.18+12862dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21932646 | |||||
chr8:21932729
|
A | G | 1 | a0001c0002t0001g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.18+12941A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932729 | ||||||
chr8:21932784
|
G | T | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+12996G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932784 | ||||||
chr8:21932925
|
A | G | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+13137A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932925 | ||||||
chr8:21932968
|
T | G | 27 | a0001c0002t0001g0051a0001c0002t0004g0001a0001c0002t0004g0049others(24): Show | 32 | HG00323.hp2 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.18+13180T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21932968 | ||||||
chr8:21933026
|
C | T | 3 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215 | 3 | NA19000.hp1 NA19005.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.18+13238C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933026 | ||||||
chr8:21933027
|
G | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG01934.hp2 HG02004.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.18+13239G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933027 | ||||||
chr8:21933096
|
A | AT | 17 | a0001c0001t0002g0010a0001c0001t0002g0021a0001c0001t0002g0129others(14): Show | 20 | HG00735.hp1 HG00738.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+13330dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21933096 | |||||
chr8:21933096
|
AT | A | 51 | a0001c0001t0002g0130a0001c0001t0002g0185a0001c0002t0001g0253others(48): Show | 53 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.18+13330delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21933096 | |||||
chr8:21933096
|
ATT | A | 107 | a0001c0002t0001g0046a0001c0002t0001g0051a0001c0002t0001g0064others(104): Show | 112 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.18+13329_18+13330d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21933096 | |||||
chr8:21933139
|
C | T | 14 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(11): Show | 15 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+13351C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933139 | ||||||
chr8:21933210
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.18+13422C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933210 | ||||||
chr8:21933286
|
G | C | 1 | a0001c0001t0002g0137 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.18+13498G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933286 | ||||||
chr8:21933601
|
C | G | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.18+13813C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933601 | ||||||
chr8:21933622
|
A | G | 1 | a0001c0004t0001g0301 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18+13834A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933622 | ||||||
chr8:21933625
|
T | G | 8 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(5): Show | 9 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+13837T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21933625 | ||||||
chr8:21934006
|
T | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0218 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.18+14218T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934006 | ||||||
chr8:21934021
|
C | T | 5 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+14233C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934021 | ||||||
chr8:21934046
|
C | T | 180 | a0001c0001t0002g0162a0001c0002t0001g0003a0001c0002t0001g0012others(177): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.18+14258C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934046 | ||||||
chr8:21934136
|
C | A | 3 | a0001c0003t0001g0071a0001c0003t0001g0096a0001c0003t0001g0097 | 3 | NA18953.hp2 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.18+14348C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934136 | ||||||
chr8:21934163
|
A | C | 1 | a0001c0002t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.18+14375A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934163 | ||||||
chr8:21934193
|
A | C | 1 | a0001c0002t0005g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+14405A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934193 | ||||||
chr8:21934261
|
C | T | 55 | a0001c0003t0001g0071a0001c0003t0001g0072a0001c0003t0001g0074others(52): Show | 55 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.18+14473C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934261 | ||||||
chr8:21934299
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.18+14511C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934299 | ||||||
chr8:21934415
|
C | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+14627C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934415 | ||||||
chr8:21934476
|
T | C | 1 | a0001c0003t0001g0031 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.18+14688T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934476 | ||||||
chr8:21934490
|
G | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+14702G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934490 | ||||||
chr8:21934656
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+14868G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934656 | ||||||
chr8:21934839
|
A | G | 7 | a0001c0002t0001g0257a0001c0002t0001g0259a0001c0002t0001g0260others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+15051A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934839 | ||||||
chr8:21934842
|
C | T | 2 | a0001c0001t0002g0208a0001c0002t0001g0155 | 2 | NA18985.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.18+15054C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934842 | ||||||
chr8:21934913
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+15125T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21934913 | ||||||
chr8:21935057
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.18+15269T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935057 | ||||||
chr8:21935070
|
T | C | 1 | a0001c0002t0001g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.18+15282T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935070 | ||||||
chr8:21935120
|
G | A | 3 | a0001c0002t0002g0250a0001c0002t0004g0290a0001c0002t0004g0291 | 3 | HG02922.hp2 NA18981.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+15332G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935120 | ||||||
chr8:21935455
|
ATTCTAGT others(154): Show |
A | 1 | a0001c0002t0001g0240 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.18+15670_18+15830d others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21935455 | |||||
chr8:21935468
|
G | A | 1 | a0001c0002t0005g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.18+15680G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935468 | ||||||
chr8:21935472
|
G | C | 179 | a0001c0001t0002g0162a0001c0002t0001g0003a0001c0002t0001g0012others(176): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+15684G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935472 | ||||||
chr8:21935822
|
T | TG | 183 | a0001c0001t0002g0010a0001c0001t0002g0162a0001c0002t0001g0003others(180): Show | 194 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.18+16037dupG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21935822 | |||||
chr8:21935838
|
C | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+16050C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935838 | ||||||
chr8:21935885
|
A | C | 1 | a0001c0002t0009g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+16097A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21935885 | ||||||
chr8:21936097
|
A | G | 84 | a0001c0001t0002g0162a0001c0002t0001g0003a0001c0002t0001g0012others(81): Show | 89 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.18+16309A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936097 | ||||||
chr8:21936115
|
G | A | 1 | a0001c0002t0001g0275 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.18+16327G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936115 | ||||||
chr8:21936117
|
C | G | 1 | a0001c0002t0009g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+16329C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936117 | ||||||
chr8:21936252
|
T | TTG | 3 | a0001c0002t0001g0293a0001c0006t0005g0264a0001c0006t0005g0269 | 3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.18+16467_18+16468d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21936252 | |||||
chr8:21936400
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.18+16612A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936400 | ||||||
chr8:21936421
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.18+16633G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936421 | ||||||
chr8:21936530
|
C | T | 180 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(177): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.18+16742C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936530 | ||||||
chr8:21936604
|
G | T | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.18+16816G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936604 | ||||||
chr8:21936619
|
A | G | 1 | a0001c0002t0001g0273 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.18+16831A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936619 | ||||||
chr8:21936676
|
T | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+16888T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936676 | ||||||
chr8:21936734
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.18+16946C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936734 | ||||||
chr8:21936768
|
C | T | 1 | a0001c0005t0002g0153 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.18+16980C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936768 | ||||||
chr8:21936868
|
T | C | 98 | a0001c0002t0001g0046a0001c0002t0001g0051a0001c0002t0001g0064others(95): Show | 103 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.18+17080T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21936868 | ||||||
chr8:21937097
|
A | C | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+17309A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937097 | ||||||
chr8:21937249
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.18+17461T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937249 | ||||||
chr8:21937323
|
G | T | 1 | a0001c0005t0002g0153 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.18+17535G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937323 | ||||||
chr8:21937363
|
C | T | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+17575C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937363 | ||||||
chr8:21937378
|
A | G | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.18+17590A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937378 | ||||||
chr8:21937437
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+17649G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937437 | ||||||
chr8:21937750
|
T | C | 2 | a0001c0002t0001g0253a0001c0002t0001g0254 | 2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.18+17962T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21937750 | ||||||
chr8:21938128
|
G | T | 1 | a0001c0003t0001g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.18+18340G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938128 | ||||||
chr8:21938496
|
A | G | 2 | a0001c0003t0001g0120a0002c0013t0001g0091 | 2 | HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.18+18708A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938496 | ||||||
chr8:21938575
|
G | A | 6 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(3): Show | 7 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+18787G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938575 | ||||||
chr8:21938779
|
A | T | 1 | a0001c0001t0002g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.18+18991A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938779 | ||||||
chr8:21938927
|
T | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+19139T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21938927 | ||||||
chr8:21939225
|
C | CT | 175 | a0001c0001t0002g0162a0001c0002t0001g0003a0001c0002t0001g0012others(172): Show | 185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.18+19450dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21939225 | |||||
chr8:21939493
|
T | C | 1 | a0001c0002t0001g0240 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.18+19705T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21939493 | ||||||
chr8:21939718
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.18+19930A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21939718 | ||||||
chr8:21940285
|
G | A | 5 | a0001c0002t0001g0275a0001c0002t0001g0276a0001c0002t0001g0277others(2): Show | 5 | NA18612.hp1 NA18968.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+20497G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940285 | ||||||
chr8:21940300
|
A | T | 1 | a0001c0003t0001g0071 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.18+20512A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940300 | ||||||
chr8:21940474
|
CT | C | 179 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(176): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+20699delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21940474 | |||||
chr8:21940523
|
G | C | 1 | a0001c0002t0005g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+20735G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940523 | ||||||
chr8:21940526
|
G | A | 1 | a0001c0002t0001g0013 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.18+20738G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940526 | ||||||
chr8:21940556
|
A | G | 1 | a0001c0003t0001g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.18+20768A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940556 | ||||||
chr8:21940805
|
C | T | 179 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(176): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+21017C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940805 | ||||||
chr8:21940918
|
C | T | 179 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(176): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+21130C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21940918 | ||||||
chr8:21941133
|
C | CT | 58 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(55): Show | 61 | HG00733.hp2 HG01433.hp1 HG01891.hp1 others(58): Show |
intron_variant | MODIFIER | c.18+21358dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21941133 | |||||
chr8:21941133
|
C | CTT | 94 | a0001c0002t0001g0046a0001c0002t0001g0051a0001c0002t0001g0064others(91): Show | 99 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.18+21357_18+21358d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21941133 | |||||
chr8:21941270
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.18+21482C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941270 | ||||||
chr8:21941364
|
C | A | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.18+21576C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941364 | ||||||
chr8:21941444
|
A | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | NA18949.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.18+21656A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941444 | ||||||
chr8:21941734
|
G | A | 84 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(81): Show | 89 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.18+21946G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941734 | ||||||
chr8:21941787
|
C | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0177 | 2 | HG00673.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.18+21999C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941787 | ||||||
chr8:21941838
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+22050G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941838 | ||||||
chr8:21941874
|
G | C | 2 | a0001c0003t0001g0048a0001c0003t0001g0057 | 2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.18+22086G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941874 | ||||||
chr8:21941903
|
A | G | 1 | a0001c0002t0001g0126 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.18+22115A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21941903 | ||||||
chr8:21942115
|
A | G | 94 | a0001c0002t0001g0046a0001c0002t0001g0051a0001c0002t0001g0064others(91): Show | 99 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.18+22327A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942115 | ||||||
chr8:21942182
|
A | G | 19 | a0001c0002t0001g0126a0001c0002t0001g0272a0001c0002t0001g0273others(16): Show | 19 | HG01433.hp1 HG02738.hp2 HG03688.hp1 others(16): Show |
intron_variant | MODIFIER | c.18+22394A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942182 | ||||||
chr8:21942226
|
C | A | 94 | a0001c0002t0001g0046a0001c0002t0001g0051a0001c0002t0001g0064others(91): Show | 99 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.18+22438C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942226 | ||||||
chr8:21942241
|
T | G | 7 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+22453T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942241 | ||||||
chr8:21942348
|
A | G | 7 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+22560A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942348 | ||||||
chr8:21942396
|
T | A | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+22608T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942396 | ||||||
chr8:21942398
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.18+22610A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942398 | ||||||
chr8:21942430
|
A | C | 24 | a0001c0001t0002g0162a0001c0002t0001g0299a0001c0002t0001g0300others(21): Show | 26 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.18+22642A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942430 | ||||||
chr8:21942594
|
G | A | 3 | a0001c0002t0001g0030a0001c0002t0001g0252a0003c0012t0001g0251 | 3 | HG02622.hp1 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.18+22806G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942594 | ||||||
chr8:21942796
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.18+23008G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942796 | ||||||
chr8:21942800
|
A | G | 1 | a0001c0010t0002g0136 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.18+23012A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942800 | ||||||
chr8:21942823
|
T | C | 1 | a0001c0005t0002g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.18+23035T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21942823 | ||||||
chr8:21943012
|
T | C | 1 | a0001c0002t0001g0159 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.18+23224T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943012 | ||||||
chr8:21943114
|
A | G | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+23326A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943114 | ||||||
chr8:21943229
|
A | G | 1 | a0001c0003t0001g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.18+23441A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943229 | ||||||
chr8:21943282
|
C | T | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+23494C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943282 | ||||||
chr8:21943289
|
T | C | 3 | a0001c0001t0002g0164a0001c0001t0002g0248a0001c0005t0002g0225 | 3 | HG02135.hp2 HG02155.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.18+23501T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943289 | ||||||
