geneid | 1969 |
---|---|
ensemblid | ENSG00000142627.13 |
hgncid | 3386 |
symbol | EPHA2 |
name | EPH receptor A2 |
refseq_nuc | NM_004431.5 |
refseq_prot | NP_004422.2 |
ensembl_nuc | ENST00000358432.8 |
ensembl_prot | ENSP00000351209.5 |
mane_status | MANE Select |
chr | chr1 |
start | 16124337 |
end | 16156069 |
strand | - |
ver | v1.2 |
region | chr1:16124337-16156069 |
region5000 | chr1:16119337-16161069 |
regionname0 | EPHA2_chr1_16124337_16156069 |
regionname5000 | EPHA2_chr1_16119337_16161069 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 976 | 283 | 77 | 60 | 88 | 16 | 40 | 58 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0002 | 0/0 | 976 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0003 | 0/0 | 976 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0004 | 0/0 | 976 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0005 | 0/0 | 976 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0006 | 0/0 | 976 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0007 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0008 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0009 | 0/0 | 976 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0010 | 0/0 | 976 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0011 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0012 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0013 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2931 | 116 | 7 | 28 | 58 | 4 | 18 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0002 | 0/0 | 2931 | 33 | 12 | 8 | 11 | 1 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0003 | 0/1 | 2931 | 30 | 6 | 4 | 11 | 2 | 6 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0004 | 0/0 | 2931 | 29 | 26 | 1 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0005 | 0/0 | 2931 | 24 | 13 | 4 | 0 | 3 | 4 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0006 | 0/0 | 2931 | 20 | 0 | 5 | 5 | 3 | 7 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0007 | 0/0 | 2931 | 7 | 0 | 7 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0008 | 0/0 | 2931 | 7 | 7 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0009 | 0/0 | 2931 | 6 | 2 | 4 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0010 | 0/0 | 2931 | 4 | 1 | 1 | 1 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0011 | 0/0 | 2931 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0012 | 0/0 | 2931 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0013 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0014 | 0/0 | 2931 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0015 | 0/0 | 2931 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0016 | 0/0 | 2931 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0017 | 0/0 | 2931 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0018 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0019 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0020 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0021 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0022 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0023 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0024 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0025 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0026 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0027 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0028 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0029 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0030 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0031 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0032 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0033 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0034 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0035 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
c0036 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1016 | 266 | 71 | 65 | 73 | 16 | 40 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
t0002 | 1/0 | 1016 | 29 | 9 | 4 | 13 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
t0003 | 0/0 | 1016 | 11 | 11 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
t0004 | 0/0 | 1016 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
t0005 | 0/0 | 1016 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
t0006 | 0/0 | 1016 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
t0007 | 0/0 | 1016 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 5 | 1 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0004 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0027 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2931 | 116 | 7 | 28 | 58 | 4 | 18 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0002 | 0/0 | 2931 | 33 | 12 | 8 | 11 | 1 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0003 | 0/1 | 2931 | 30 | 6 | 4 | 11 | 2 | 6 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0004 | 0/0 | 2931 | 29 | 26 | 1 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0005 | 0/0 | 2931 | 24 | 13 | 4 | 0 | 3 | 4 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0006 | 0/0 | 2931 | 20 | 0 | 5 | 5 | 3 | 7 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0009 | 0/0 | 2931 | 6 | 2 | 4 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0010 | 0/0 | 2931 | 4 | 1 | 1 | 1 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0012 | 0/0 | 2931 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0014 | 0/0 | 2931 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0015 | 0/0 | 2931 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0016 | 0/0 | 2931 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0018 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0023 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0024 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0026 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0027 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0030 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0031 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0032 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0033 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0034 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0036 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0002c0008 | 0/0 | 2931 | 7 | 7 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0002c0035 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0003c0007 | 0/0 | 2931 | 7 | 0 | 7 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0004c0011 | 0/0 | 2931 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0005c0017 | 0/0 | 2931 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0006c0013 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0007c0019 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0008c0020 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0009c0028 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0010c0025 | 0/0 | 2931 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0011c0022 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0012c0021 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0013c0029 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3946 | 104 | 7 | 27 | 50 | 4 | 16 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0001t0002 | 1/0 | 3946 | 11 | 0 | 1 | 7 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0001t0006 | 0/0 | 3946 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0002t0001 | 0/0 | 3946 | 20 | 10 | 5 | 3 | 1 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0002t0002 | 0/0 | 3946 | 10 | 2 | 3 | 5 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0002t0004 | 0/0 | 3946 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0003t0001 | 0/1 | 3946 | 30 | 6 | 4 | 11 | 2 | 6 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0004t0001 | 0/0 | 3946 | 24 | 21 | 1 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0004t0002 | 0/0 | 3946 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0005t0001 | 0/0 | 3946 | 23 | 12 | 4 | 0 | 3 | 4 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0005t0007 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0006t0001 | 0/0 | 3946 | 20 | 0 | 5 | 5 | 3 | 7 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0009t0001 | 0/0 | 3946 | 6 | 2 | 4 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0010t0001 | 0/0 | 3946 | 4 | 1 | 1 | 1 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0012t0001 | 0/0 | 3946 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0014t0001 | 0/0 | 3946 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0015t0001 | 0/0 | 3946 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0016t0001 | 0/0 | 3946 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0018t0002 | 0/0 | 3946 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0023t0002 | 0/0 | 3946 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0024t0003 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0026t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0027t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0030t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0031t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0032t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0033t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0034t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0001c0036t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0002c0008t0003 | 0/0 | 3946 | 7 | 7 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0002c0035t0003 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0003c0007t0001 | 0/0 | 3946 | 6 | 0 | 6 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0003c0007t0005 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0004c0011t0001 | 0/0 | 3946 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0005c0017t0001 | 0/0 | 3946 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0006c0013t0003 | 0/0 | 3946 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0007c0019t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0008c0020t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0009c0028t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0010c0025t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0011c0022t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0012c0021t0001 | 0/0 | 3946 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
a0013c0029t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | copy fasta | chr1 | 16119337 | 16161069 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 5 | 1 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0027 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0004t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0004 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0005t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0009t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0009t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0009t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0009t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0010t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0010t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0010t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0010t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0012t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0012t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0014t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0014t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0015t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0015t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0016t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0018t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0018t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0023t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0024t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0026t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0027t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0030t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0031t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0032t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0033t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0034t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0001c0036t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0008t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0008t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0008t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0008t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0008t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0008t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0008t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0002c0035t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0003c0007t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0003c0007t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0003c0007t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0003c0007t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0003c0007t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0004c0011t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0004c0011t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0004c0011t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0005c0017t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0005c0017t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0006c0013t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0006c0013t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0007c0019t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0008c0020t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0009c0028t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0010c0025t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0011c0022t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0012c0021t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