chr8:21943463
|
A | G | 1 | a0001c0002t0005g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-23394A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943463 | ||||||
chr8:21943522
|
G | C | 1 | a0001c0002t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-23335G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943522 | ||||||
chr8:21943580
|
C | T | 90 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(87): Show | 93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-23277C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943580 | ||||||
chr8:21943581
|
G | A | 8 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0001g0233others(5): Show | 8 | NA18949.hp2 NA18970.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-23276G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943581 | ||||||
chr8:21943630
|
G | A | 186 | a0001c0001t0002g0010a0001c0002t0001g0003a0001c0002t0001g0012others(183): Show | 198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.19-23227G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943630 | ||||||
chr8:21943684
|
T | C | 1 | a0001c0002t0001g0306 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.19-23173T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943684 | ||||||
chr8:21943970
|
C | T | 1 | a0001c0005t0002g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19-22887C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943970 | ||||||
chr8:21943997
|
C | G | 8 | a0001c0002t0001g0293a0001c0002t0005g0258a0001c0002t0005g0261others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-22860C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21943997 | ||||||
chr8:21944041
|
T | C | 20 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0130others(17): Show | 21 | HG00673.hp1 HG01099.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-22816T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944041 | ||||||
chr8:21944121
|
G | A | 1 | a0001c0001t0011g0247 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19-22736G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944121 | ||||||
chr8:21944223
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-22634C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944223 | ||||||
chr8:21944368
|
G | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-22489G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944368 | ||||||
chr8:21944456
|
A | C | 1 | a0001c0002t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-22401A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944456 | ||||||
chr8:21944485
|
T | G | 9 | a0001c0003t0001g0074a0001c0003t0001g0076a0001c0003t0001g0078others(6): Show | 9 | NA18747.hp1 NA18944.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-22372T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944485 | ||||||
chr8:21944607
|
C | T | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-22250C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944607 | ||||||
chr8:21944686
|
A | G | 184 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(181): Show | 195 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.19-22171A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944686 | ||||||
chr8:21944718
|
C | A | 3 | a0001c0003t0001g0079a0001c0003t0001g0080a0001c0003t0001g0102 | 3 | HG02165.hp1 NA18947.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.19-22139C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944718 | ||||||
chr8:21944729
|
G | A | 1 | a0001c0003t0001g0098 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.19-22128G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944729 | ||||||
chr8:21944761
|
C | T | 54 | a0001c0003t0001g0071a0001c0003t0001g0072a0001c0003t0001g0074others(51): Show | 54 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.19-22096C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944761 | ||||||
chr8:21944765
|
T | G | 90 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(87): Show | 93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-22092T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944765 | ||||||
chr8:21944779
|
G | A | 90 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(87): Show | 93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-22078G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944779 | ||||||
chr8:21944854
|
T | A | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-22003T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944854 | ||||||
chr8:21944921
|
G | A | 94 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(91): Show | 102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.19-21936G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21944921 | ||||||
chr8:21945063
|
C | T | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-21794C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945063 | ||||||
chr8:21945088
|
C | T | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-21769C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945088 | ||||||
chr8:21945147
|
C | T | 1 | a0001c0003t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19-21710C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945147 | ||||||
chr8:21945150
|
G | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-21707G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945150 | ||||||
chr8:21945175
|
C | T | 3 | a0001c0003t0001g0032a0001c0003t0001g0060a0001c0003t0001g0061 | 3 | HG01167.hp2 HG03654.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.19-21682C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945175 | ||||||
chr8:21945211
|
A | C | 1 | a0001c0001t0002g0227 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.19-21646A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945211 | ||||||
chr8:21945326
|
A | G | 94 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(91): Show | 102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.19-21531A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945326 | ||||||
chr8:21945349
|
TAGAC | T | 54 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(51): Show | 60 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.19-21504_19-21501d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21945349 | |||||
chr8:21945399
|
A | T | 91 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(88): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-21458A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945399 | ||||||
chr8:21945497
|
A | G | 185 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(182): Show | 196 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.19-21360A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945497 | ||||||
chr8:21945545
|
A | T | 1 | a0001c0001t0002g0010 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.19-21312A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945545 | ||||||
chr8:21945580
|
A | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-21277A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945580 | ||||||
chr8:21945814
|
A | G | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0001c0002t0001g0239 | 3 | NA18940.hp2 NA18950.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.19-21043A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945814 | ||||||
chr8:21945891
|
G | A | 1 | a0001c0002t0005g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-20966G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945891 | ||||||
chr8:21945923
|
G | A | 3 | a0001c0002t0006g0318a0001c0002t0006g0319a0001c0002t0006g0320 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.19-20934G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21945923 | ||||||
chr8:21946214
|
C | T | 24 | a0001c0002t0001g0051a0001c0002t0001g0126a0001c0002t0001g0272others(21): Show | 26 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-20643C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946214 | ||||||
chr8:21946224
|
C | A | 92 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(89): Show | 100 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.19-20633C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946224 | ||||||
chr8:21946305
|
A | C | 91 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(88): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-20552A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946305 | ||||||
chr8:21946368
|
T | A | 2 | a0001c0003t0001g0004a0001c0003t0001g0052 | 3 | HG01891.hp2 HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.19-20489T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946368 | ||||||
chr8:21946475
|
C | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-20382C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946475 | ||||||
chr8:21946575
|
A | G | 1 | a0001c0001t0002g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19-20282A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946575 | ||||||
chr8:21946580
|
A | AC | 92 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(89): Show | 100 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.19-20277_19-20276i others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946580 | ||||||
chr8:21946585
|
A | AAAC | 52 | a0001c0002t0004g0290a0001c0002t0004g0291a0001c0003t0001g0056others(49): Show | 52 | HG00558.hp1 HG00735.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.19-20272_19-20271i others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946585 | ||||||
chr8:21946585
|
A | AAACAAAA others(10): Show |
1 | a0001c0003t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.19-20272_19-20271i others(19): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946585 | ||||||
chr8:21946585
|
A | AAC | 35 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(32): Show | 38 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.19-20272_19-20271i others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946585 | ||||||
chr8:21946586
|
C | A | 93 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(90): Show | 96 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.19-20271C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946586 | ||||||
chr8:21946586
|
C | CA | 110 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0243others(107): Show | 119 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.19-20259dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21946586 | |||||
chr8:21946591
|
A | AC | 4 | a0001c0002t0005g0258a0001c0002t0005g0265a0001c0002t0005g0294others(1): Show | 4 | HG02622.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-20266_19-20265i others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946591 | ||||||
chr8:21946640
|
A | AT | 75 | a0001c0001t0002g0127a0001c0001t0002g0151a0001c0001t0002g0152others(72): Show | 81 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-20196dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21946640 | |||||
chr8:21946640
|
A | ATT | 9 | a0001c0002t0001g0254a0001c0002t0001g0260a0001c0002t0001g0268others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-20197_19-20196d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21946640 | |||||
chr8:21946644
|
T | G | 3 | a0001c0002t0001g0293a0001c0006t0005g0264a0001c0006t0005g0269 | 3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-20213T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946644 | ||||||
chr8:21946807
|
T | TTA | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-20050_19-20049i others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21946807 | ||||||
chr8:21947172
|
A | G | 1 | a0001c0002t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19-19685A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947172 | ||||||
chr8:21947474
|
G | A | 2 | a0001c0007t0001g0310a0001c0007t0001g0315 | 2 | HG00673.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.19-19383G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947474 | ||||||
chr8:21947478
|
A | G | 91 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(88): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-19379A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947478 | ||||||
chr8:21947521
|
A | G | 1 | a0001c0001t0002g0201 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.19-19336A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947521 | ||||||
chr8:21947560
|
A | G | 1 | a0001c0002t0001g0051 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.19-19297A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947560 | ||||||
chr8:21947754
|
T | C | 94 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(91): Show | 102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.19-19103T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947754 | ||||||
chr8:21947924
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19-18933C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947924 | ||||||
chr8:21947996
|
G | C | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-18861G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21947996 | ||||||
chr8:21948109
|
C | G | 24 | a0001c0001t0002g0162a0001c0002t0001g0299a0001c0002t0001g0300others(21): Show | 26 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.19-18748C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948109 | ||||||
chr8:21948212
|
G | T | 1 | a0001c0002t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-18645G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948212 | ||||||
chr8:21948420
|
C | A | 1 | a0001c0001t0002g0204 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.19-18437C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948420 | ||||||
chr8:21948467
|
G | A | 1 | a0001c0002t0001g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.19-18390G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948467 | ||||||
chr8:21948546
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.19-18311C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948546 | ||||||
chr8:21948584
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.19-18273A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948584 | ||||||
chr8:21948652
|
A | G | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-18205A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948652 | ||||||
chr8:21948671
|
G | A | 1 | a0001c0002t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19-18186G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948671 | ||||||
chr8:21948737
|
G | A | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-18120G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21948737 | ||||||
chr8:21949012
|
C | T | 1 | a0001c0002t0001g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.19-17845C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949012 | ||||||
chr8:21949030
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-17827A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949030 | ||||||
chr8:21949041
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.19-17816G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949041 | ||||||
chr8:21949157
|
C | A | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-17700C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949157 | ||||||
chr8:21949265
|
T | C | 1 | a0001c0003t0002g0295 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-17592T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949265 | ||||||
chr8:21949278
|
G | A | 2 | a0001c0001t0002g0010a0001c0005t0002g0228 | 3 | HG00738.hp1 HG01099.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-17579G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949278 | ||||||
chr8:21949292
|
G | A | 27 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0306others(24): Show | 29 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-17565G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949292 | ||||||
chr8:21949541
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.19-17316G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21949541 | ||||||
chr8:21949714
|
CTGTT | C | 91 | a0001c0001t0002g0182a0001c0002t0001g0046a0001c0002t0001g0064others(88): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-17138_19-17135d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21949714 | |||||
chr8:21950069
|
C | A | 1 | a0001c0002t0009g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-16788C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950069 | ||||||
chr8:21950106
|
T | C | 1 | a0001c0001t0002g0005 | 2 | NA18959.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.19-16751T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950106 | ||||||
chr8:21950210
|
G | A | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19-16647G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950210 | ||||||
chr8:21950242
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.19-16615G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950242 | ||||||
chr8:21950246
|
A | G | 77 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.19-16611A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950246 | ||||||
chr8:21950888
|
G | C | 1 | a0001c0002t0001g0257 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.19-15969G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950888 | ||||||
chr8:21950927
|
G | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-15930G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950927 | ||||||
chr8:21950959
|
A | C | 1 | a0003c0012t0001g0251 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19-15898A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21950959 | ||||||
chr8:21951090
|
T | TTTAA | 3 | a0001c0002t0001g0022a0001c0002t0001g0028a0001c0003t0001g0089 | 3 | HG02976.hp2 HG03017.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.19-15742_19-15739d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21951090 | |||||
chr8:21951205
|
C | T | 8 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-15652C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951205 | ||||||
chr8:21951229
|
A | G | 1 | a0002c0013t0001g0091 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-15628A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951229 | ||||||
chr8:21951263
|
G | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-15594G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951263 | ||||||
chr8:21951334
|
A | G | 7 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 8 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-15523A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951334 | ||||||
chr8:21951462
|
A | G | 3 | a0001c0001t0002g0150a0001c0001t0002g0199a0001c0001t0002g0200 | 3 | HG00621.hp1 NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.19-15395A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951462 | ||||||
chr8:21951504
|
A | G | 34 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(31): Show | 37 | HG01433.hp1 HG01891.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.19-15353A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951504 | ||||||
chr8:21951587
|
C | G | 3 | a0001c0003t0001g0048a0001c0003t0001g0056a0001c0003t0001g0057 | 3 | HG01109.hp1 HG01261.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.19-15270C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951587 | ||||||
chr8:21951662
|
T | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0020 | 3 | HG00140.hp2 HG01433.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.19-15195T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951662 | ||||||
chr8:21951829
|
A | AT | 113 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(110): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.19-15027dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21951829 | |||||
chr8:21951908
|
G | T | 1 | a0001c0001t0002g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.19-14949G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21951908 | ||||||
chr8:21952074
|
T | G | 7 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-14783T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952074 | ||||||
chr8:21952226
|
T | C | 2 | a0001c0002t0001g0272a0001c0002t0001g0289 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.19-14631T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952226 | ||||||
chr8:21952248
|
G | T | 2 | a0001c0002t0001g0012a0001c0002t0001g0013 | 4 | HG02109.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-14609G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952248 | ||||||
chr8:21952486
|
C | G | 3 | a0001c0001t0002g0164a0001c0001t0002g0248a0001c0005t0002g0225 | 3 | HG02135.hp2 HG02155.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.19-14371C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952486 | ||||||
chr8:21952582
|
T | G | 2 | a0001c0006t0005g0264a0001c0006t0005g0269 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-14275T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952582 | ||||||
chr8:21952689
|
C | T | 1 | a0001c0003t0001g0031 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19-14168C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952689 | ||||||
chr8:21952836
|
G | C | 1 | a0001c0001t0002g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.19-14021G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952836 | ||||||
chr8:21952866
|
C | T | 182 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(179): Show | 193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.19-13991C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952866 | ||||||
chr8:21952883
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19-13974G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952883 | ||||||
chr8:21952997
|
A | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0202 | 2 | HG01175.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19-13860A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21952997 | ||||||
chr8:21953092
|
G | A | 92 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(89): Show | 100 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.19-13765G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953092 | ||||||
chr8:21953113
|
C | T | 3 | a0001c0003t0001g0032a0001c0003t0001g0060a0001c0003t0001g0061 | 3 | HG01167.hp2 HG03654.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.19-13744C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953113 | ||||||
chr8:21953129
|
G | T | 2 | a0001c0005t0002g0148a0001c0005t0002g0153 | 2 | NA18975.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.19-13728G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953129 | ||||||
chr8:21953282
|
C | G | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-13575C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953282 | ||||||
chr8:21953542
|
G | A | 1 | a0001c0003t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19-13315G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953542 | ||||||
chr8:21953644
|
C | T | 1 | a0001c0002t0007g0009 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19-13213C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953644 | ||||||
chr8:21953713
|
T | G | 1 | a0001c0003t0012g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.19-13144T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953713 | ||||||
chr8:21953778
|
T | C | 1 | a0001c0001t0002g0130 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.19-13079T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953778 | ||||||
chr8:21953785
|
G | C | 1 | a0001c0005t0002g0225 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19-13072G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953785 | ||||||
chr8:21953844
|
T | A | 1 | a0001c0002t0001g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.19-13013T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21953844 | ||||||
chr8:21954019
|
C | G | 112 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(109): Show | 116 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-12838C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954019 | ||||||
chr8:21954200
|
T | A | 2 | a0001c0005t0002g0148a0001c0005t0002g0153 | 2 | NA18975.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.19-12657T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954200 | ||||||
chr8:21954206
|
T | G | 2 | a0001c0002t0001g0229a0001c0002t0001g0239 | 2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.19-12651T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954206 | ||||||
chr8:21954264
|
A | G | 2 | a0001c0002t0001g0229a0001c0002t0001g0239 | 2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.19-12593A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954264 | ||||||
chr8:21954482
|
A | C | 93 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(90): Show | 101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.19-12375A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954482 | ||||||
chr8:21954484
|
A | G | 1 | a0001c0002t0001g0268 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19-12373A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954484 | ||||||
chr8:21954489
|
C | T | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-12368C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954489 | ||||||
chr8:21954853
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-12004C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954853 | ||||||
chr8:21954872
|
A | G | 1 | a0001c0001t0002g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19-11985A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21954872 | ||||||
chr8:21955203
|
T | C | 1 | a0001c0001t0002g0243 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.19-11654T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955203 | ||||||
chr8:21955219
|
A | AG | 113 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(110): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.19-11638_19-11637i others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955219 | ||||||
chr8:21955507
|
A | G | 91 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(88): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-11350A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955507 | ||||||
chr8:21955629
|
C | T | 90 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(87): Show | 98 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.19-11228C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955629 | ||||||
chr8:21955724
|
C | CT | 14 | a0001c0001t0002g0011a0001c0001t0002g0145a0001c0001t0002g0146others(11): Show | 15 | HG00438.hp2 HG00558.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-11110dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | |||||
chr8:21955724
|
C | CTT | 19 | a0001c0002t0001g0051a0001c0002t0001g0126a0001c0002t0001g0273others(16): Show | 19 | HG01433.hp1 HG02056.hp2 HG02738.hp2 others(16): Show |
intron_variant | MODIFIER | c.19-11111_19-11110d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | |||||
chr8:21955724
|
C | CTTT | 16 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(13): Show | 18 | HG02451.hp2 HG02572.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-11112_19-11110d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | |||||
chr8:21955724
|
C | CTTTT | 33 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(30): Show | 37 | HG00733.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.19-11113_19-11110d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | |||||
chr8:21955724
|
C | CTTTTT | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0306others(19): Show | 24 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.19-11114_19-11110d others(7): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | |||||
chr8:21955724
|
CTTTTTT | C | 88 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(85): Show | 91 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.19-11115_19-11110d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | |||||
chr8:21955724
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-11120_19-11110d others(13): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21955724 | |||||
chr8:21955925
|
C | T | 1 | a0001c0002t0004g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.19-10932C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21955925 | ||||||
chr8:21956224
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.19-10633C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956224 | ||||||
chr8:21956300
|
G | T | 1 | a0001c0002t0001g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.19-10557G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956300 | ||||||
chr8:21956396
|
T | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-10461T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956396 | ||||||
chr8:21956451
|
A | G | 92 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(89): Show | 95 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-10406A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956451 | ||||||
chr8:21956477
|
T | C | 1 | a0001c0001t0002g0186 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.19-10380T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956477 | ||||||
chr8:21956493
|
A | G | 185 | a0001c0001t0002g0010a0001c0002t0001g0003a0001c0002t0001g0012others(182): Show | 197 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.19-10364A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956493 | ||||||
chr8:21956546
|
G | C | 2 | a0001c0002t0001g0259a0001c0002t0001g0267 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.19-10311G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956546 | ||||||
chr8:21956645
|
CT | C | 182 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(179): Show | 193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.19-10208delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21956645 | |||||
chr8:21956652
|
T | A | 2 | a0001c0002t0001g0252a0003c0012t0001g0251 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.19-10205T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956652 | ||||||
chr8:21956952
|
A | G | 1 | a0001c0002t0001g0308 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.19-9905A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21956952 | ||||||
chr8:21957063
|
T | C | 1 | a0001c0003t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.19-9794T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957063 | ||||||
chr8:21957104
|
C | G | 6 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(3): Show | 7 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-9753C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957104 | ||||||
chr8:21957162
|
G | T | 1 | a0001c0002t0001g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.19-9695G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957162 | ||||||
chr8:21957210
|
C | G | 2 | a0001c0002t0001g0259a0001c0002t0001g0267 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.19-9647C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957210 | ||||||
chr8:21957214
|
T | G | 10 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(7): Show | 11 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-9643T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957214 | ||||||
chr8:21957221
|
A | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-9636A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957221 | ||||||
chr8:21957227
|
C | T | 1 | a0001c0002t0001g0312 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.19-9630C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957227 | ||||||
chr8:21957228
|
C | T | 90 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(87): Show | 93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-9629C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957228 | ||||||
chr8:21957233
|
G | A | 3 | a0001c0002t0001g0262a0001c0002t0001g0263a0001c0002t0001g0268 | 3 | HG02055.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.19-9624G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957233 | ||||||
chr8:21957259
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.19-9598G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957259 | ||||||
chr8:21957498
|
C | T | 46 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0158others(43): Show | 51 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.19-9359C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957498 | ||||||
chr8:21957499
|
C | T | 1 | a0001c0003t0001g0112 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.19-9358C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957499 | ||||||
chr8:21957527
|
C | A | 1 | a0001c0001t0002g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.19-9330C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957527 | ||||||
chr8:21957662
|
T | A | 1 | a0001c0001t0002g0140 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.19-9195T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957662 | ||||||
chr8:21957693
|
C | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-9164C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957693 | ||||||
chr8:21957803
|
G | T | 21 | a0001c0002t0001g0051a0001c0002t0001g0273a0001c0002t0001g0274others(18): Show | 23 | HG01433.hp1 HG02647.hp2 HG02738.hp2 others(20): Show |
intron_variant | MODIFIER | c.19-9054G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957803 | ||||||
chr8:21957815
|
C | T | 2 | a0001c0002t0001g0229a0001c0002t0001g0239 | 2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.19-9042C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957815 | ||||||
chr8:21957867
|
G | A | 87 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(84): Show | 95 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-8990G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957867 | ||||||
chr8:21957879
|
G | GT | 8 | a0001c0001t0002g0219a0001c0002t0001g0028a0001c0002t0001g0246others(5): Show | 8 | HG02056.hp1 HG02300.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-8968dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21957879 | |||||
chr8:21957914
|
T | G | 113 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(110): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.19-8943T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21957914 | ||||||
chr8:21958022
|
C | T | 1 | a0003c0012t0001g0251 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19-8835C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958022 | ||||||
chr8:21958054
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-8803G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958054 | ||||||
chr8:21958174
|
T | A | 2 | a0001c0003t0001g0063a0001c0003t0001g0067 | 2 | HG00741.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.19-8683T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958174 | ||||||
chr8:21958277
|
C | G | 2 | a0001c0002t0001g0158a0001c0002t0001g0161 | 2 | HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19-8580C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958277 | ||||||
chr8:21958289
|
A | G | 4 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-8568A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958289 | ||||||
chr8:21958359
|
C | A | 2 | a0001c0006t0005g0264a0001c0006t0005g0269 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-8498C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958359 | ||||||
chr8:21958430
|
G | A | 1 | a0001c0002t0001g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.19-8427G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958430 | ||||||
chr8:21958539
|
A | C | 1 | a0001c0002t0001g0284 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.19-8318A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958539 | ||||||
chr8:21958540
|
G | C | 1 | a0001c0002t0001g0284 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.19-8317G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958540 | ||||||
chr8:21958574
|
C | T | 1 | a0001c0002t0008g0271 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19-8283C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958574 | ||||||
chr8:21958602
|
A | G | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-8255A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958602 | ||||||
chr8:21958610
|
G | GA | 23 | a0001c0001t0002g0018a0001c0001t0002g0167a0001c0001t0002g0168others(20): Show | 23 | HG00621.hp2 HG00735.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.19-8235dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21958610 | |||||
chr8:21958643
|
T | G | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-8214T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958643 | ||||||
chr8:21958708
|
CA | C | 324 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(321): Show | 341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.19-8147delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21958708 | |||||
chr8:21958776
|
A | G | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-8081A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958776 | ||||||
chr8:21958812
|
C | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0178 | 2 | NA18983.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.19-8045C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958812 | ||||||
chr8:21958910
|
G | A | 1 | a0001c0002t0001g0280 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.19-7947G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958910 | ||||||
chr8:21958961
|
CA | C | 9 | a0001c0001t0002g0123a0001c0002t0001g0012a0001c0002t0001g0013others(6): Show | 11 | HG01175.hp1 HG01934.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-7879delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21958961 | |||||
chr8:21958961
|
CAA | C | 170 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(167): Show | 179 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.19-7880_19-7879del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21958961 | |||||
chr8:21958973
|
A | G | 1 | a0001c0003t0001g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-7884A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21958973 | ||||||
chr8:21959153
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.19-7704C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959153 | ||||||
chr8:21959498
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-7359C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959498 | ||||||
chr8:21959619
|
T | A | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.19-7238T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959619 | ||||||
chr8:21959734
|
C | T | 182 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(179): Show | 193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.19-7123C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959734 | ||||||
chr8:21959856
|
A | C | 1 | a0001c0001t0002g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-7001A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959856 | ||||||
chr8:21959862
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.19-6995A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959862 | ||||||
chr8:21959869
|
C | T | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19-6988C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959869 | ||||||
chr8:21959895
|
G | A | 4 | a0001c0002t0001g0274a0001c0002t0001g0284a0001c0002t0001g0286others(1): Show | 4 | NA18946.hp2 NA18955.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-6962G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21959895 | ||||||