a0013c0029t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0027 | EUR | GBR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00099 | hp2 | a0001 | c0006 | t0001 | g0017 | EUR | GBR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00323 | hp1 | a0001 | c0006 | t0001 | g0147 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0176 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00609 | hp2 | a0001 | c0002 | t0004 | g0093 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00621 | hp1 | a0001 | c0002 | t0004 | g0227 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00639 | hp2 | a0001 | c0009 | t0001 | g0248 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00642 | hp2 | a0001 | c0004 | t0001 | g0030 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00673 | hp1 | a0005 | c0017 | t0001 | g0057 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00733 | hp1 | a0001 | c0006 | t0001 | g0151 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00735 | hp2 | a0011 | c0022 | t0001 | g0274 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00738 | hp2 | a0001 | c0009 | t0001 | g0005 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00741 | hp1 | a0008 | c0020 | t0001 | g0234 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01069 | hp2 | a0001 | c0006 | t0001 | g0085 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01071 | hp1 | a0001 | c0005 | t0001 | g0138 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01081 | hp1 | a0003 | c0007 | t0005 | g0029 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0219 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01109 | hp2 | a0001 | c0012 | t0001 | g0018 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01168 | hp2 | a0001 | c0006 | t0001 | g0016 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01169 | hp2 | a0001 | c0006 | t0001 | g0016 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01192 | hp1 | a0005 | c0017 | t0001 | g0221 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01192 | hp2 | a0001 | c0005 | t0001 | g0148 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01243 | hp2 | a0001 | c0034 | t0001 | g0273 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0209 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01257 | hp2 | a0001 | c0009 | t0001 | g0223 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01261 | hp2 | a0001 | c0014 | t0001 | g0130 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01361 | hp2 | a0003 | c0007 | t0001 | g0132 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0090 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01433 | hp2 | a0003 | c0007 | t0001 | g0003 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01496 | hp2 | a0001 | c0009 | t0001 | g0005 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01515 | hp1 | a0001 | c0016 | t0001 | g0013 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01515 | hp2 | a0001 | c0005 | t0001 | g0143 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01516 | hp1 | a0001 | c0031 | t0001 | g0156 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01516 | hp2 | a0001 | c0005 | t0001 | g0004 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01517 | hp1 | a0001 | c0016 | t0001 | g0013 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01517 | hp2 | a0001 | c0005 | t0001 | g0004 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0270 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01891 | hp1 | a0013 | c0029 | t0001 | g0119 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01928 | hp2 | a0001 | c0030 | t0001 | g0157 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0208 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01943 | hp2 | a0003 | c0007 | t0001 | g0124 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01952 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01975 | hp1 | a0001 | c0010 | t0001 | g0066 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01975 | hp2 | a0001 | c0005 | t0001 | g0141 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01978 | hp1 | a0003 | c0007 | t0001 | g0003 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01978 | hp2 | a0001 | c0005 | t0001 | g0137 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01993 | hp1 | a0003 | c0007 | t0001 | g0133 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02083 | hp1 | a0012 | c0021 | t0001 | g0235 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02129 | hp1 | a0001 | c0023 | t0002 | g0129 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02135 | hp2 | a0001 | c0003 | t0001 | g0245 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02145 | hp1 | a0001 | c0024 | t0003 | g0082 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02145 | hp2 | a0001 | c0027 | t0001 | g0251 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | CDX | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02257 | hp1 | a0004 | c0011 | t0001 | g0262 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0266 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0217 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02293 | hp2 | a0003 | c0007 | t0001 | g0003 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02300 | hp1 | a0001 | c0015 | t0001 | g0253 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02300 | hp2 | a0001 | c0006 | t0001 | g0017 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02572 | hp2 | a0002 | c0008 | t0003 | g0111 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0084 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02615 | hp2 | a0001 | c0012 | t0001 | g0018 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0028 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02630 | hp1 | a0001 | c0015 | t0001 | g0231 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0269 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02683 | hp2 | a0001 | c0005 | t0001 | g0145 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0201 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02698 | hp2 | a0009 | c0028 | t0001 | g0122 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02717 | hp1 | a0002 | c0008 | t0003 | g0117 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0247 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02723 | hp1 | a0001 | c0004 | t0002 | g0113 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0258 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02735 | hp1 | a0001 | c0006 | t0001 | g0142 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02735 | hp2 | a0001 | c0006 | t0001 | g0123 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02738 | hp2 | a0001 | c0005 | t0001 | g0140 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02809 | hp2 | a0001 | c0004 | t0001 | g0161 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02818 | hp1 | a0001 | c0018 | t0002 | g0228 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02818 | hp2 | a0001 | c0005 | t0001 | g0144 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0265 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02895 | hp1 | a0002 | c0008 | t0003 | g0271 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0154 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0023 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02897 | hp1 | a0002 | c0008 | t0003 | g0257 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0023 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02922 | hp1 | a0001 | c0004 | t0002 | g0087 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02922 | hp2 | a0001 | c0036 | t0001 | g0115 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0158 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0216 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02970 | hp2 | a0002 | c0008 | t0003 | g0118 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02976 | hp1 | a0001 | c0012 | t0001 | g0163 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02976 | hp2 | a0001 | c0032 | t0001 | g0032 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03017 | hp1 | a0001 | c0006 | t0001 | g0083 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0198 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03041 | hp1 | a0002 | c0008 | t0003 | g0110 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03041 | hp2 | a0001 | c0009 | t0001 | g0005 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0136 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0215 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03130 | hp1 | a0007 | c0019 | t0001 | g0255 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03130 | hp2 | a0006 | c0013 | t0003 | g0128 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0187 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0267 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03195 | hp2 | a0001 | c0005 | t0001 | g0160 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03209 | hp1 | a0001 | c0004 | t0002 | g0114 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03225 | hp1 | a0002 | c0035 | t0003 | g0252 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03239 | hp2 | a0001 | c0006 | t0001 | g0153 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0194 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03486 | hp1 | a0001 | c0018 | t0002 | g0229 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03490 | hp2 | a0001 | c0005 | t0001 | g0014 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03491 | hp2 | a0001 | c0006 | t0001 | g0126 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03492 | hp1 | a0001 | c0005 | t0001 | g0014 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03540 | hp1 | a0002 | c0008 | t0003 | g0109 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03540 | hp2 | a0001 | c0004 | t0002 | g0108 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03579 | hp2 | a0004 | c0011 | t0001 | g0263 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03654 | hp1 | a0001 | c0033 | t0001 | g0098 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03654 | hp2 | a0001 | c0010 | t0001 | g0203 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03831 | hp1 | a0001 | c0004 | t0001 | g0211 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0200 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03834 | hp1 | a0001 | c0006 | t0001 | g0155 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0199 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG04204 | hp1 | a0001 | c0006 | t0001 | g0121 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18522 | hp1 | a0001 | c0005 | t0001 | g0134 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18522 | hp2 | a0004 | c0011 | t0001 | g0264 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CHB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0261 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0218 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18951 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18965 | hp1 | a0001 | c0006 | t0001 | g0152 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18973 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18990 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18998 | hp2 | a0001 | c0006 | t0001 | g0150 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA18999 | hp2 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19001 | hp2 | a0001 | c0006 | t0001 | g0120 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19004 | hp2 | a0001 | c0006 | t0001 | g0149 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19011 | hp2 | a0001 | c0014 | t0001 | g0131 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19030 | hp1 | a0001 | c0026 | t0001 | g0159 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19043 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0233 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19065 | hp1 | a0001 | c0010 | t0001 | g0060 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0031 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ASW | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20129 | hp2 | a0001 | c0010 | t0001 | g0190 | AFR | ASW | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0167 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20805 | hp2 | a0001 | c0006 | t0001 | g0146 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20905 | hp1 | a0010 | c0025 | t0001 | g0125 | SAS | GIH | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02109 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02109 | hp2 | a0001 | c0004 | t0001 | g0260 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02486 | hp2 | a0001 | c0005 | t0001 | g0139 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02559 | hp1 | a0001 | c0005 | t0007 | g0127 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG02559 | hp2 | a0001 | c0009 | t0001 | g0249 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG03471 | hp2 | a0001 | c0004 | t0002 | g0112 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG06807 | hp1 | a0001 | c0005 | t0001 | g0135 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
HG06807 | hp2 | a0006 | c0013 | t0003 | g0077 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0107 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA21309 | hp1 | a0001 | c0004 | t0001 | g0250 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0028 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0027 | REF | REF | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0095 | REF | REF | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:16125271
|
C | T | 1 | a0011 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.2875G>A | p.Ala959Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 3012/3946 | 2875/2931 | 959/976 | chr1 | 16125271 | ||
chr1:16131741
|