chr8:21960057
|
G | A | 324 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(321): Show | 341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.19-6800G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960057 | ||||||
chr8:21960104
|
G | A | 315 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(312): Show | 332 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.19-6753G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960104 | ||||||
chr8:21960265
|
C | A | 1 | a0001c0003t0001g0074 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.19-6592C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960265 | ||||||
chr8:21960295
|
G | A | 17 | a0001c0002t0001g0051a0001c0002t0001g0273a0001c0002t0001g0274others(14): Show | 19 | HG01433.hp1 HG02738.hp2 HG03704.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-6562G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960295 | ||||||
chr8:21960296
|
T | G | 1 | a0001c0001t0002g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.19-6561T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960296 | ||||||
chr8:21960479
|
C | G | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-6378C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960479 | ||||||
chr8:21960549
|
A | G | 92 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(89): Show | 95 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-6308A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960549 | ||||||
chr8:21960660
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.19-6197C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960660 | ||||||
chr8:21960699
|
G | A | 2 | a0001c0001t0002g0164a0001c0005t0002g0225 | 2 | HG02155.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.19-6158G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960699 | ||||||
chr8:21960834
|
A | C | 1 | a0001c0001t0002g0197 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.19-6023A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21960834 | ||||||
chr8:21961204
|
G | GT | 7 | a0001c0001t0002g0147a0001c0001t0002g0215a0001c0002t0001g0316others(4): Show | 7 | HG01358.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5638dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21961204 | |||||
chr8:21961390
|
A | G | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-5467A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961390 | ||||||
chr8:21961405
|
G | A | 1 | a0001c0002t0005g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-5452G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961405 | ||||||
chr8:21961412
|
C | T | 1 | a0001c0002t0005g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-5445C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961412 | ||||||
chr8:21961464
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19-5393C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961464 | ||||||
chr8:21961687
|
G | C | 1 | a0001c0001t0002g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.19-5170G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961687 | ||||||
chr8:21961774
|
G | A | 26 | a0001c0002t0001g0282a0001c0002t0001g0285a0001c0002t0001g0299others(23): Show | 28 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-5083G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961774 | ||||||
chr8:21961854
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0220a0004c0011t0002g0165 | 3 | HG03041.hp1 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19-5003G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961854 | ||||||
chr8:21961855
|
GT | G | 56 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(53): Show | 62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.19-4999delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21961855 | |||||
chr8:21961864
|
C | T | 2 | a0001c0003t0001g0079a0001c0003t0001g0080 | 2 | HG02165.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.19-4993C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961864 | ||||||
chr8:21961965
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.19-4892A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21961965 | ||||||
chr8:21962084
|
C | T | 1 | a0001c0003t0001g0111 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.19-4773C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962084 | ||||||
chr8:21962266
|
C | T | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19-4591C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962266 | ||||||
chr8:21962470
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-4387T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962470 | ||||||
chr8:21962514
|
G | A | 17 | a0001c0002t0001g0051a0001c0002t0001g0273a0001c0002t0001g0274others(14): Show | 19 | HG01433.hp1 HG02738.hp2 HG03704.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-4343G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962514 | ||||||
chr8:21962517
|
G | C | 1 | a0001c0001t0002g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-4340G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962517 | ||||||
chr8:21962531
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.19-4326A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962531 | ||||||
chr8:21962566
|
C | A | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-4291C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962566 | ||||||
chr8:21962602
|
CA | C | 5 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-4254delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962602 | ||||||
chr8:21962724
|
T | G | 1 | a0001c0003t0002g0295 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-4133T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962724 | ||||||
chr8:21962968
|
A | T | 89 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(86): Show | 92 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.19-3889A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21962968 | ||||||
chr8:21963257
|
G | T | 1 | a0001c0001t0002g0137 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.19-3600G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963257 | ||||||
chr8:21963302
|
C | A | 91 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(88): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-3555C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963302 | ||||||
chr8:21963637
|
G | T | 1 | a0001c0003t0001g0101 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.19-3220G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963637 | ||||||
chr8:21963643
|
C | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-3214C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963643 | ||||||
chr8:21963694
|
CA | C | 110 | a0001c0001t0002g0010a0001c0002t0001g0046a0001c0002t0001g0051others(107): Show | 116 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-3147delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21963694 | |||||
chr8:21963694
|
CAA | C | 69 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(66): Show | 75 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.19-3148_19-3147del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21963694 | |||||
chr8:21963760
|
C | T | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-3097C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21963760 | ||||||
chr8:21964147
|
A | G | 1 | a0001c0002t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19-2710A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964147 | ||||||
chr8:21964150
|
G | A | 1 | a0001c0004t0001g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.19-2707G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964150 | ||||||
chr8:21964220
|
G | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-2637G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964220 | ||||||
chr8:21964267
|
G | T | 87 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(84): Show | 95 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-2590G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964267 | ||||||
chr8:21964275
|
G | T | 6 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(3): Show | 7 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-2582G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964275 | ||||||
chr8:21964338
|
C | T | 1 | a0001c0002t0005g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-2519C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964338 | ||||||
chr8:21964514
|
C | T | 3 | a0001c0002t0006g0318a0001c0002t0006g0319a0001c0002t0006g0320 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.19-2343C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964514 | ||||||
chr8:21964515
|
G | A | 1 | a0001c0003t0001g0081 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.19-2342G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964515 | ||||||
chr8:21964539
|
A | T | 1 | a0001c0001t0002g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.19-2318A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964539 | ||||||
chr8:21964562
|
C | T | 2 | a0001c0002t0001g0299a0001c0002t0001g0312 | 2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.19-2295C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964562 | ||||||
chr8:21964613
|
CA | C | 75 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(72): Show | 81 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-2232delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21964613 | |||||
chr8:21964613
|
CAA | C | 6 | a0001c0002t0001g0051a0001c0002t0001g0273a0001c0002t0004g0001others(3): Show | 8 | HG01433.hp1 HG04115.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-2233_19-2232del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21964613 | |||||
chr8:21964667
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-2190G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964667 | ||||||
chr8:21964853
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0218 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.19-2004G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21964853 | ||||||
chr8:21965119
|
C | G | 8 | a0001c0002t0001g0293a0001c0002t0005g0258a0001c0002t0005g0261others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-1738C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965119 | ||||||
chr8:21965208
|
C | T | 3 | a0001c0002t0001g0229a0001c0002t0001g0230a0001c0002t0001g0239 | 3 | NA18940.hp2 NA18950.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.19-1649C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965208 | ||||||
chr8:21965276
|
A | G | 1 | a0001c0003t0001g0031 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19-1581A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965276 | ||||||
chr8:21965391
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.19-1466A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965391 | ||||||
chr8:21965471
|
G | T | 1 | a0001c0002t0009g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-1386G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965471 | ||||||
chr8:21965514
|
G | A | 91 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(88): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.19-1343G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965514 | ||||||
chr8:21965533
|
A | G | 1 | a0001c0003t0003g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.19-1324A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965533 | ||||||
chr8:21965556
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0156 | 2 | NA18978.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.19-1301C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965556 | ||||||
chr8:21965603
|
A | G | 1 | a0001c0003t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.19-1254A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965603 | ||||||
chr8:21965638
|
C | T | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-1219C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965638 | ||||||
chr8:21965662
|
G | C | 88 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(85): Show | 96 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.19-1195G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965662 | ||||||
chr8:21965663
|
T | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-1194T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965663 | ||||||
chr8:21965673
|
A | G | 113 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(110): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.19-1184A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965673 | ||||||
chr8:21965695
|
T | G | 113 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(110): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.19-1162T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965695 | ||||||
chr8:21965750
|
C | T | 1 | a0001c0003t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.19-1107C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965750 | ||||||
chr8:21965758
|
A | G | 1 | a0001c0002t0001g0245 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.19-1099A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965758 | ||||||
chr8:21965949
|
A | G | 3 | a0001c0002t0001g0293a0001c0006t0005g0264a0001c0006t0005g0269 | 3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.19-908A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965949 | ||||||
chr8:21965976
|
C | T | 88 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(85): Show | 96 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.19-881C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21965976 | ||||||
chr8:21965980
|
C | CCACTT | 205 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(202): Show | 217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.19-875_19-874insCT others(3): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21965980 | |||||
chr8:21966136
|
A | G | 1 | a0001c0002t0001g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.19-721A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966136 | ||||||
chr8:21966374
|
C | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-483C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966374 | ||||||
chr8:21966466
|
G | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.19-391G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966466 | ||||||
chr8:21966552
|
C | T | 1 | a0001c0002t0005g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-305C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966552 | ||||||
chr8:21966590
|
G | A | 8 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0005g0258others(5): Show | 10 | HG02109.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-267G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966590 | ||||||
chr8:21966626
|
A | G | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-231A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966626 | ||||||
chr8:21966636
|
AG | A | 10 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(7): Show | 11 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-220delG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966636 | ||||||
chr8:21966637
|
GT | G | 171 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0029others(168): Show | 181 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.19-218delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr8 | 21966637 | |||||
chr8:21966638
|
T | A | 10 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(7): Show | 11 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-219T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 1/27 | chr8 | 21966638 | ||||||
chr8:21967036
|
A | G | 187 | a0001c0001t0002g0010a0001c0002t0001g0003a0001c0002t0001g0012others(184): Show | 199 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.165+33A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967036 | ||||||
chr8:21967087
|
G | A | 1 | a0001c0002t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.165+84G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967087 | ||||||
chr8:21967246
|
C | T | 2 | a0001c0002t0001g0299a0001c0002t0001g0312 | 2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.165+243C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967246 | ||||||
chr8:21967368
|
T | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.165+365T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967368 | ||||||
chr8:21967629
|
G | A | 1 | a0001c0002t0001g0257 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165+626G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967629 | ||||||
chr8:21967768
|
A | C | 1 | a0001c0009t0002g0075 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.165+765A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967768 | ||||||
chr8:21967852
|
A | G | 1 | a0001c0003t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+849A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967852 | ||||||
chr8:21967892
|
G | C | 3 | a0001c0001t0002g0157a0001c0001t0002g0198a0001c0001t0002g0201 | 3 | HG02040.hp2 HG02165.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.165+889G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967892 | ||||||
chr8:21967968
|
G | C | 3 | a0001c0004t0001g0014a0001c0004t0001g0296a0001c0004t0001g0311 | 4 | HG01070.hp1 HG01071.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+965G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21967968 | ||||||
chr8:21968064
|
C | T | 4 | a0001c0002t0001g0051a0001c0002t0004g0001a0001c0002t0004g0049others(1): Show | 6 | NA18947.hp2 NA18957.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1061C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968064 | ||||||
chr8:21968246
|
A | T | 1 | a0001c0001t0002g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.166-1237A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968246 | ||||||
chr8:21968380
|
G | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-1103G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968380 | ||||||
chr8:21968424
|
A | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.166-1059A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968424 | ||||||
chr8:21968462
|
C | G | 1 | a0001c0003t0001g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.166-1021C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968462 | ||||||
chr8:21968507
|
G | A | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.166-976G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968507 | ||||||
chr8:21968592
|
A | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.166-891A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968592 | ||||||
chr8:21968786
|
T | C | 7 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(4): Show | 7 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-697T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968786 | ||||||
chr8:21968838
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.166-645G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968838 | ||||||
chr8:21968910
|
C | T | 181 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(178): Show | 192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.166-573C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21968910 | ||||||
chr8:21969181
|
A | G | 13 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(10): Show | 14 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-302A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969181 | ||||||
chr8:21969210
|
T | G | 1 | a0001c0002t0001g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.166-273T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969210 | ||||||
chr8:21969309
|
TTATGC | T | 87 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(84): Show | 95 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.166-169_166-165del others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr8 | 21969309 | |||||
chr8:21969316
|
A | G | 3 | a0001c0002t0001g0237a0001c0002t0001g0259a0001c0002t0001g0267 | 3 | HG01358.hp2 HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.166-167A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969316 | ||||||
chr8:21969316
|
A | T | 1 | a0001c0001t0002g0130 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.166-167A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969316 | ||||||
chr8:21969428
|
T | C | 3 | a0001c0004t0001g0015a0001c0004t0001g0297a0001c0004t0001g0313 | 4 | HG00323.hp1 HG01069.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-55T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 2/27 | chr8 | 21969428 | ||||||
chr8:21969598
|
C | T | 11 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(8): Show | 12 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+22C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969598 | ||||||
chr8:21969651
|
C | T | 93 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(90): Show | 96 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.259+75C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969651 | ||||||
chr8:21969722
|
T | G | 1 | a0001c0002t0006g0318 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.259+146T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969722 | ||||||
chr8:21969734
|
A | G | 2 | a0001c0006t0005g0264a0001c0006t0005g0269 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.259+158A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969734 | ||||||
chr8:21969880
|
G | A | 86 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(83): Show | 94 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.260-264G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969880 | ||||||
chr8:21969947
|
A | G | 3 | a0001c0002t0001g0282a0001c0002t0001g0285a0001c0002t0002g0283 | 3 | HG03688.hp1 HG03927.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.260-197A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21969947 | ||||||
chr8:21970044
|
A | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.260-100A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 3/27 | chr8 | 21970044 | ||||||
chr8:21970322
|
A | G | 110 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(107): Show | 114 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.426+12A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970322 | ||||||
chr8:21970364
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.426+54A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970364 | ||||||
chr8:21970369
|
A | AAC | 13 | a0001c0001t0002g0175a0001c0001t0002g0182a0001c0001t0002g0196others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.426+81_426+82dupCA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970369 | |||||
chr8:21970369
|
A | AACAC | 104 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(101): Show | 106 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.426+79_426+82dupCA others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970369 | |||||
chr8:21970369
|
A | AACACAC | 8 | a0001c0003t0001g0002a0001c0003t0001g0054a0001c0003t0001g0071others(5): Show | 10 | HG02027.hp2 HG02083.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.426+77_426+82dupCA others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970369 | |||||
chr8:21970661
|
C | T | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.426+351C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970661 | ||||||
chr8:21970715
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.426+405A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970715 | ||||||
chr8:21970751
|
G | A | 1 | a0001c0002t0001g0155 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.426+441G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970751 | ||||||
chr8:21970784
|
C | T | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.426+474C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970784 | ||||||
chr8:21970795
|
A | G | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.426+485A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970795 | ||||||
chr8:21970805
|
G | GA | 7 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+503dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr8 | 21970805 | |||||
chr8:21970932
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.426+622C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21970932 | ||||||
chr8:21971007
|
G | C | 6 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(3): Show | 7 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.426+697G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971007 | ||||||
chr8:21971036
|
A | T | 1 | a0001c0002t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.426+726A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971036 | ||||||
chr8:21971111
|
T | C | 1 | a0001c0002t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.427-765T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971111 | ||||||
chr8:21971133
|
G | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.427-743G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971133 | ||||||
chr8:21971270
|
G | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0215 | 2 | NA19000.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.427-606G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971270 | ||||||
chr8:21971347
|
C | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.427-529C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971347 | ||||||
chr8:21971477
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.427-399G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971477 | ||||||
chr8:21971574
|
C | G | 2 | a0001c0002t0001g0252a0003c0012t0001g0251 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.427-302C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971574 | ||||||
chr8:21971712
|
T | C | 1 | a0001c0002t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.427-164T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971712 | ||||||
chr8:21971822
|
G | A | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.427-54G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 4/27 | chr8 | 21971822 | ||||||
chr8:21972176
|
C | CT | 21 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(18): Show | 23 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.492+247dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21972176 | |||||
chr8:21972304
|
C | G | 1 | a0001c0002t0001g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.492+363C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972304 | ||||||
chr8:21972360
|
TC | T | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.492+422delC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21972360 | |||||
chr8:21972437
|
G | A | 186 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(183): Show | 197 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.492+496G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972437 | ||||||
chr8:21972525
|
A | C | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.492+584A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972525 | ||||||
chr8:21972579
|
T | C | 1 | a0001c0002t0005g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.492+638T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972579 | ||||||
chr8:21972647
|
T | C | 188 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(185): Show | 199 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.492+706T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972647 | ||||||
chr8:21972686
|
A | G | 3 | a0001c0002t0001g0160a0001c0002t0001g0217a0001c0002t0007g0009 | 4 | HG02280.hp2 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+745A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972686 | ||||||
chr8:21972784
|
A | G | 96 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(93): Show | 104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.492+843A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972784 | ||||||
chr8:21972867
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.492+926G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21972867 | ||||||
chr8:21973019
|
A | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01934.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.492+1078A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973019 | ||||||
chr8:21973027
|
C | A | 3 | a0001c0003t0001g0032a0001c0003t0001g0060a0001c0003t0001g0061 | 3 | HG01167.hp2 HG03654.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.492+1086C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973027 | ||||||
chr8:21973033
|
A | AG | 5 | a0001c0001t0002g0010a0001c0001t0002g0167a0001c0001t0002g0219others(2): Show | 6 | HG00738.hp1 HG01099.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+1094dupG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21973033 | |||||
chr8:21973291
|
A | G | 1 | a0001c0003t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.492+1350A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973291 | ||||||
chr8:21973621
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.493-1049G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973621 | ||||||
chr8:21973634
|
T | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.493-1036T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973634 | ||||||
chr8:21973738
|
A | C | 2 | a0001c0003t0001g0088a0001c0003t0001g0109 | 2 | HG00735.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.493-932A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973738 | ||||||
chr8:21973865
|
G | A | 45 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0158others(42): Show | 50 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.493-805G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973865 | ||||||
chr8:21973874
|
A | G | 88 | a0001c0003t0001g0002a0001c0003t0001g0004a0001c0003t0001g0031others(85): Show | 91 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.493-796A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973874 | ||||||
chr8:21973972
|
C | A | 1 | a0001c0001t0002g0141 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.493-698C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973972 | ||||||
chr8:21973993
|
CTT | C | 3 | a0001c0002t0005g0258a0001c0002t0005g0265a0001c0002t0005g0294 | 3 | HG03195.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.493-676_493-675del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973993 | ||||||
chr8:21973999
|
C | A | 45 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0158others(42): Show | 50 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.493-671C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21973999 | ||||||
chr8:21974087
|
G | GACAGGAT others(3): Show |
206 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(203): Show | 218 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.493-581_493-580ins others(10): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21974087 | |||||
chr8:21974107
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.493-563A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21974107 | ||||||
chr8:21974208
|
T | G | 1 | a0001c0003t0001g0054 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.493-462T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21974208 | ||||||
chr8:21974231
|
T | TG | 103 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(100): Show | 107 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.493-433dupG | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr8 | 21974231 | |||||
chr8:21974554
|
G | T | 1 | a0001c0003t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.493-116G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 5/27 | chr8 | 21974554 | ||||||
chr8:21974983
|
A | C | 212 | a0001c0001t0002g0164a0001c0001t0002g0248a0001c0002t0001g0003others(209): Show | 224 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.597+209A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21974983 | ||||||
chr8:21975305
|
T | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.597+531T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975305 | ||||||
chr8:21975430
|
C | G | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.597+656C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975430 | ||||||
chr8:21975467
|
A | G | 1 | a0001c0002t0005g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597+693A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975467 | ||||||
chr8:21975575
|
C | T | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.598-781C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975575 | ||||||
chr8:21975729
|
C | G | 13 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(10): Show | 14 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.598-627C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975729 | ||||||
chr8:21975863
|
G | C | 93 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(90): Show | 101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.598-493G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21975863 | ||||||
chr8:21976336
|
T | C | 1 | a0001c0006t0005g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.598-20T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 6/27 | chr8 | 21976336 | ||||||
chr8:21976532
|
T | C | 1 | a0001c0003t0001g0111 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.763+11T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976532 | ||||||
chr8:21976855
|
A | C | 188 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(185): Show | 199 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.763+334A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976855 | ||||||
chr8:21976893
|
A | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.763+372A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976893 | ||||||
chr8:21976895
|
G | C | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.763+374G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976895 | ||||||
chr8:21976932
|
T | G | 1 | a0001c0003t0001g0068 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.763+411T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976932 | ||||||
chr8:21976945
|
C | G | 96 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(93): Show | 104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.763+424C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21976945 | ||||||
chr8:21977004
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.763+483C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977004 | ||||||
chr8:21977056
|
A | G | 88 | a0001c0003t0001g0002a0001c0003t0001g0004a0001c0003t0001g0031others(85): Show | 91 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.763+535A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977056 | ||||||
chr8:21977070
|
T | C | 191 | a0001c0001t0002g0010a0001c0002t0001g0003a0001c0002t0001g0012others(188): Show | 203 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.763+549T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977070 | ||||||
chr8:21977303
|
G | A | 31 | a0001c0002t0001g0024a0001c0002t0001g0299a0001c0002t0001g0300others(28): Show | 33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.764-467G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977303 | ||||||
chr8:21977490
|
A | G | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.764-280A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977490 | ||||||
chr8:21977567
|
A | C | 1 | a0001c0002t0005g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.764-203A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977567 | ||||||
chr8:21977706
|
G | A | 1 | a0001c0002t0005g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.764-64G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 7/27 | chr8 | 21977706 | ||||||
chr8:21977859
|
C | T | 2 | a0001c0002t0001g0259a0001c0002t0001g0267 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.837+16C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21977859 | ||||||
chr8:21977930
|
A | G | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.837+87A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21977930 | ||||||
chr8:21977954
|
A | G | 88 | a0001c0003t0001g0002a0001c0003t0001g0004a0001c0003t0001g0031others(85): Show | 91 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.837+111A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21977954 | ||||||
chr8:21978041
|
C | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.837+198C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978041 | ||||||
chr8:21978043
|
G | T | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.837+200G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978043 | ||||||
chr8:21978074
|
C | CT | 96 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(93): Show | 104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.837+232dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21978074 | |||||
chr8:21978117
|
A | G | 88 | a0001c0003t0001g0002a0001c0003t0001g0004a0001c0003t0001g0031others(85): Show | 91 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.837+274A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978117 | ||||||
chr8:21978307
|
T | C | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.837+464T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978307 | ||||||
chr8:21978396
|
G | A | 95 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(92): Show | 103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.837+553G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978396 | ||||||
chr8:21978509
|
A | G | 54 | a0001c0003t0001g0071a0001c0003t0001g0072a0001c0003t0001g0074others(51): Show | 54 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.837+666A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978509 | ||||||
chr8:21978838
|
G | A | 2 | a0001c0002t0001g0253a0001c0002t0001g0254 | 2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.837+995G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978838 | ||||||
chr8:21978873
|
C | G | 90 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0003t0001g0002others(87): Show | 93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.837+1030C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978873 | ||||||
chr8:21978875
|
A | T | 1 | a0001c0002t0004g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.837+1032A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21978875 | ||||||
chr8:21979203
|
G | A | 2 | a0001c0002t0001g0259a0001c0002t0001g0267 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.838-881G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979203 | ||||||
chr8:21979217
|
A | G | 188 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(185): Show | 199 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.838-867A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979217 | ||||||
chr8:21979382
|
ATTTCTTT others(4): Show |
A | 1 | a0001c0001t0002g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.838-687_838-677del others(11): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21979382 | |||||
chr8:21979397
|
C | CT | 9 | a0001c0002t0001g0280a0001c0002t0001g0281a0001c0002t0001g0282others(6): Show | 9 | HG02738.hp2 HG03688.hp1 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.838-676dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21979397 | |||||
chr8:21979397
|
C | T | 1 | a0001c0002t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.838-687C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979397 | ||||||
chr8:21979410
|