A | C | 1 | a0010 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2455T>G | p.Trp819Gly | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/17 | 2592/3946 | 2455/2931 | 819/976 | chr1 | 16131741 | ||
chr1:16133341
|
A | G | 2 | a0002a0006 | 10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
missense_variant | MODERATE | c.1892T>C | p.Met631Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2029/3946 | 1892/2931 | 631/976 | chr1 | 16133341 | ||
chr1:16134529
|
C | T | 1 | a0004 | 3 | HG02257.hp1 HG03579.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.1621G>A | p.Val541Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/17 | 1758/3946 | 1621/2931 | 541/976 | chr1 | 16134529 | ||
chr1:16135086
|
G | A | 1 | a0005 | 2 | HG00673.hp1 HG01192.hp1 |
missense_variant | MODERATE | c.1532C>T | p.Thr511Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1669/3946 | 1532/2931 | 511/976 | chr1 | 16135086 | ||
chr1:16135132
|
C | T | 1 | a0006 | 2 | HG03130.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.1486G>A | p.Asp496Asn | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1623/3946 | 1486/2931 | 496/976 | chr1 | 16135132 | ||
chr1:16135176
|
C | G | 1 | a0012 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.1442G>C | p.Ser481Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1579/3946 | 1442/2931 | 481/976 | chr1 | 16135176 | ||
chr1:16137994
|
C | T | 2 | a0003a0008 | 8 | HG00741.hp1 HG01081.hp1 HG01361.hp2 others(5): Show |
missense_variant | MODERATE | c.1171G>A | p.Gly391Arg | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/17 | 1308/3946 | 1171/2931 | 391/976 | chr1 | 16137994 | ||
chr1:16138119
|
G | A | 1 | a0009 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1046C>T | p.Thr349Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/17 | 1183/3946 | 1046/2931 | 349/976 | chr1 | 16138119 | ||
chr1:16138310
|
C | T | 1 | a0008 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.944G>A | p.Arg315Gln | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 4/17 | 1081/3946 | 944/2931 | 315/976 | chr1 | 16138310 | ||
chr1:16148506
|
T | C | 1 | a0013 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.695A>G | p.Asp232Gly | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 832/3946 | 695/2931 | 232/976 | chr1 | 16148506 | ||
chr1:16148708
|
C | T | 1 | a0007 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.493G>A | p.Val165Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 630/3946 | 493/2931 | 165/976 | chr1 | 16148708 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:16125227
|
C | T | 1 | a0001c0009 | 6 | HG00639.hp2 HG00738.hp2 HG01257.hp2 others(3): Show |
synonymous_variant | LOW | c.2919G>A | p.Gly973Gly | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 3056/3946 | 2919/2931 | 973/976 | chr1 | 16125227 | ||
chr1:16125272
|
G | A | 15 | a0001c0003a0001c0006a0001c0010others(12): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(72): Show |
synonymous_variant | LOW | c.2874C>T | p.Ile958Ile | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 3011/3946 | 2874/2931 | 958/976 | chr1 | 16125272 | ||
chr1:16130303
|
G | A | 1 | a0001c0032 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2592C>T | p.Phe864Phe | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/17 | 2729/3946 | 2592/2931 | 864/976 | chr1 | 16130303 | ||
chr1:16130381
|
T | C | 4 | a0001c0024a0002c0008a0002c0035others(1): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
synonymous_variant | LOW | c.2514A>G | p.Thr838Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/17 | 2651/3946 | 2514/2931 | 838/976 | chr1 | 16130381 | ||
chr1:16133199
|
T | C | 7 | a0001c0012a0001c0024a0001c0027others(4): Show | 16 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.2034A>G | p.Leu678Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2171/3946 | 2034/2931 | 678/976 | chr1 | 16133199 | ||
chr1:16133250
|
G | A | 12 | a0001c0003a0001c0004a0001c0012others(9): Show | 75 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(72): Show |
synonymous_variant | LOW | c.1983C>T | p.Leu661Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2120/3946 | 1983/2931 | 661/976 | chr1 | 16133250 | ||
chr1:16133292
|
C | A | 1 | a0001c0016 | 2 | HG01515.hp1 HG01517.hp1 |
synonymous_variant | LOW | c.1941G>T | p.Thr647Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2078/3946 | 1941/2931 | 647/976 | chr1 | 16133292 | ||
chr1:16135106
|
C | A | 4 | a0001c0036a0002c0008a0002c0035others(1): Show | 11 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(8): Show |
synonymous_variant | LOW | c.1512G>T | p.Leu504Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1649/3946 | 1512/2931 | 504/976 | chr1 | 16135106 | ||
chr1:16138178
|
G | A | 19 | a0001c0002a0001c0005a0001c0006others(16): Show | 108 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
synonymous_variant | LOW | c.987C>T | p.Pro329Pro | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/17 | 1124/3946 | 987/2931 | 329/976 | chr1 | 16138178 | ||
chr1:16148553
|
G | A | 2 | a0001c0030a0001c0031 | 2 | HG01516.hp1 HG01928.hp2 |
synonymous_variant | LOW | c.648C>T | p.Ala216Ala | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 785/3946 | 648/2931 | 216/976 | chr1 | 16148553 | ||
chr1:16148628
|
C | T | 20 | a0001c0005a0001c0006a0001c0009others(17): Show | 77 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(74): Show |
synonymous_variant | LOW | c.573G>A | p.Leu191Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 710/3946 | 573/2931 | 191/976 | chr1 | 16148628 | ||
chr1:16148631
|
C | T | 20 | a0001c0005a0001c0006a0001c0009others(17): Show | 77 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(74): Show |
synonymous_variant | LOW | c.570G>A | p.Ala190Ala | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 707/3946 | 570/2931 | 190/976 | chr1 | 16148631 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:16124473
|
A | T | 4 | a0001c0024t0003a0002c0008t0003a0002c0035t0003others(1): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*742T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 742 | chr1 | 16124473 | |||||
chr1:16124501
|
C | T | 4 | a0001c0024t0003a0002c0008t0003a0002c0035t0003others(1): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*714G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 714 | chr1 | 16124501 | |||||
chr1:16124556
|
A | T | 1 | a0001c0001t0006 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 659 | chr1 | 16124556 | |||||
chr1:16124705
|
C | T | 1 | a0001c0002t0004 | 3 | HG00609.hp2 HG00621.hp1 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*510G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 510 | chr1 | 16124705 | |||||
chr1:16124772
|
A | G | 4 | a0001c0024t0003a0002c0008t0003a0002c0035t0003others(1): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*443T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 443 | chr1 | 16124772 | |||||
chr1:16124888
|
G | C | 1 | a0001c0005t0007 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 327 | chr1 | 16124888 | |||||
chr1:16124918
|
C | T | 37 | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(34): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*297G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 297 | chr1 | 16124918 | |||||
chr1:16125049
|
C | T | 4 | a0001c0024t0003a0002c0008t0003a0002c0035t0003others(1): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*166G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 166 | chr1 | 16125049 | |||||
chr1:16155935
|
C | T | 1 | a0003c0007t0005 | 1 | HG01081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/17 | 3 | chr1 | 16155935 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:16125376
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0101 | 2 | NA18957.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2826-56C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125376 | ||||||
chr1:16125381
|
G | A | 13 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(10): Show | 14 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.2826-61C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125381 | ||||||
chr1:16125526
|
G | A | 1 | a0001c0004t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2826-206C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125526 | ||||||
chr1:16125561
|
C | T | 1 | a0001c0002t0002g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2826-241G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125561 | ||||||
chr1:16125562
|
G | A | 3 | a0001c0004t0001g0030a0001c0004t0001g0031a0011c0022t0001g0274 | 3 | HG00642.hp2 HG00735.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2826-242C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125562 | ||||||
chr1:16125706
|
A | G | 124 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0116others(121): Show | 138 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2826-386T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125706 | ||||||
chr1:16125799
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0193a0005c0017t0001g0221 | 3 | HG01192.hp1 HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2826-479G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125799 | ||||||
chr1:16125964
|
G | A | 1 | a0001c0004t0001g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2826-644C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125964 | ||||||
chr1:16126047
|
C | T | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2826-727G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126047 | ||||||
chr1:16126048
|
G | A | 3 | a0001c0012t0001g0018a0001c0012t0001g0163a0001c0027t0001g0251 | 4 | HG01109.hp2 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2826-728C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126048 | ||||||
chr1:16126115
|
G | T | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2826-795C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126115 | ||||||
chr1:16126163
|
G | T | 6 | a0001c0024t0003g0082a0002c0008t0003g0117a0002c0008t0003g0118others(3): Show | 6 | HG02145.hp1 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2826-843C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126163 | ||||||
chr1:16126260
|
G | A | 12 | a0001c0004t0001g0107a0001c0024t0003g0082a0002c0008t0003g0109others(9): Show | 12 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2826-940C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126260 | ||||||
chr1:16126341
|
T | A | 1 | a0001c0006t0001g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2826-1021A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126341 | ||||||
chr1:16126354
|
C | T | 6 | a0001c0005t0001g0135a0001c0005t0001g0136a0001c0005t0001g0138others(3): Show | 6 | HG01071.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2826-1034G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126354 | ||||||
chr1:16126474
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2826-1154G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126474 | ||||||
chr1:16126503
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.2826-1183G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126503 | ||||||
chr1:16126676
|
C | T | 89 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(86): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2826-1356G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126676 | ||||||
chr1:16126721
|
T | A | 89 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(86): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2826-1401A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126721 | ||||||
chr1:16126796
|
G | A | 1 | a0001c0004t0001g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2826-1476C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126796 | ||||||
chr1:16126890
|
C | A | 2 | a0001c0002t0002g0091a0001c0002t0002g0092 | 2 | HG01074.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2826-1570G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126890 | ||||||
chr1:16127069
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2826-1749C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127069 | ||||||
chr1:16127120
|
G | A | 1 | a0001c0024t0003g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2826-1800C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127120 | ||||||
chr1:16127176
|
C | T | 13 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(10): Show | 14 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2826-1856G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127176 | ||||||
chr1:16127343
|
G | T | 1 | a0001c0005t0001g0143 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2826-2023C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127343 | ||||||
chr1:16127457
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2825+1977C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127457 | ||||||
chr1:16127467
|
G | A | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+1967C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127467 | ||||||
chr1:16128339
|
G | C | 57 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(54): Show | 62 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.2825+1095C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128339 | ||||||
chr1:16128345
|
G | A | 2 | a0001c0004t0001g0233a0001c0004t0001g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2825+1089C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128345 | ||||||
chr1:16128411
|
G | A | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+1023C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128411 | ||||||
chr1:16128557
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(148): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2825+877G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128557 | ||||||
chr1:16128647
|
C | G | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+787G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128647 | ||||||
chr1:16128648
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.2825+786A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128648 | ||||||
chr1:16128840
|
C | T | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+594G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128840 | ||||||
chr1:16128879
|
G | C | 1 | a0002c0008t0003g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2825+555C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128879 | ||||||
chr1:16128933
|
T | A | 1 | a0001c0005t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2825+501A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128933 | ||||||
chr1:16129022
|
C | A | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+412G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129022 | ||||||
chr1:16129186
|
G | T | 1 | a0011c0022t0001g0274 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2825+248C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129186 | ||||||
chr1:16129324
|
A | G | 8 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0166others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.2825+110T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129324 | ||||||
chr1:16129364
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2825+70C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129364 | ||||||
chr1:16129367
|
G | A | 1 | a0001c0003t0001g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2825+67C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129367 | ||||||
chr1:16129660
|
C | T | 2 | a0001c0004t0001g0233a0001c0004t0001g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2670-71G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129660 | ||||||
chr1:16129669
|
G | T | 1 | a0001c0006t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2670-80C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129669 | ||||||
chr1:16129681
|
G | A | 67 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(64): Show | 73 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.2670-92C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129681 | ||||||
chr1:16129851
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0174a0001c0001t0001g0175 | 3 | HG02523.hp2 NA18980.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.2670-262C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129851 | ||||||
chr1:16129934
|
G | A | 1 | a0005c0017t0001g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2669+292C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129934 | ||||||
chr1:16130071
|
G | T | 1 | a0001c0004t0002g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2669+155C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16130071 | ||||||
chr1:16130094
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2669+132T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16130094 | ||||||
chr1:16130150
|
G | A | 1 | a0001c0005t0001g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2669+76C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16130150 | ||||||
chr1:16130536
|
G | A | 11 | a0001c0024t0003g0082a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476-117C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130536 | ||||||
chr1:16130614
|
G | A | 1 | a0002c0008t0003g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2476-195C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130614 | ||||||
chr1:16130614
|
G | C | 1 | a0001c0003t0001g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2476-195C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130614 | ||||||
chr1:16130631
|
C | CT | 11 | a0001c0001t0001g0040a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG00738.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476-213dupA | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130631 | ||||||
chr1:16130705
|
C | T | 2 | a0001c0005t0001g0148a0001c0006t0001g0016 | 3 | HG01168.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2476-286G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130705 | ||||||
chr1:16130749
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2476-330G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130749 | ||||||
chr1:16130804
|
A | T | 1 | a0001c0006t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2476-385T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130804 | ||||||
chr1:16130818
|
T | C | 10 | a0002c0008t0003g0109a0002c0008t0003g0110a0002c0008t0003g0111others(7): Show | 10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2476-399A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130818 | ||||||
chr1:16130997
|
C | T | 1 | a0001c0002t0004g0093 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2476-578G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130997 | ||||||
chr1:16131191
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2475+530A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131191 | ||||||
chr1:16131307
|
C | T | 1 | a0001c0005t0007g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2475+414G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131307 | ||||||
chr1:16131577
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2475+144A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131577 | ||||||
chr1:16131581
|
C | CA | 7 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0105others(4): Show | 7 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2475+139dupT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131581 | ||||||
chr1:16131594
|
T | A | 6 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0105others(3): Show | 6 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2475+127A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131594 | ||||||
chr1:16131689
|
C | T | 1 | a0001c0005t0007g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2475+32G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131689 | ||||||
chr1:16131690
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2475+31C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131690 | ||||||
chr1:16131692
|
A | G | 16 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0105others(13): Show | 16 | HG01106.hp1 HG01167.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.2475+29T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131692 | ||||||
chr1:16131919
|
A | G | 1 | a0001c0006t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2326-49T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 13/16 | chr1 | 16131919 | ||||||
chr1:16132016
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2325+48A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 13/16 | chr1 | 16132016 | ||||||
chr1:16132319
|
C | T | 48 | a0001c0003t0001g0002a0001c0003t0001g0027a0001c0003t0001g0167others(45): Show | 51 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.2116-46G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 12/16 | chr1 | 16132319 | ||||||
chr1:16132353
|
C | T | 10 | a0002c0008t0003g0109a0002c0008t0003g0110a0002c0008t0003g0111others(7): Show | 10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2115+25G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 12/16 | chr1 | 16132353 | ||||||
chr1:16132546
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2054-107C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132546 | ||||||
chr1:16132694
|
CAGGTGGG others(79): Show |
C | 1 | a0001c0002t0001g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2054-341_2054-256d others(88): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132694 | ||||||
chr1:16132748
|
GGGTGTAA others(122): Show |
G | 1 | a0001c0001t0001g0019 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2053+303_2054-310d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132748 | ||||||
chr1:16132834
|
G | A | 2 | a0001c0002t0001g0105a0001c0002t0001g0106 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2053+346C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132834 | ||||||
chr1:16132856
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2053+324C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132856 | ||||||
chr1:16132859
|
TG | T | 10 | a0002c0008t0003g0109a0002c0008t0003g0110a0002c0008t0003g0111others(7): Show | 10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2053+320delC | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132859 | ||||||
chr1:16132867
|
A | C | 1 | a0001c0003t0001g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2053+313T>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132867 | ||||||
chr1:16132883
|
AAGGAGGT others(122): Show |
A | 1 | a0001c0004t0001g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2053+168_2053+296d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132883 | ||||||
chr1:16132904
|
G | A | 1 | a0011c0022t0001g0274 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2053+276C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132904 | ||||||
chr1:16132929
|
G | GGTGGGTA others(115): Show |
10 | a0002c0008t0003g0109a0002c0008t0003g0110a0002c0008t0003g0111others(7): Show | 10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2053+250_2053+251i others(124): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132929 | ||||||
chr1:16133012
|
T | A | 100 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0116others(97): Show | 109 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.2053+168A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133012 | ||||||
chr1:16133101
|
G | A | 1 | a0001c0004t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2053+79C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133101 | ||||||
chr1:16133129
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2053+51G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133129 | ||||||
chr1:16133142
|
C | T | 15 | a0001c0004t0001g0006a0001c0004t0001g0023a0001c0004t0001g0028others(12): Show | 19 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2053+38G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133142 | ||||||
chr1:16133469
|
G | A | 3 | a0001c0002t0001g0034a0001c0002t0001g0232a0001c0002t0001g0265 | 3 | HG02886.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1864+12C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 10/16 | chr1 | 16133469 | ||||||
chr1:16133634
|
G | A | 1 | a0004c0011t0001g0262 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1739-28C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133634 | ||||||
chr1:16133723
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1739-117G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133723 | ||||||
chr1:16133744
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1738+116G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133744 | ||||||
chr1:16133818
|
G | T | 1 | a0011c0022t0001g0274 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1738+42C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133818 | ||||||
chr1:16133844
|
G | A | 81 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(78): Show | 90 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.1738+16C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133844 | ||||||
chr1:16134046
|
T | C | 98 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0116others(95): Show | 107 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.1683-131A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134046 | ||||||
chr1:16134080
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1683-165G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134080 | ||||||
chr1:16134081
|
G | A | 1 | a0001c0003t0001g0204 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1683-166C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134081 | ||||||
chr1:16134090
|
G | A | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1683-175C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134090 | ||||||
chr1:16134117
|
G | A | 3 | a0004c0011t0001g0262a0004c0011t0001g0263a0004c0011t0001g0264 | 3 | HG02257.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1683-202C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134117 | ||||||
chr1:16134201
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0070 | 3 | HG00642.hp1 HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1682+267C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134201 | ||||||
chr1:16134248
|
TAAC | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(264): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1682+217_1682+219d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134248 | ||||||
chr1:16134345
|
G | A | 80 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(77): Show | 89 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.1682+123C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134345 | ||||||
chr1:16134626
|
G | A | 15 | a0001c0004t0001g0006a0001c0004t0001g0023a0001c0004t0001g0028others(12): Show | 19 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1583-59C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134626 | ||||||
chr1:16134725
|
G | T | 11 | a0001c0036t0001g0115a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1583-158C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134725 | ||||||
chr1:16134799
|
C | T | 1 | a0001c0003t0001g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1583-232G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134799 | ||||||
chr1:16134841
|
C | T | 2 | a0001c0006t0001g0017a0001c0010t0001g0190 | 3 | HG00099.hp2 HG02300.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1582+195G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134841 | ||||||
chr1:16135338
|
C | T | 76 | a0001c0001t0001g0081a0001c0001t0001g0116a0001c0001t0001g0202others(73): Show | 84 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(81): Show |
intron_variant | MODIFIER | c.1429-149G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 6/16 | chr1 | 16135338 | ||||||
chr1:16135505
|
G | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0256a0001c0001t0001g0259others(2): Show | 5 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428+150C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 6/16 | chr1 | 16135505 | ||||||
chr1:16135645
|
T | G | 1 | a0001c0005t0001g0143 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1428+10A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 6/16 | chr1 | 16135645 | ||||||
chr1:16135790
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1313-20C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16135790 | ||||||
chr1:16135902
|
G | A | 1 | a0001c0003t0001g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1313-132C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16135902 | ||||||
chr1:16136150
|
C | T | 1 | a0001c0002t0002g0089 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1313-380G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136150 | ||||||
chr1:16136303
|
A | AAAT | 168 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1313-536_1313-534d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | ||||||
chr1:16136303
|
A | AAATAAT | 16 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0069others(13): Show | 16 | HG00438.hp1 HG01074.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.1313-539_1313-534d others(8): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | ||||||
chr1:16136303
|
A | AAATAATA others(2): Show |
19 | a0001c0002t0001g0076a0001c0002t0001g0254a0001c0004t0001g0260others(16): Show | 24 | HG00639.hp2 HG00738.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1313-542_1313-534d others(11): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | ||||||
chr1:16136303
|
A | AAATAATA others(5): Show |
13 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(10): Show | 14 | HG01069.hp1 HG01071.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1313-545_1313-534d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | ||||||
chr1:16136303
|
A | AAATAATA others(8): Show |
6 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0080others(3): Show | 7 | HG01106.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-548_1313-534d others(17): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | ||||||
chr1:16136303
|
A | AAATAATA others(11): Show |
1 | a0001c0005t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1313-551_1313-534d others(20): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | ||||||
chr1:16136303
|
AAATAATA others(5): Show |
A | 11 | a0001c0036t0001g0115a0002c0008t0003g0109a0002c0008t0003g0110others(8): Show | 11 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1313-545_1313-534d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | ||||||
chr1:16136384
|
C | T | 3 | a0001c0004t0001g0030a0001c0004t0001g0031a0001c0032t0001g0032 | 3 | HG00642.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1313-614G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136384 | ||||||
chr1:16136583
|
C | T | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1313-813G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136583 | ||||||
chr1:16136626
|
AAAG | A | 6 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(3): Show | 6 | HG01106.hp1 HG01167.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-859_1313-857d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136626 | ||||||
chr1:16136652
|
AAAGAAGA others(34): Show |
A | 5 | a0001c0001t0001g0116a0001c0003t0001g0205a0001c0003t0001g0207others(2): Show | 5 | HG00642.hp2 HG02451.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-923_1313-883d others(43): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136652 | ||||||
chr1:16136654
|
AGAAGAAG others(31): Show |
A | 7 | a0001c0003t0001g0208a0001c0003t0001g0209a0001c0003t0001g0224others(4): Show | 7 | HG01256.hp2 HG01934.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-922_1313-885d others(40): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136654 | ||||||
chr1:16136655
|
GAAGAAGA others(19): Show |
G | 23 | a0001c0003t0001g0027a0001c0003t0001g0167a0001c0003t0001g0195others(20): Show | 25 | HG00099.hp1 HG01884.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.1313-911_1313-886d others(28): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136655 | ||||||
chr1:16136657
|
AGAAGAAA others(28): Show |
A | 7 | a0001c0001t0001g0268a0001c0003t0001g0218a0001c0004t0001g0161others(4): Show | 7 | HG02300.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-922_1313-888d others(37): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136657 | ||||||
chr1:16136660
|
AGAAAAGA others(25): Show |
A | 8 | a0001c0003t0001g0210a0001c0003t0001g0212a0001c0003t0001g0215others(5): Show | 10 | HG01891.hp2 HG02135.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-922_1313-891d others(34): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136660 | ||||||
chr1:16136661
|
GAAAAGAA others(13): Show |
G | 4 | a0001c0003t0001g0214a0001c0003t0001g0219a0001c0004t0001g0028others(1): Show | 5 | HG01109.hp1 HG02622.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-911_1313-892d others(22): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136661 | ||||||
chr1:16136663
|
AAAGAAGA others(7): Show |
A | 1 | a0001c0003t0001g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1313-907_1313-894d others(16): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136663 | ||||||
chr1:16136664
|
A | G | 8 | a0001c0003t0001g0002a0001c0003t0001g0198a0001c0003t0001g0199others(5): Show | 10 | HG02738.hp1 HG02922.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.1313-894T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136664 | ||||||
chr1:16136666
|
GAAGAAAA others(10): Show |
G | 4 | a0001c0003t0001g0002a0001c0003t0001g0198a0001c0003t0001g0199others(1): Show | 6 | HG02738.hp1 HG03017.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-913_1313-897d others(19): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136666 | ||||||
chr1:16136666
|
GAAGAAAA others(39): Show |
G | 2 | a0001c0004t0002g0087a0001c0010t0001g0203 | 2 | HG02922.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1313-942_1313-897d others(48): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136666 | ||||||
chr1:16136666
|
GAAGAAAA others(42): Show |
G | 2 | a0001c0003t0001g0206a0001c0004t0001g0107 | 2 | NA18951.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1313-945_1313-897d others(51): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136666 | ||||||
chr1:16136678
|
A | G | 1 | a0001c0003t0001g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1313-908T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136678 | ||||||
chr1:16136681
|
A | G | 1 | a0001c0003t0001g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1313-911T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136681 | ||||||
chr1:16136686
|
A | G | 4 | a0001c0003t0001g0214a0001c0003t0001g0219a0001c0004t0001g0028others(1): Show | 5 | HG01109.hp1 HG02622.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-916T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136686 | ||||||
chr1:16136692
|
G | A | 9 | a0001c0003t0001g0002a0001c0003t0001g0198a0001c0003t0001g0199others(6): Show | 12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1313-922C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136692
|
GGAAGAAG others(16): Show |
G | 4 | a0001c0002t0001g0078a0006c0013t0003g0077a0006c0013t0003g0128others(1): Show | 4 | HG03130.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-945_1313-923d others(25): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136692
|
GGAAGAAG others(19): Show |
G | 7 | a0001c0001t0001g0259a0001c0002t0001g0080a0001c0002t0001g0265others(4): Show | 7 | HG02486.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-948_1313-923d others(28): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136692
|
GGAAGAAG others(22): Show |
G | 5 | a0001c0001t0001g0256a0001c0002t0001g0011a0001c0002t0001g0076others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-951_1313-923d others(31): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136692
|
GGAAGAAG others(25): Show |
G | 1 | a0002c0008t0003g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1313-954_1313-923d others(34): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136692
|
GGAAGAAG others(28): Show |
G | 1 | a0002c0035t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1313-957_1313-923d others(37): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136692
|
GGAAGAAG others(31): Show |
G | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1313-960_1313-923d others(40): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136692
|
GGAAGAAG others(34): Show |
G | 1 | a0001c0001t0001g0225 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1313-963_1313-923d others(43): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | ||||||
chr1:16136693
|
GAAGAAGA others(13): Show |
G | 4 | a0001c0001t0001g0081a0001c0002t0001g0034a0001c0002t0001g0232others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-943_1313-924d others(22): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136693 | ||||||
chr1:16136696
|
GAAGAAGA others(10): Show |
G | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1313-943_1313-927d others(19): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136696 | ||||||
chr1:16136698
|
A | G | 8 | a0001c0003t0001g0210a0001c0003t0001g0212a0001c0003t0001g0215others(5): Show | 10 | HG01891.hp2 HG02135.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-928T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136698 | ||||||
chr1:16136699
|
GAAGAAGA others(7): Show |
G | 3 | a0001c0001t0001g0099a0001c0002t0001g0254a0001c0036t0001g0115 | 3 | HG01167.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1313-943_1313-930d others(16): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136699 | ||||||
chr1:16136701
|
A | G | 7 | a0001c0001t0001g0268a0001c0003t0001g0218a0001c0004t0001g0161others(4): Show | 7 | HG02300.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-931T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136701 | ||||||
chr1:16136704
|
A | G | 8 | a0001c0003t0001g0208a0001c0003t0001g0209a0001c0003t0001g0224others(5): Show | 8 | HG00735.hp2 HG01256.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313-934T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136704 | ||||||
chr1:16136707
|
A | G | 5 | a0001c0001t0001g0116a0001c0003t0001g0205a0001c0003t0001g0207others(2): Show | 5 | HG00642.hp2 HG02451.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-937T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136707 | ||||||
chr1:16136708
|
GAAGAA | G | 12 | a0001c0003t0001g0027a0001c0003t0001g0195a0001c0003t0001g0200others(9): Show | 14 | HG00099.hp1 HG02027.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1313-943_1313-939d others(7): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136708 | ||||||
chr1:16136711
|
GAA | G | 45 | a0001c0001t0001g0116a0001c0001t0001g0268a0001c0003t0001g0002others(42): Show | 50 | HG00642.hp2 HG01109.hp1 HG01256.hp2 others(47): Show |
intron_variant | MODIFIER | c.1313-943_1313-942d others(4): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136711 | ||||||
chr1:16136713
|
A | AAAG | 24 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0038others(21): Show | 27 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1313-946_1313-944d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AAAGAAG | 17 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0040others(14): Show | 24 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1313-949_1313-944d others(8): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AAAGAAGA others(2): Show |
25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0020others(22): Show | 32 | HG00323.hp2 HG00597.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1313-952_1313-944d others(11): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AAAGAAGA others(5): Show |
17 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0058others(14): Show | 19 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.1313-955_1313-944d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AAAGAAGA others(8): Show |
12 | a0001c0001t0001g0049a0001c0001t0001g0101a0001c0001t0001g0165others(9): Show | 14 | HG01109.hp2 HG01123.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1313-958_1313-944d others(17): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AAAGAAGA others(11): Show |
5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0272others(2): Show | 6 | HG00280.hp2 HG01261.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1313-961_1313-944d others(20): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AAAGAAGA others(14): Show |
4 | a0001c0001t0001g0182a0001c0001t0001g0239a0001c0005t0001g0004others(1): Show | 6 | HG00639.hp1 HG01516.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1313-964_1313-944d others(23): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AAAGAAGA others(23): Show |
1 | a0013c0029t0001g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1313-973_1313-944d others(32): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AG | 6 | a0001c0001t0001g0035a0001c0001t0002g0045a0001c0003t0001g0197others(3): Show | 6 | HG01884.hp2 HG02056.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-944_1313-943i others(3): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AGAAGAAG others(3): Show |
2 | a0001c0001t0002g0188a0001c0005t0007g0127 | 2 | HG02559.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1313-944_1313-943i others(12): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AGAAGAAG others(6): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0169 | 2 | HG00280.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1313-944_1313-943i others(15): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AGAAGAAG others(9): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0056a0001c0001t0001g0181 | 3 | HG00558.hp2 NA18954.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1313-944_1313-943i others(18): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | AGAAGAAG others(18): Show |