G | GT | 10 | a0001c0001t0002g0135a0001c0001t0002g0146a0001c0001t0002g0206others(7): Show | 10 | HG00738.hp2 HG02056.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.838-665dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr8 | 21979410 | |||||
chr8:21979712
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0002g0212 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.838-372G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 8/27 | chr8 | 21979712 | ||||||
chr8:21980290
|
G | A | 2 | a0001c0002t0001g0253a0001c0002t0001g0254 | 2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.957+87G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980290 | ||||||
chr8:21980367
|
A | C | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+164A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980367 | ||||||
chr8:21980410
|
A | G | 1 | a0001c0002t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.957+207A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980410 | ||||||
chr8:21980483
|
C | G | 93 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(90): Show | 101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.957+280C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980483 | ||||||
chr8:21980638
|
G | A | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.957+435G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980638 | ||||||
chr8:21980769
|
C | T | 2 | a0001c0002t0001g0046a0001c0002t0001g0065 | 2 | HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.957+566C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980769 | ||||||
chr8:21980774
|
C | CA | 8 | a0001c0002t0001g0246a0001c0002t0001g0279a0001c0002t0002g0250others(5): Show | 8 | HG02056.hp2 HG02071.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.957+587dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr8 | 21980774 | |||||
chr8:21980778
|
A | G | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.957+575A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980778 | ||||||
chr8:21980831
|
A | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.957+628A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980831 | ||||||
chr8:21980870
|
G | A | 3 | a0001c0002t0001g0160a0001c0002t0001g0217a0001c0002t0007g0009 | 4 | HG02280.hp2 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.957+667G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21980870 | ||||||
chr8:21980999
|
C | CA | 113 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(110): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.958-731dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr8 | 21980999 | |||||
chr8:21981159
|
T | A | 210 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(207): Show | 222 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.958-572T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981159 | ||||||
chr8:21981220
|
T | C | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.958-511T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981220 | ||||||
chr8:21981274
|
T | C | 1 | a0001c0002t0005g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.958-457T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981274 | ||||||
chr8:21981278
|
T | C | 95 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(92): Show | 103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.958-453T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981278 | ||||||
chr8:21981327
|
C | T | 2 | a0001c0002t0001g0013a0001c0003t0001g0093 | 3 | HG02109.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.958-404C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981327 | ||||||
chr8:21981357
|
T | G | 10 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.958-374T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981357 | ||||||
chr8:21981468
|
C | G | 3 | a0001c0002t0001g0262a0001c0002t0001g0263a0001c0002t0001g0268 | 3 | HG02055.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.958-263C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981468 | ||||||
chr8:21981509
|
T | C | 95 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(92): Show | 103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.958-222T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981509 | ||||||
chr8:21981524
|
A | G | 6 | a0001c0002t0005g0258a0001c0002t0005g0265a0001c0002t0005g0266others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-207A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981524 | ||||||
chr8:21981582
|
T | G | 95 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(92): Show | 103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.958-149T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981582 | ||||||
chr8:21981589
|
G | A | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.958-142G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981589 | ||||||
chr8:21981603
|
C | T | 3 | a0001c0002t0006g0318a0001c0002t0006g0319a0001c0002t0006g0320 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.958-128C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981603 | ||||||
chr8:21981662
|
A | C | 1 | a0001c0002t0004g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.958-69A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 9/27 | chr8 | 21981662 | ||||||
chr8:21982157
|
G | A | 93 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(90): Show | 101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1104+280G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982157 | ||||||
chr8:21982213
|
T | C | 1 | a0001c0002t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1104+336T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982213 | ||||||
chr8:21982254
|
A | C | 1 | a0001c0001t0002g0130 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1104+377A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982254 | ||||||
chr8:21982368
|
A | G | 1 | a0001c0003t0001g0035 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1105-272A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982368 | ||||||
chr8:21982400
|
T | C | 4 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0217others(1): Show | 5 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105-240T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982400 | ||||||
chr8:21982410
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1105-230T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982410 | ||||||
chr8:21982486
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01934.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1105-154A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982486 | ||||||
chr8:21982541
|
T | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1105-99T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982541 | ||||||
chr8:21982541
|
T | TA | 110 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(107): Show | 114 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1105-91dupA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr8 | 21982541 | |||||
chr8:21982542
|
A | T | 1 | a0001c0002t0001g0263 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1105-98A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982542 | ||||||
chr8:21982568
|
C | G | 1 | a0001c0002t0001g0309 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1105-72C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 10/27 | chr8 | 21982568 | ||||||
chr8:21982858
|
T | C | 1 | a0001c0003t0001g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1277+46T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21982858 | ||||||
chr8:21982899
|
A | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1277+87A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21982899 | ||||||
chr8:21982908
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1277+96G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21982908 | ||||||
chr8:21983023
|
A | G | 116 | a0001c0002t0001g0006a0001c0002t0001g0029a0001c0002t0001g0030others(113): Show | 120 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1277+211A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983023 | ||||||
chr8:21983212
|
G | A | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1277+400G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983212 | ||||||
chr8:21983327
|
C | T | 1 | a0003c0012t0001g0251 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1277+515C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983327 | ||||||
chr8:21983397
|
A | G | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1277+585A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983397 | ||||||
chr8:21983504
|
A | G | 1 | a0001c0002t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1277+692A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983504 | ||||||
chr8:21983586
|
T | G | 1 | a0001c0009t0002g0075 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1277+774T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983586 | ||||||
chr8:21983587
|
T | C | 1 | a0001c0009t0002g0075 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1277+775T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983587 | ||||||
chr8:21983666
|
T | C | 2 | a0001c0006t0005g0264a0001c0006t0005g0269 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1277+854T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983666 | ||||||
chr8:21983682
|
C | T | 1 | a0001c0003t0001g0079 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1277+870C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983682 | ||||||
chr8:21983844
|
GTGCTGCT others(11): Show |
G | 1 | a0001c0004t0001g0296 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1278-791_1278-774d others(20): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 21983844 | |||||
chr8:21983852
|
GCTC | G | 3 | a0001c0002t0006g0318a0001c0002t0006g0319a0001c0002t0006g0320 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1278-791_1278-789d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 21983852 | |||||
chr8:21983855
|
CCTGCTG | C | 50 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(47): Show | 56 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1278-777_1278-772d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr8 | 21983855 | |||||
chr8:21983861
|
G | C | 3 | a0001c0002t0006g0318a0001c0002t0006g0319a0001c0002t0006g0320 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1278-785G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983861 | ||||||
chr8:21983885
|
T | C | 211 | a0001c0001t0002g0010a0001c0002t0001g0003a0001c0002t0001g0006others(208): Show | 224 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1278-761T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983885 | ||||||
chr8:21983965
|
C | A | 1 | a0001c0002t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1278-681C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21983965 | ||||||
chr8:21984037
|
A | G | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278-609A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984037 | ||||||
chr8:21984065
|
C | T | 2 | a0001c0002t0001g0022a0001c0002t0001g0028 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1278-581C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984065 | ||||||
chr8:21984099
|
A | T | 1 | a0001c0002t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1278-547A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984099 | ||||||
chr8:21984110
|
T | C | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1278-536T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984110 | ||||||
chr8:21984153
|
G | T | 2 | a0001c0002t0004g0290a0001c0002t0004g0291 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1278-493G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984153 | ||||||
chr8:21984186
|
G | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1278-460G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984186 | ||||||
chr8:21984203
|
A | G | 1 | a0001c0001t0002g0204 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1278-443A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984203 | ||||||
chr8:21984352
|
C | G | 188 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(185): Show | 199 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1278-294C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984352 | ||||||
chr8:21984512
|
T | G | 322 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(319): Show | 339 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.1278-134T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984512 | ||||||
chr8:21984513
|
T | A | 323 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(320): Show | 340 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.1278-133T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984513 | ||||||
chr8:21984552
|
T | C | 113 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0002t0001g0064others(110): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1278-94T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984552 | ||||||
chr8:21984628
|
T | C | 1 | a0001c0003t0001g0043 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1278-18T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 11/27 | chr8 | 21984628 | ||||||
chr8:21984882
|
T | C | 3 | a0001c0002t0001g0275a0001c0002t0001g0277a0001c0002t0001g0288 | 3 | NA18612.hp1 NA19000.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1471+43T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21984882 | ||||||
chr8:21984974
|
A | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0216a0001c0001t0010g0144 | 3 | NA18984.hp2 NA18997.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1471+135A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21984974 | ||||||
chr8:21985074
|
G | GC | 208 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(205): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1471+237dupC | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr8 | 21985074 | |||||
chr8:21985079
|
G | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1471+240G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985079 | ||||||
chr8:21985217
|
G | C | 95 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(92): Show | 103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.1472-369G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985217 | ||||||
chr8:21985240
|
G | C | 210 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(207): Show | 222 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1472-346G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985240 | ||||||
chr8:21985564
|
C | G | 3 | a0001c0002t0001g0272a0001c0002t0001g0289a0001c0002t0008g0271 | 3 | HG04115.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1472-22C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 12/27 | chr8 | 21985564 | ||||||
chr8:21985781
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1577+90T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21985781 | ||||||
chr8:21986134
|
A | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1577+443A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986134 | ||||||
chr8:21986135
|
C | CT | 10 | a0001c0001t0002g0018a0001c0002t0001g0046a0001c0002t0001g0065others(7): Show | 10 | HG01169.hp2 HG02300.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1577+463dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr8 | 21986135 | |||||
chr8:21986135
|
CT | C | 23 | a0001c0001t0002g0131a0001c0002t0001g0051a0001c0002t0001g0158others(20): Show | 26 | HG01433.hp1 HG02055.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.1577+463delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr8 | 21986135 | |||||
chr8:21986135
|
CTT | C | 14 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276others(11): Show | 14 | HG02738.hp2 HG03688.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.1577+462_1577+463d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr8 | 21986135 | |||||
chr8:21986178
|
C | T | 1 | a0001c0002t0001g0275 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1577+487C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986178 | ||||||
chr8:21986224
|
G | A | 1 | a0001c0003t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1577+533G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986224 | ||||||
chr8:21986463
|
A | T | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1578-678A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986463 | ||||||
chr8:21986484
|
T | G | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1578-657T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986484 | ||||||
chr8:21986585
|
T | C | 23 | a0001c0003t0001g0002a0001c0003t0001g0004a0001c0003t0001g0031others(20): Show | 26 | HG00323.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1578-556T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986585 | ||||||
chr8:21986663
|
G | A | 1 | a0001c0002t0005g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1578-478G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986663 | ||||||
chr8:21986754
|
A | G | 189 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(186): Show | 200 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1578-387A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986754 | ||||||
chr8:21986971
|
T | C | 1 | a0001c0004t0001g0304 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1578-170T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21986971 | ||||||
chr8:21987022
|
G | C | 1 | a0001c0002t0009g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1578-119G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21987022 | ||||||
chr8:21987032
|
G | C | 1 | a0001c0001t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1578-109G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21987032 | ||||||
chr8:21987066
|
G | A | 4 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-75G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 13/27 | chr8 | 21987066 | ||||||
chr8:21987353
|
G | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1713+77G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 14/27 | chr8 | 21987353 | ||||||
chr8:21987380
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1713+104C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 14/27 | chr8 | 21987380 | ||||||
chr8:21987391
|
A | G | 9 | a0001c0003t0001g0074a0001c0003t0001g0076a0001c0003t0001g0078others(6): Show | 9 | NA18747.hp1 NA18944.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+115A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 14/27 | chr8 | 21987391 | ||||||
chr8:21987917
|
T | C | 207 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(204): Show | 219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1787+60T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21987917 | ||||||
chr8:21988108
|
G | T | 93 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(90): Show | 101 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1787+251G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988108 | ||||||
chr8:21988226
|
G | T | 2 | a0001c0003t0003g0087a0001c0003t0003g0104 | 2 | NA18942.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1787+369G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988226 | ||||||
chr8:21988237
|
G | A | 1 | a0001c0001t0002g0005 | 2 | NA18959.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1787+380G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988237 | ||||||
chr8:21988344
|
G | A | 26 | a0001c0002t0001g0051a0001c0002t0001g0126a0001c0002t0001g0272others(23): Show | 28 | HG01433.hp1 HG02056.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1787+487G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988344 | ||||||
chr8:21988385
|
A | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1787+528A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 15/27 | chr8 | 21988385 | ||||||
chr8:21989275
|
G | A | 1 | a0001c0003t0001g0096 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1868+192G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989275 | ||||||
chr8:21989356
|
A | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1868+273A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989356 | ||||||
chr8:21989477
|
A | T | 1 | a0001c0001t0002g0011 | 2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1868+394A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989477 | ||||||
chr8:21989492
|
C | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0021a0001c0001t0002g0143others(4): Show | 8 | HG01257.hp2 HG01258.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1868+409C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989492 | ||||||
chr8:21989514
|
A | G | 1 | a0001c0003t0001g0096 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1868+431A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989514 | ||||||
chr8:21989724
|
T | C | 208 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(205): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1869-620T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989724 | ||||||
chr8:21989820
|
C | G | 208 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(205): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1869-524C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989820 | ||||||
chr8:21989821
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0172a0001c0001t0002g0174 | 2 | HG04115.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1869-486_1869-477d others(12): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0130a0001c0001t0002g0132 | 2 | NA18982.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1869-488_1869-477d others(14): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
C | CTTTTTTT others(7): Show |
1 | a0001c0003t0001g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1869-490_1869-477d others(16): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1869-491_1869-477d others(17): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0002g0122a0001c0003t0001g0034 | 2 | HG01361.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1869-492_1869-477d others(18): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
C | CTTTTTTT others(10): Show |
1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1869-493_1869-477d others(19): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CT | C | 6 | a0001c0002t0001g0155a0001c0002t0001g0239a0001c0002t0001g0242others(3): Show | 6 | HG01255.hp2 NA18962.hp1 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869-477delT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTT | C | 10 | a0001c0001t0002g0146a0001c0001t0002g0193a0001c0001t0002g0200others(7): Show | 10 | HG00621.hp2 HG01928.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1869-478_1869-477d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTT | C | 24 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0163others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1869-479_1869-477d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTT | C | 29 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0018others(26): Show | 31 | HG00438.hp2 HG00621.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869-480_1869-477d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTT | C | 43 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0020others(40): Show | 43 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1869-481_1869-477d others(7): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTT | C | 36 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0010others(33): Show | 39 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1869-482_1869-477d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT | C | 10 | a0001c0001t0002g0162a0001c0001t0002g0196a0001c0003t0001g0040others(7): Show | 10 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1869-483_1869-477d others(9): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0002g0210a0001c0003t0001g0036a0001c0003t0001g0063 | 3 | HG00741.hp1 HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1869-486_1869-477d others(12): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0002g0005a0001c0003t0001g0032a0001c0003t0001g0055 | 4 | NA18959.hp1 NA18962.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869-487_1869-477d others(13): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0001g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1869-489_1869-477d others(15): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0011g0247a0001c0003t0001g0004a0001c0003t0001g0039others(1): Show | 5 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869-490_1869-477d others(16): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0003t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1869-491_1869-477d others(17): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(11): Show |
C | 4 | a0001c0002t0001g0232a0001c0003t0001g0033a0001c0003t0001g0053others(1): Show | 4 | HG00438.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869-494_1869-477d others(20): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0003t0001g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1869-495_1869-477d others(21): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(13): Show |
C | 2 | a0001c0002t0004g0290a0001c0003t0012g0069 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1869-496_1869-477d others(22): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1869-497_1869-477d others(23): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0002g0205a0001c0001t0002g0221 | 2 | HG02155.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1869-498_1869-477d others(24): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(18): Show |
C | 5 | a0001c0003t0001g0002a0001c0003t0001g0031a0001c0003t0001g0054others(2): Show | 7 | HG02027.hp2 HG02083.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869-501_1869-477d others(27): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(19): Show |
C | 2 | a0001c0002t0001g0279a0001c0002t0001g0285 | 2 | HG02056.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1869-502_1869-477d others(28): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(20): Show |
C | 33 | a0001c0002t0001g0051a0001c0002t0001g0126a0001c0002t0001g0159others(30): Show | 36 | HG01358.hp1 HG01433.hp1 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.1869-503_1869-477d others(29): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(21): Show |
C | 61 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(58): Show | 66 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1869-504_1869-477d others(30): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(22): Show |
C | 1 | a0001c0001t0002g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1869-505_1869-477d others(31): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989821
|
CTTTTTTT others(24): Show |
C | 1 | a0001c0003t0001g0118 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1869-507_1869-477d others(33): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr8 | 21989821 | |||||
chr8:21989887
|
T | C | 29 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0051others(26): Show | 31 | HG01433.hp1 HG02056.hp2 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869-457T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989887 | ||||||
chr8:21989905
|
A | G | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869-439A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989905 | ||||||
chr8:21989913
|
G | A | 95 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(92): Show | 103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.1869-431G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989913 | ||||||
chr8:21989932
|
C | T | 4 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0004g0291others(1): Show | 6 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869-412C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21989932 | ||||||
chr8:21990085
|
G | C | 2 | a0001c0003t0001g0099a0001c0003t0001g0100 | 2 | NA18747.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1869-259G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990085 | ||||||
chr8:21990144
|
C | T | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1869-200C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990144 | ||||||
chr8:21990235
|
T | A | 1 | a0001c0003t0001g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1869-109T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990235 | ||||||
chr8:21990236
|
A | T | 4 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0004g0291others(1): Show | 6 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869-108A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990236 | ||||||
chr8:21990301
|
G | A | 2 | a0001c0002t0001g0252a0003c0012t0001g0251 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1869-43G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 16/27 | chr8 | 21990301 | ||||||
chr8:21990464
|
C | T | 2 | a0001c0002t0001g0259a0001c0002t0001g0267 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1932+57C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990464 | ||||||
chr8:21990538
|
A | G | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1932+131A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990538 | ||||||
chr8:21990558
|
C | T | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1932+151C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990558 | ||||||
chr8:21990583
|
C | G | 1 | a0001c0002t0005g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1932+176C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990583 | ||||||
chr8:21990621
|
C | T | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1933-190C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990621 | ||||||
chr8:21990739
|
C | G | 1 | a0001c0001t0002g0173 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1933-72C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 17/27 | chr8 | 21990739 | ||||||
chr8:21991009
|
C | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+90C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991009 | ||||||
chr8:21991018
|
T | C | 1 | a0001c0003t0001g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2041+99T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991018 | ||||||
chr8:21991108
|
T | G | 1 | a0001c0002t0005g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2041+189T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991108 | ||||||
chr8:21991116
|
T | C | 1 | a0001c0002t0005g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2041+197T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991116 | ||||||
chr8:21991119
|
TCCTGAAG others(8): Show |
T | 1 | a0001c0003t0003g0094 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2041+201_2041+215d others(17): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991119 | ||||||
chr8:21991133
|
T | C | 1 | a0001c0001t0002g0130 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2041+214T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991133 | ||||||
chr8:21991173
|
G | T | 1 | a0001c0001t0002g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2041+254G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991173 | ||||||
chr8:21991224
|
A | G | 1 | a0001c0002t0001g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2041+305A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991224 | ||||||
chr8:21991237
|
C | A | 1 | a0001c0003t0001g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2041+318C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991237 | ||||||
chr8:21991303
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2041+384G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991303 | ||||||
chr8:21991321
|
T | A | 209 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(206): Show | 221 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.2041+402T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991321 | ||||||
chr8:21991347
|
T | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2041+428T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991347 | ||||||
chr8:21991372
|
A | T | 3 | a0001c0002t0001g0293a0001c0006t0005g0264a0001c0006t0005g0269 | 3 | HG02055.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2041+453A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991372 | ||||||
chr8:21991497
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2042-371G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991497 | ||||||
chr8:21991689
|
T | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2042-179T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 18/27 | chr8 | 21991689 | ||||||
chr8:21992006
|
G | C | 2 | a0001c0003t0003g0094a0001c0003t0003g0113 | 2 | NA18965.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2148+32G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992006 | ||||||
chr8:21992055
|
C | T | 75 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2148+81C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992055 | ||||||
chr8:21992205
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2148+231T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992205 | ||||||
chr8:21992386
|
T | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2148+412T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992386 | ||||||
chr8:21992451
|
T | C | 110 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(107): Show | 114 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2148+477T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992451 | ||||||
chr8:21992605
|
A | G | 211 | a0001c0001t0002g0010a0001c0002t0001g0003a0001c0002t0001g0006others(208): Show | 224 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.2148+631A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992605 | ||||||
chr8:21992958
|
A | G | 1 | a0001c0002t0001g0234 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2148+984A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21992958 | ||||||
chr8:21993019
|
A | G | 1 | a0001c0003t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2148+1045A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993019 | ||||||
chr8:21993145
|
A | G | 94 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(91): Show | 102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.2148+1171A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993145 | ||||||
chr8:21993147
|
CTT | C | 23 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0306others(20): Show | 25 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.2148+1175_2148+117 others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993147 | |||||
chr8:21993176
|
G | A | 108 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(105): Show | 112 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.2149-1187G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993176 | ||||||
chr8:21993194
|
G | T | 1 | a0001c0003t0001g0121 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2149-1169G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993194 | ||||||
chr8:21993201
|
A | C | 1 | a0001c0001t0002g0186 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2149-1162A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993201 | ||||||
chr8:21993590
|
G | A | 5 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149-773G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993590 | ||||||
chr8:21993616
|
T | C | 1 | a0001c0003t0001g0031 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2149-747T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993616 | ||||||
chr8:21993915
|
G | GTC | 58 | a0001c0001t0002g0317a0001c0002t0001g0003a0001c0002t0001g0022others(55): Show | 62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.2149-424_2149-423d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993915 | |||||
chr8:21993915
|
G | GTCTC | 9 | a0001c0001t0002g0010a0001c0002t0001g0012a0001c0002t0001g0013others(6): Show | 12 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2149-426_2149-423d others(6): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993915 | |||||
chr8:21993915
|
G | GTCTCTC | 3 | a0001c0002t0001g0267a0001c0002t0001g0286a0001c0002t0001g0287 | 3 | HG02258.hp1 NA18955.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2149-428_2149-423d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr8 | 21993915 | |||||
chr8:21993997
|
G | A | 1 | a0001c0004t0001g0296 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2149-366G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21993997 | ||||||
chr8:21994016
|
C | T | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2149-347C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994016 | ||||||
chr8:21994064
|
C | G | 1 | a0001c0002t0001g0293 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2149-299C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994064 | ||||||
chr8:21994283
|
A | C | 1 | a0001c0003t0012g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2149-80A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994283 | ||||||
chr8:21994322
|
T | A | 1 | a0001c0003t0003g0094 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2149-41T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 19/27 | chr8 | 21994322 | ||||||
chr8:21994738
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2237+287G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21994738 | ||||||
chr8:21995064
|
AAATAAT | A | 94 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(91): Show | 102 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.2238-410_2238-405d others(8): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr8 | 21995064 | |||||
chr8:21995070
|
T | A | 1 | a0001c0002t0005g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2238-422T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995070 | ||||||
chr8:21995122
|
G | A | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2238-370G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995122 | ||||||
chr8:21995176
|
T | C | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2238-316T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995176 | ||||||
chr8:21995200
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2238-292T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995200 | ||||||
chr8:21995206
|
A | T | 1 | a0001c0002t0001g0024 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2238-286A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995206 | ||||||
chr8:21995300
|
C | G | 8 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0001g0233others(5): Show | 8 | NA18949.hp2 NA18970.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.2238-192C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995300 | ||||||
chr8:21995368
|
A | C | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2238-124A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 20/27 | chr8 | 21995368 | ||||||
chr8:21995780
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2345+181T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21995780 | ||||||
chr8:21995917
|
G | A | 2 | a0001c0002t0001g0252a0003c0012t0001g0251 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2345+318G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21995917 | ||||||
chr8:21995940
|
G | A | 2 | a0001c0002t0001g0257a0001c0003t0001g0044 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2345+341G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21995940 | ||||||
chr8:21996109
|