1 | a0001c0001t0001g0070 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1313-944_1313-943i others(27): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
A | G | 2 | a0001c0004t0002g0087a0001c0010t0001g0203 | 2 | HG02922.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1313-943T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
AAAG | A | 25 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0096others(22): Show | 27 | HG00609.hp1 HG00733.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1313-946_1313-944d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
AAAGAAG | A | 8 | a0001c0001t0001g0173a0001c0001t0002g0024a0001c0001t0002g0100others(5): Show | 10 | HG00099.hp2 HG01069.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1313-949_1313-944d others(8): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
AAAGAAGA others(5): Show |
A | 1 | a0001c0006t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1313-955_1313-944d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136713
|
AAAGAAGA others(8): Show |
A | 1 | a0001c0001t0001g0044 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1313-958_1313-944d others(17): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | ||||||
chr1:16136757
|
A | G | 1 | a0001c0004t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1313-987T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136757 | ||||||
chr1:16136763
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1313-993T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136763 | ||||||
chr1:16136773
|
G | C | 4 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(1): Show | 4 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-1003C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136773 | ||||||
chr1:16136773
|
G | GAAGAAGA others(5): Show |
1 | a0001c0002t0001g0178 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1313-1004_1313-100 others(16): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136773 | ||||||
chr1:16136797
|
CT | C | 23 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(20): Show | 24 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.1313-1028delA | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136797 | ||||||
chr1:16136861
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1312+992G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136861 | ||||||
chr1:16136934
|
G | A | 1 | a0001c0006t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1312+919C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136934 | ||||||
chr1:16136978
|
T | G | 1 | a0005c0017t0001g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1312+875A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136978 | ||||||
chr1:16137148
|
A | T | 63 | a0001c0001t0001g0116a0001c0001t0001g0268a0001c0003t0001g0002others(60): Show | 70 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.1312+705T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137148 | ||||||
chr1:16137191
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1312+662C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137191 | ||||||
chr1:16137297
|
T | TAA | 28 | a0001c0001t0001g0081a0001c0001t0001g0202a0001c0001t0001g0225others(25): Show | 29 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1312+554_1312+555d others(4): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137297 | ||||||
chr1:16137297
|
T | TAAA | 58 | a0001c0001t0001g0116a0001c0001t0001g0268a0001c0003t0001g0002others(55): Show | 65 | HG00099.hp1 HG01109.hp1 HG01256.hp2 others(62): Show |
intron_variant | MODIFIER | c.1312+553_1312+555d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137297 | ||||||
chr1:16137337
|
G | T | 10 | a0001c0001t0001g0268a0001c0003t0001g0204a0001c0003t0001g0219others(7): Show | 10 | HG00642.hp2 HG01109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312+516C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137337 | ||||||
chr1:16137394
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1312+459G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137394 | ||||||
chr1:16137553
|
A | G | 28 | a0001c0004t0001g0006a0001c0004t0001g0028a0001c0004t0001g0258others(25): Show | 31 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1312+300T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137553 | ||||||
chr1:16137645
|
A | G | 4 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(1): Show | 4 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312+208T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137645 | ||||||
chr1:16137765
|
T | C | 53 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0268others(50): Show | 57 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1312+88A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137765 | ||||||
chr1:16138441
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0225a0001c0003t0001g0204others(2): Show | 5 | HG01109.hp1 HG02683.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-11G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138441 | ||||||
chr1:16138802
|
C | T | 13 | a0001c0001t0001g0099a0001c0001t0001g0256a0001c0001t0001g0259others(10): Show | 13 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-372G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138802 | ||||||
chr1:16138908
|
A | G | 64 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(61): Show | 71 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.824-478T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138908 | ||||||
chr1:16138909
|
C | T | 64 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0041others(61): Show | 71 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.824-479G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138909 | ||||||
chr1:16139001
|
C | T | 10 | a0001c0001t0001g0081a0001c0002t0001g0011a0001c0002t0001g0034others(7): Show | 11 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-571G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139001 | ||||||
chr1:16139306
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.824-876G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139306 | ||||||
chr1:16139508
|
T | C | 58 | a0001c0001t0001g0116a0001c0001t0001g0202a0001c0001t0001g0225others(55): Show | 64 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.824-1078A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139508 | ||||||
chr1:16139699
|
G | A | 3 | a0004c0011t0001g0262a0004c0011t0001g0263a0004c0011t0001g0264 | 3 | HG02257.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.824-1269C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139699 | ||||||
chr1:16139752
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0072a0001c0001t0002g0188others(1): Show | 5 | NA18961.hp1 NA18985.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-1322C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139752 | ||||||
chr1:16139795
|
G | A | 1 | a0001c0024t0003g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.824-1365C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139795 | ||||||
chr1:16139947
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.824-1517G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139947 | ||||||
chr1:16140039
|
G | A | 6 | a0001c0001t0001g0268a0001c0003t0001g0197a0001c0003t0001g0212others(3): Show | 6 | HG02027.hp2 HG02572.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1609C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140039 | ||||||
chr1:16140085
|
G | A | 1 | a0001c0003t0001g0218 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.824-1655C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140085 | ||||||
chr1:16140087
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.824-1657C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140087 | ||||||
chr1:16140176
|
G | A | 1 | a0011c0022t0001g0274 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.824-1746C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140176 | ||||||
chr1:16140204
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.824-1774G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140204 | ||||||
chr1:16140232
|
G | A | 1 | a0001c0033t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.824-1802C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140232 | ||||||
chr1:16140397
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.824-1967G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140397 | ||||||
chr1:16140767
|
G | A | 1 | a0001c0003t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-2337C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140767 | ||||||
chr1:16140771
|
A | G | 4 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0004t0001g0258others(1): Show | 4 | HG01106.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-2341T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140771 | ||||||
chr1:16140853
|
G | A | 23 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0256others(20): Show | 24 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.824-2423C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140853 | ||||||
chr1:16140890
|
C | T | 1 | a0001c0009t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.824-2460G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140890 | ||||||
chr1:16140896
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.824-2466G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140896 | ||||||
chr1:16141150
|
T | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(153): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.824-2720A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141150 | ||||||
chr1:16141429
|
G | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.824-2999C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141429 | ||||||
chr1:16141478
|
G | A | 22 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0256others(19): Show | 23 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-3048C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141478 | ||||||
chr1:16141680
|
C | T | 9 | a0001c0001t0001g0116a0001c0004t0002g0087a0001c0004t0002g0108others(6): Show | 9 | HG02451.hp1 HG02572.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-3250G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141680 | ||||||
chr1:16141710
|
C | T | 1 | a0001c0004t0001g0201 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824-3280G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141710 | ||||||
chr1:16141730
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.824-3300T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141730 | ||||||
chr1:16142040
|
C | T | 1 | a0001c0027t0001g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824-3610G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142040 | ||||||
chr1:16142372
|
T | A | 22 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0256others(19): Show | 23 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-3942A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142372 | ||||||
chr1:16142463
|
A | G | 2 | a0001c0001t0002g0100a0001c0001t0002g0230 | 2 | NA18975.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.824-4033T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142463 | ||||||
chr1:16142627
|
ATGGATGG others(129): Show |
A | 1 | a0001c0001t0001g0056 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.824-4333_824-4198d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142627 | ||||||
chr1:16142684
|
G | A | 14 | a0001c0001t0001g0099a0001c0001t0001g0256a0001c0001t0001g0259others(11): Show | 14 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.824-4254C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142684 | ||||||
chr1:16142789
|
A | G | 22 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0256others(19): Show | 23 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-4359T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142789 | ||||||
chr1:16142814
|
CGGGATGG others(124): Show |
C | 1 | a0001c0015t0001g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.824-4515_824-4385d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142814 | ||||||
chr1:16142869
|
G | A | 4 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0004t0001g0258others(1): Show | 4 | HG01106.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-4439C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142869 | ||||||
chr1:16142984
|
A | AATGG | 11 | a0001c0001t0001g0099a0001c0001t0001g0259a0001c0002t0001g0254others(8): Show | 11 | HG00673.hp1 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-4558_824-4555d others(6): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | ||||||
chr1:16142984
|
A | AATGGATG others(1): Show |
130 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.824-4562_824-4555d others(10): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | ||||||
chr1:16142984
|
A | AATGGATG others(5): Show |
20 | a0001c0001t0001g0038a0001c0001t0001g0174a0001c0001t0001g0175others(17): Show | 20 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.824-4566_824-4555d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | ||||||
chr1:16142984
|
A | AATGGATG others(9): Show |
1 | a0001c0036t0001g0115 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.824-4570_824-4555d others(18): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | ||||||
chr1:16143134
|
C | T | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.824-4704G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143134 | ||||||
chr1:16143158
|
T | TGATG | 93 | a0001c0001t0001g0101a0001c0001t0001g0162a0001c0001t0001g0170others(90): Show | 106 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.824-4732_824-4729d others(6): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | ||||||
chr1:16143158
|
T | TGATGGAT others(1): Show |
142 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(139): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.824-4736_824-4729d others(10): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | ||||||
chr1:16143158
|
T | TGATGGAT others(5): Show |
22 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0099others(19): Show | 22 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.824-4740_824-4729d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | ||||||
chr1:16143158
|
T | TGATGGAT others(9): Show |
6 | a0001c0002t0001g0011a0001c0002t0001g0034a0001c0002t0001g0078others(3): Show | 7 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-4744_824-4729d others(18): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | ||||||
chr1:16143191
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 5 | HG00280.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-4761T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143191 | ||||||
chr1:16143251
|
G | C | 1 | a0002c0035t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.824-4821C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143251 | ||||||
chr1:16143322
|
T | C | 1 | a0001c0003t0001g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.824-4892A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143322 | ||||||
chr1:16143430
|
C | T | 20 | a0001c0001t0001g0081a0001c0001t0001g0099a0001c0001t0001g0256others(17): Show | 21 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.823+4948G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143430 | ||||||
chr1:16143436
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.823+4942A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143436 | ||||||
chr1:16143442
|
AC | A | 8 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+4935delG | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143442 | ||||||
chr1:16143533
|
A | G | 2 | a0001c0006t0001g0083a0001c0006t0001g0126 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.823+4845T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143533 | ||||||
chr1:16143921
|
G | A | 8 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+4457C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143921 | ||||||
chr1:16143937
|
C | G | 1 | a0001c0003t0001g0197 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.823+4441G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143937 | ||||||
chr1:16144047
|
C | T | 1 | a0001c0004t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823+4331G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144047 | ||||||
chr1:16144191
|
C | T | 8 | a0001c0001t0001g0081a0001c0002t0001g0011a0001c0002t0001g0034others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+4187G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144191 | ||||||
chr1:16144295
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.823+4083C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144295 | ||||||
chr1:16144383
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 5 | HG02129.hp2 NA18944.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+3995C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144383 | ||||||
chr1:16144447
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.823+3931G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144447 | ||||||
chr1:16144505
|
G | T | 69 | a0001c0001t0001g0099a0001c0002t0001g0196a0001c0005t0001g0004others(66): Show | 81 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.823+3873C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144505 | ||||||
chr1:16144648
|
C | T | 1 | a0001c0016t0001g0013 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.823+3730G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144648 | ||||||
chr1:16144673
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823+3705A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144673 | ||||||
chr1:16144791
|
T | A | 1 | a0001c0027t0001g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823+3587A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144791 | ||||||
chr1:16144798
|
CCCCCGTT | C | 18 | a0001c0001t0001g0081a0001c0001t0001g0256a0001c0001t0001g0259others(15): Show | 19 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.823+3573_823+3579d others(9): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144798 | ||||||
chr1:16144960
|
A | G | 71 | a0001c0001t0001g0099a0001c0002t0001g0034a0001c0002t0001g0078others(68): Show | 83 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.823+3418T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144960 | ||||||
chr1:16145202
|
G | A | 2 | a0002c0008t0003g0117a0002c0008t0003g0118 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+3176C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145202 | ||||||
chr1:16145202
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0058others(3): Show | 7 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+3176C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145202 | ||||||
chr1:16145247
|
G | T | 1 | a0010c0025t0001g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.823+3131C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145247 | ||||||
chr1:16145289
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.823+3089C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145289 | ||||||
chr1:16145333
|
G | A | 2 | a0001c0001t0001g0081a0001c0004t0001g0194 | 2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.823+3045C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145333 | ||||||
chr1:16145341
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.823+3037G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145341 | ||||||
chr1:16145454
|
C | G | 1 | a0002c0008t0003g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.823+2924G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145454 | ||||||
chr1:16145511
|
C | T | 8 | a0001c0001t0001g0081a0001c0002t0001g0011a0001c0002t0001g0034others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+2867G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145511 | ||||||
chr1:16145535
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.823+2843C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145535 | ||||||
chr1:16145791
|
C | T | 1 | a0003c0007t0001g0124 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.823+2587G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145791 | ||||||
chr1:16145840
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.823+2538A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145840 | ||||||
chr1:16145881
|
T | C | 1 | a0013c0029t0001g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.823+2497A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145881 | ||||||
chr1:16145940
|
C | G | 1 | a0001c0003t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.823+2438G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145940 | ||||||
chr1:16146015
|
A | G | 16 | a0001c0001t0001g0081a0001c0001t0001g0256a0001c0001t0001g0259others(13): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2363T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146015 | ||||||
chr1:16146037
|
G | A | 1 | a0006c0013t0003g0077 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823+2341C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146037 | ||||||
chr1:16146111
|
C | T | 16 | a0001c0001t0001g0081a0001c0001t0001g0256a0001c0001t0001g0259others(13): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2267G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146111 | ||||||
chr1:16146125
|
C | A | 16 | a0001c0001t0001g0081a0001c0001t0001g0256a0001c0001t0001g0259others(13): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2253G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146125 | ||||||
chr1:16146184
|
C | T | 2 | a0002c0008t0003g0117a0002c0008t0003g0118 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+2194G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146184 | ||||||
chr1:16146223
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0003t0001g0167 | 3 | HG01074.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.823+2155G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146223 | ||||||
chr1:16146234
|
G | C | 16 | a0001c0001t0001g0081a0001c0001t0001g0256a0001c0001t0001g0259others(13): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2144C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146234 | ||||||
chr1:16146293
|
G | T | 1 | a0001c0001t0002g0036 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.823+2085C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146293 | ||||||
chr1:16146329
|
G | T | 2 | a0002c0008t0003g0117a0002c0008t0003g0118 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+2049C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146329 | ||||||
chr1:16146339
|
C | A | 36 | a0001c0001t0001g0202a0001c0001t0001g0225a0001c0001t0001g0268others(33): Show | 37 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.823+2039G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146339 | ||||||
chr1:16146391
|
C | T | 1 | a0002c0035t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823+1987G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146391 | ||||||
chr1:16146408
|
C | T | 1 | a0001c0004t0002g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+1970G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146408 | ||||||
chr1:16146432
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.823+1946C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146432 | ||||||
chr1:16146464
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.823+1914G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146464 | ||||||
chr1:16146498
|
C | T | 68 | a0001c0005t0001g0004a0001c0005t0001g0014a0001c0005t0001g0015others(65): Show | 80 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.823+1880G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146498 | ||||||
chr1:16146591
|
G | A | 1 | a0001c0006t0001g0123 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.823+1787C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146591 | ||||||
chr1:16146592
|
G | A | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.823+1786C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146592 | ||||||
chr1:16146595
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.823+1783G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146595 | ||||||
chr1:16146599
|
T | G | 1 | a0005c0017t0001g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.823+1779A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146599 | ||||||
chr1:16146621
|
C | G | 1 | a0001c0002t0004g0093 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.823+1757G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146621 | ||||||
chr1:16146642
|
A | G | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.823+1736T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146642 | ||||||
chr1:16146718
|
C | T | 2 | a0001c0006t0001g0123a0009c0028t0001g0122 | 2 | HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.823+1660G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146718 | ||||||
chr1:16146801
|
G | T | 1 | a0002c0035t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823+1577C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146801 | ||||||
chr1:16146888
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.823+1490A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146888 | ||||||
chr1:16147019
|
A | G | 80 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(77): Show | 92 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.823+1359T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147019 | ||||||
chr1:16147096
|
A | G | 1 | a0001c0004t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+1282T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147096 | ||||||
chr1:16147163
|
C | T | 1 | a0001c0024t0003g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+1215G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147163 | ||||||
chr1:16147266
|
G | T | 1 | a0001c0004t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+1112C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147266 | ||||||
chr1:16147275
|
T | C | 11 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(8): Show | 11 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.823+1103A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147275 | ||||||
chr1:16147450
|
G | A | 7 | a0001c0001t0001g0081a0001c0002t0001g0011a0001c0002t0001g0034others(4): Show | 8 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+928C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147450 | ||||||
chr1:16147484
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(248): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.823+894A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147484 | ||||||
chr1:16147546
|
G | A | 8 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+832C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147546 | ||||||
chr1:16147561
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.823+817G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147561 | ||||||
chr1:16147615
|
C | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.823+763G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147615 | ||||||
chr1:16147631
|
C | T | 9 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(6): Show | 9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+747G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147631 | ||||||
chr1:16147633
|
T | C | 2 | a0002c0008t0003g0117a0002c0008t0003g0118 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+745A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147633 | ||||||
chr1:16147772
|
C | T | 1 | a0001c0004t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+606G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147772 | ||||||
chr1:16147865
|