C | T | 4 | a0001c0002t0001g0306a0001c0002t0001g0307a0001c0002t0001g0308others(1): Show | 4 | HG01358.hp1 HG01928.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.2345+510C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996109 | ||||||
chr8:21996222
|
T | C | 85 | a0001c0003t0001g0002a0001c0003t0001g0004a0001c0003t0001g0031others(82): Show | 88 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2345+623T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996222 | ||||||
chr8:21996559
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2345+960T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996559 | ||||||
chr8:21996677
|
T | A | 179 | a0001c0002t0001g0003a0001c0002t0001g0012a0001c0002t0001g0013others(176): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.2345+1078T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996677 | ||||||
chr8:21996966
|
G | A | 85 | a0001c0003t0001g0002a0001c0003t0001g0004a0001c0003t0001g0031others(82): Show | 88 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2345+1367G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21996966 | ||||||
chr8:21997014
|
G | T | 1 | a0001c0002t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2345+1415G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997014 | ||||||
chr8:21997061
|
G | T | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2345+1462G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997061 | ||||||
chr8:21997149
|
T | C | 3 | a0001c0002t0006g0318a0001c0002t0006g0319a0001c0002t0006g0320 | 3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2345+1550T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997149 | ||||||
chr8:21997203
|
A | C | 1 | a0001c0002t0001g0279 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2346-1552A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997203 | ||||||
chr8:21997208
|
A | C | 1 | a0001c0003t0003g0094 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2346-1547A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997208 | ||||||
chr8:21997384
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2346-1371G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997384 | ||||||
chr8:21997514
|
G | A | 1 | a0001c0003t0001g0032 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2346-1241G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997514 | ||||||
chr8:21997613
|
C | G | 2 | a0001c0006t0005g0264a0001c0006t0005g0269 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2346-1142C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997613 | ||||||
chr8:21997784
|
G | C | 1 | a0001c0001t0002g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2346-971G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997784 | ||||||
chr8:21997846
|
G | T | 1 | a0001c0002t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2346-909G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997846 | ||||||
chr8:21997847
|
G | C | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0004g0290others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2346-908G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997847 | ||||||
chr8:21997889
|
C | A | 1 | a0001c0001t0002g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2346-866C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21997889 | ||||||
chr8:21998042
|
A | G | 1 | a0001c0002t0005g0261 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2346-713A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998042 | ||||||
chr8:21998169
|
C | T | 10 | a0001c0002t0001g0158a0001c0002t0001g0159a0001c0002t0001g0160others(7): Show | 11 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2346-586C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998169 | ||||||
chr8:21998213
|
G | A | 1 | a0001c0005t0002g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2346-542G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998213 | ||||||
chr8:21998269
|
A | G | 208 | a0001c0001t0002g0010a0001c0002t0001g0003a0001c0002t0001g0006others(205): Show | 221 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.2346-486A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998269 | ||||||
chr8:21998309
|
C | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0211 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2346-446C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998309 | ||||||
chr8:21998310
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0218 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2346-445G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998310 | ||||||
chr8:21998398
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2346-357G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998398 | ||||||
chr8:21998752
|
C | T | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | splice_region_variant&intron_variant | LOW | c.2346-3C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 21/27 | chr8 | 21998752 | ||||||
chr8:21998866
|
G | T | 3 | a0001c0002t0005g0258a0001c0002t0005g0265a0001c0002t0005g0294 | 3 | HG03195.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2428+29G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21998866 | ||||||
chr8:21998894
|
T | C | 3 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0004g0290 | 3 | HG02451.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2428+57T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21998894 | ||||||
chr8:21999043
|
G | C | 5 | a0001c0003t0003g0070a0001c0003t0003g0087a0001c0003t0003g0094others(2): Show | 5 | NA18942.hp1 NA18950.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2429-48G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21999043 | ||||||
chr8:21999046
|
C | T | 4 | a0001c0001t0002g0123a0001c0001t0002g0213a0001c0001t0002g0214others(1): Show | 4 | NA19000.hp1 NA19005.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.2429-45C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21999046 | ||||||
chr8:21999052
|
T | C | 5 | a0001c0003t0003g0070a0001c0003t0003g0087a0001c0003t0003g0094others(2): Show | 5 | NA18942.hp1 NA18950.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2429-39T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 22/27 | chr8 | 21999052 | ||||||
chr8:21999500
|
G | C | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2644-36G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 23/27 | chr8 | 21999500 | ||||||
chr8:21999756
|
G | A | 106 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(103): Show | 110 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2782+82G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 21999756 | ||||||
chr8:21999872
|
T | A | 1 | a0001c0007t0001g0315 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2782+198T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 21999872 | ||||||
chr8:22000068
|
A | G | 2 | a0001c0006t0005g0264a0001c0006t0005g0269 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2782+394A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000068 | ||||||
chr8:22000097
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2782+423G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000097 | ||||||
chr8:22000104
|
A | G | 1 | a0001c0002t0005g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2782+430A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000104 | ||||||
chr8:22000276
|
G | A | 107 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(104): Show | 111 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2782+602G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000276 | ||||||
chr8:22000280
|
A | C | 1 | a0001c0002t0006g0320 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2782+606A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000280 | ||||||
chr8:22000386
|
A | G | 1 | a0001c0003t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2782+712A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000386 | ||||||
chr8:22000440
|
C | T | 2 | a0001c0002t0001g0252a0003c0012t0001g0251 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2782+766C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000440 | ||||||
chr8:22000453
|
A | AT | 74 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(71): Show | 80 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.2782+798dupT | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr8 | 22000453 | |||||
chr8:22000453
|
A | ATT | 101 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(98): Show | 105 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2782+797_2782+798d others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr8 | 22000453 | |||||
chr8:22000483
|
C | A | 5 | a0001c0003t0001g0043a0001c0003t0001g0044a0001c0003t0001g0045others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2782+809C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000483 | ||||||
chr8:22000565
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2782+891G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000565 | ||||||
chr8:22000805
|
A | C | 4 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0252others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2782+1131A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000805 | ||||||
chr8:22000829
|
G | A | 323 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(320): Show | 340 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.2782+1155G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22000829 | ||||||
chr8:22001108
|
C | T | 204 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(201): Show | 216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2783-1004C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001108 | ||||||
chr8:22001164
|
G | C | 1 | a0001c0001t0002g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2783-948G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001164 | ||||||
chr8:22001284
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2783-828G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001284 | ||||||
chr8:22001287
|
C | T | 5 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2783-825C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001287 | ||||||
chr8:22001343
|
G | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2783-769G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001343 | ||||||
chr8:22001360
|
A | G | 1 | a0001c0003t0002g0295 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2783-752A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001360 | ||||||
chr8:22001378
|
A | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2783-734A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001378 | ||||||
chr8:22001455
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2783-657G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001455 | ||||||
chr8:22001532
|
T | C | 1 | a0001c0002t0004g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2783-580T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001532 | ||||||
chr8:22001557
|
A | G | 1 | a0001c0003t0001g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2783-555A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001557 | ||||||
chr8:22001573
|
G | A | 205 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(202): Show | 217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2783-539G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001573 | ||||||
chr8:22001583
|
A | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2783-529A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001583 | ||||||
chr8:22001606
|
C | G | 1 | a0001c0002t0002g0250 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2783-506C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001606 | ||||||
chr8:22001695
|
T | C | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2783-417T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001695 | ||||||
chr8:22001705
|
C | CTCCTAAT | 2 | a0001c0001t0002g0010a0001c0001t0002g0167 | 3 | HG00738.hp1 HG01099.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2783-404_2783-398d others(9): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr8 | 22001705 | |||||
chr8:22001804
|
C | T | 206 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(203): Show | 218 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.2783-308C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001804 | ||||||
chr8:22001934
|
A | T | 3 | a0001c0003t0001g0048a0001c0003t0001g0056a0001c0003t0001g0057 | 3 | HG01109.hp1 HG01261.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2783-178A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001934 | ||||||
chr8:22001974
|
G | A | 107 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(104): Show | 111 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2783-138G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22001974 | ||||||
chr8:22002044
|
A | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0009g0270 | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2783-68A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22002044 | ||||||
chr8:22002088
|
T | A | 1 | a0001c0005t0002g0148 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2783-24T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 24/27 | chr8 | 22002088 | ||||||
chr8:22002313
|
G | A | 2 | a0001c0002t0001g0252a0003c0012t0001g0251 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2943+41G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002313 | ||||||
chr8:22002396
|
G | A | 4 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(1): Show | 4 | HG00323.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2943+124G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002396 | ||||||
chr8:22002477
|
C | A | 1 | a0001c0003t0001g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2943+205C>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002477 | ||||||
chr8:22002480
|
C | T | 107 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(104): Show | 111 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2943+208C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002480 | ||||||
chr8:22002488
|
C | T | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2943+216C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002488 | ||||||
chr8:22002496
|
T | C | 205 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(202): Show | 217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2943+224T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002496 | ||||||
chr8:22002539
|
G | T | 1 | a0001c0002t0001g0284 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2943+267G>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002539 | ||||||
chr8:22002574
|
G | A | 1 | a0001c0003t0001g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2943+302G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002574 | ||||||
chr8:22002631
|
GGAA | G | 5 | a0001c0003t0001g0043a0001c0003t0001g0044a0001c0003t0001g0045others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2943+366_2943+368d others(5): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr8 | 22002631 | |||||
chr8:22002797
|
T | TAA | 95 | a0001c0001t0002g0226a0001c0002t0001g0003a0001c0002t0001g0012others(92): Show | 103 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.2944-421_2944-420i others(4): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr8 | 22002797 | |||||
chr8:22002914
|
T | A | 107 | a0001c0002t0001g0006a0001c0002t0001g0155a0001c0002t0001g0229others(104): Show | 111 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2944-305T>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002914 | ||||||
chr8:22002922
|
A | C | 1 | a0001c0001t0002g0197 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2944-297A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002922 | ||||||
chr8:22002922
|
A | G | 1 | a0001c0001t0002g0127 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2944-297A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22002922 | ||||||
chr8:22003135
|
A | G | 1 | a0001c0002t0004g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2944-84A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22003135 | ||||||
chr8:22003160
|
T | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02622.hp2 HG02717.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2944-59T>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 25/27 | chr8 | 22003160 | ||||||
chr8:22003335
|
C | T | 1 | a0001c0002t0001g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3042+18C>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003335 | ||||||
chr8:22003383
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3042+66G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003383 | ||||||
chr8:22003392
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3042+75G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003392 | ||||||
chr8:22003701
|
A | G | 1 | a0001c0003t0001g0118 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3043-202A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 26/27 | chr8 | 22003701 | ||||||
chr8:22004152
|
G | C | 201 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0012others(198): Show | 213 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.3170+122G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004152 | ||||||
chr8:22004376
|
T | C | 8 | a0001c0002t0001g0003a0001c0002t0001g0022a0001c0002t0001g0023others(5): Show | 9 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3170+346T>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004376 | ||||||
chr8:22004430
|
A | T | 1 | a0001c0003t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3170+400A>T | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004430 | ||||||
chr8:22004511
|
A | C | 2 | a0001c0002t0001g0255a0001c0002t0001g0256 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3170+481A>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004511 | ||||||
chr8:22004621
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3171-374G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004621 | ||||||
chr8:22004637
|
G | A | 1 | a0001c0002t0005g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3171-358G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004637 | ||||||
chr8:22004640
|
G | C | 7 | a0001c0002t0005g0258a0001c0002t0005g0261a0001c0002t0005g0265others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3171-355G>C | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004640 | ||||||
chr8:22004733
|
G | A | 1 | a0001c0002t0001g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3171-262G>A | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004733 | ||||||
chr8:22004919
|
TA | T | 105 | a0001c0001t0002g0168a0001c0001t0002g0200a0001c0002t0001g0006others(102): Show | 109 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.3171-58delA | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr8 | 22004919 | |||||
chr8:22004919
|
TAA | T | 6 | a0001c0002t0001g0046a0001c0002t0001g0064a0001c0002t0001g0065others(3): Show | 6 | HG00735.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3171-59_3171-58del others(2): Show |
XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr8 | 22004919 | |||||
chr8:22004945
|
A | G | 1 | a0001c0001t0002g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3171-50A>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004945 | ||||||
chr8:22004957
|
C | G | 1 | a0001c0001t0002g0021 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3171-38C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004957 | ||||||
chr8:22004969
|
C | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0199 | 2 | HG00621.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.3171-26C>G | XPO7 | ENSG00000130227.17 | transcript | ENST00000252512.14 | protein_coding | 27/27 | chr8 | 22004969 |