T | G | 9 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(6): Show | 9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+513A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147865 | ||||||
chr1:16147922
|
A | G | 9 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(6): Show | 9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+456T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147922 | ||||||
chr1:16148059
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.823+319T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148059 | ||||||
chr1:16148068
|
G | A | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.823+310C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148068 | ||||||
chr1:16148169
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.823+209G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148169 | ||||||
chr1:16148206
|
G | A | 105 | a0001c0001t0001g0081a0001c0001t0001g0101a0001c0001t0001g0256others(102): Show | 118 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.823+172C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148206 | ||||||
chr1:16148344
|
AC | A | 105 | a0001c0001t0001g0081a0001c0001t0001g0101a0001c0001t0001g0256others(102): Show | 118 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.823+33delG | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148344 | ||||||
chr1:16149161
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02071.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.154-114C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149161 | ||||||
chr1:16149185
|
C | T | 2 | a0001c0004t0001g0233a0001c0004t0001g0250 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154-138G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149185 | ||||||
chr1:16149247
|
T | C | 1 | a0001c0005t0001g0158 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154-200A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149247 | ||||||
chr1:16149252
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-205C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149252 | ||||||
chr1:16149318
|
G | C | 9 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0254others(6): Show | 9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-271C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149318 | ||||||
chr1:16149385
|
G | T | 1 | a0001c0004t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.154-338C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149385 | ||||||
chr1:16149460
|
G | A | 1 | a0001c0004t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.154-413C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149460 | ||||||
chr1:16149509
|
C | T | 1 | a0002c0035t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-462G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149509 | ||||||
chr1:16149517
|
T | C | 1 | a0001c0027t0001g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.154-470A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149517 | ||||||
chr1:16149563
|
T | G | 1 | a0001c0026t0001g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154-516A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149563 | ||||||
chr1:16149601
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.154-554T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149601 | ||||||
chr1:16149748
|
C | T | 4 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0091others(1): Show | 4 | HG00733.hp2 HG01074.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-701G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149748 | ||||||
chr1:16149913
|
A | G | 1 | a0001c0006t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154-866T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149913 | ||||||
chr1:16149938
|
A | G | 2 | a0002c0008t0003g0117a0002c0008t0003g0118 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-891T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149938 | ||||||
chr1:16149965
|
G | A | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154-918C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149965 | ||||||
chr1:16150002
|
C | T | 9 | a0001c0001t0001g0116a0001c0004t0002g0087a0001c0004t0002g0108others(6): Show | 9 | HG02451.hp1 HG02572.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+894G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150002 | ||||||
chr1:16150125
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.153+771G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150125 | ||||||
chr1:16150186
|
C | T | 1 | a0001c0004t0001g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.153+710G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150186 | ||||||
chr1:16150271
|
G | A | 8 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0034others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+625C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150271 | ||||||
chr1:16150329
|
C | T | 9 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0034others(6): Show | 9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+567G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150329 | ||||||
chr1:16150768
|
G | A | 2 | a0002c0008t0003g0117a0002c0008t0003g0118 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.153+128C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150768 | ||||||
chr1:16150810
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.153+86G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150810 | ||||||
chr1:16151515
|
GGTA | G | 10 | a0001c0002t0001g0265a0001c0004t0001g0006a0001c0004t0001g0028others(7): Show | 13 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.86-555_86-553delTA others(1): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151515 | ||||||
chr1:16151578
|
G | A | 1 | a0001c0005t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.86-615C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151578 | ||||||
chr1:16151594
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.86-631A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151594 | ||||||
chr1:16151621
|
G | T | 1 | a0006c0013t0003g0077 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.86-658C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151621 | ||||||
chr1:16151835
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.86-872A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151835 | ||||||
chr1:16151837
|
C | T | 1 | a0011c0022t0001g0274 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.86-874G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151837 | ||||||
chr1:16151949
|
A | C | 1 | a0001c0006t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.86-986T>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151949 | ||||||
chr1:16151966
|
A | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.86-1003T>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151966 | ||||||
chr1:16152022
|
A | G | 7 | a0001c0004t0001g0006a0001c0004t0001g0161a0001c0004t0001g0261others(4): Show | 9 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-1059T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152022 | ||||||
chr1:16152072
|
C | T | 10 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0034others(7): Show | 10 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.86-1109G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152072 | ||||||
chr1:16152159
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(145): Show | 173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.86-1196G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152159 | ||||||
chr1:16152438
|
G | C | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.86-1475C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152438 | ||||||
chr1:16152686
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.86-1723A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152686 | ||||||
chr1:16152822
|
G | A | 1 | a0001c0004t0001g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.86-1859C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152822 | ||||||
chr1:16152905
|
C | T | 1 | a0001c0004t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-1942G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152905 | ||||||
chr1:16152951
|
G | A | 1 | a0001c0003t0001g0224 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.86-1988C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152951 | ||||||
chr1:16153010
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-2047A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153010 | ||||||
chr1:16153041
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.86-2078C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153041 | ||||||
chr1:16153130
|
GA | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.86-2168delT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153130 | ||||||
chr1:16153131
|
A | G | 1 | a0001c0004t0002g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.86-2168T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153131 | ||||||
chr1:16153257
|
G | C | 8 | a0001c0001t0001g0081a0001c0002t0001g0011a0001c0002t0001g0076others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-2294C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153257 | ||||||
chr1:16153435
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.85+2413G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153435 | ||||||
chr1:16153687
|
G | C | 1 | a0002c0035t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.85+2161C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153687 | ||||||
chr1:16153928
|
T | C | 1 | a0001c0002t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.85+1920A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153928 | ||||||
chr1:16153977
|
C | G | 1 | a0001c0002t0001g0254 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.85+1871G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153977 | ||||||
chr1:16153977
|
C | T | 8 | a0001c0001t0001g0081a0001c0002t0001g0011a0001c0002t0001g0076others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+1871G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153977 | ||||||
chr1:16154293
|
T | C | 2 | a0002c0035t0003g0252a0013c0029t0001g0119 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.85+1555A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154293 | ||||||
chr1:16154374
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0010t0001g0066 | 4 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+1474C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154374 | ||||||
chr1:16154502
|
G | C | 22 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0268others(19): Show | 25 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.85+1346C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154502 | ||||||
chr1:16154513
|
G | T | 1 | a0001c0002t0001g0076 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.85+1335C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154513 | ||||||
chr1:16154656
|
T | C | 1 | a0001c0004t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+1192A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154656 | ||||||
chr1:16154756
|
C | CA | 173 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(170): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.85+1091dupT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | ||||||
chr1:16154756
|
C | CAA | 28 | a0001c0001t0001g0010a0001c0001t0001g0067a0001c0001t0001g0068others(25): Show | 29 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.85+1090_85+1091dup others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | ||||||
chr1:16154756
|
CA | C | 19 | a0001c0001t0001g0081a0001c0001t0001g0268a0001c0002t0001g0011others(16): Show | 23 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+1091delT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | ||||||
chr1:16154756
|
CAA | C | 8 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0002t0001g0034others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+1090_85+1091del others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | ||||||
chr1:16154756
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0075a0001c0003t0001g0002 | 4 | HG02738.hp1 HG03704.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+1081_85+1091del others(11): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | ||||||
chr1:16154847
|
G | A | 1 | a0001c0015t0001g0253 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.85+1001C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154847 | ||||||
chr1:16154871
|
C | T | 45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(42): Show | 49 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.85+977G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154871 | ||||||
chr1:16154991
|
G | A | 22 | a0001c0001t0001g0256a0001c0001t0001g0259a0001c0001t0001g0268others(19): Show | 25 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.85+857C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154991 | ||||||
chr1:16155249
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85+599C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155249 | ||||||
chr1:16155395
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.85+453G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155395 | ||||||
chr1:16155497
|
C | A | 1 | a0001c0034t0001g0273 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.85+351G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155497 | ||||||
chr1:16155670
|
A | G | 1 | a0001c0002t0002g0033 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.85+178T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155670 | ||||||
chr1:16155675
|
C | G | 3 | a0001c0004t0001g0030a0001c0004t0001g0031a0001c0032t0001g0032 | 3 | HG00642.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.85+173G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155675 | ||||||
chr1:16155769
|
T | C | 1 | a0011c0022t0001g0274 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+79A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155769 |