Item | Value |
---|---|
geneid | 2053 |
ensemblid | ENSG00000120915.14 |
hgncid | 3402 |
symbol | EPHX2 |
name | epoxide hydrolase 2 |
refseq_nuc | NM_001979.6 |
refseq_prot | NP_001970.2 |
ensembl_nuc | ENST00000521400.6 |
ensembl_prot | ENSP00000430269.1 |
mane_status | MANE Select |
chr | chr8 |
start | 27491143 |
end | 27545564 |
strand | + |
ver | v1.2 |
region | chr8:27491143-27545564 |
region5000 | chr8:27486143-27550564 |
regionname0 | EPHX2_chr8_27491143_27545564 |
regionname5000 | EPHX2_chr8_27486143_27550564 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 555 | 244 | 56 | 36 | 117 | 6 | 27 | 87 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0002 | 0/0 | 555 | 62 | 5 | 5 | 43 | 3 | 6 | 38 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0003 | 0/0 | 555 | 26 | 17 | 5 | 0 | 0 | 4 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0004 | 0/0 | 555 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0005 | 0/0 | 555 | 7 | 0 | 0 | 7 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0006 | 0/0 | 555 | 5 | 1 | 3 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0007 | 0/0 | 556 | 4 | 0 | 2 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0008 | 0/0 | 555 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0009 | 0/0 | 556 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0010 | 0/0 | 555 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0011 | 0/0 | 555 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0012 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0013 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0014 | 0/0 | 555 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0015 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0016 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0017 | 0/0 | 555 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0018 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0019 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0020 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1668 | 137 | 14 | 32 | 66 | 4 | 19 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0002 | 0/0 | 1668 | 59 | 8 | 2 | 40 | 2 | 7 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0003 | 0/0 | 1668 | 49 | 5 | 4 | 33 | 1 | 6 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0004 | 0/0 | 1668 | 21 | 21 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0005 | 0/0 | 1668 | 16 | 10 | 0 | 6 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0006 | 0/0 | 1668 | 13 | 5 | 4 | 0 | 0 | 4 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0007 | 0/0 | 1668 | 12 | 11 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0008 | 0/0 | 1668 | 9 | 0 | 1 | 8 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0009 | 0/0 | 1668 | 7 | 0 | 0 | 7 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0010 | 0/0 | 1668 | 7 | 5 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0011 | 0/0 | 1668 | 4 | 0 | 0 | 2 | 2 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0012 | 0/0 | 1671 | 3 | 0 | 2 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0013 | 0/0 | 1668 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0014 | 0/0 | 1668 | 3 | 2 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0015 | 0/0 | 1668 | 3 | 3 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0016 | 0/0 | 1668 | 3 | 0 | 3 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0017 | 0/0 | 1668 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0018 | 0/0 | 1671 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0019 | 0/0 | 1668 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0020 | 0/0 | 1668 | 2 | 1 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0021 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0022 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0023 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0024 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0025 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0026 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0027 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0028 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0029 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0030 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0031 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0032 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0033 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0034 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0035 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0036 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
c0037 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1109 | 170 | 21 | 41 | 77 | 9 | 20 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0002 | 0/0 | 1109 | 96 | 21 | 7 | 55 | 2 | 11 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0003 | 0/0 | 1109 | 71 | 25 | 5 | 34 | 1 | 6 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0004 | 0/0 | 1109 | 22 | 20 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0005 | 0/0 | 1109 | 4 | 0 | 0 | 4 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0006 | 0/0 | 1109 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0007 | 0/0 | 1109 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0008 | 0/0 | 1109 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0009 | 0/0 | 1109 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0010 | 0/0 | 1109 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0011 | 0/0 | 1109 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
t0012 | 0/0 | 1109 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1668 | 137 | 14 | 32 | 66 | 4 | 19 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0002 | 0/0 | 1668 | 59 | 8 | 2 | 40 | 2 | 7 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0004 | 0/0 | 1668 | 21 | 21 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0005 | 0/0 | 1668 | 16 | 10 | 0 | 6 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0013 | 0/0 | 1668 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0014 | 0/0 | 1668 | 3 | 2 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0017 | 0/0 | 1668 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0025 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0031 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0001c0032 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0002c0003 | 0/0 | 1668 | 49 | 5 | 4 | 33 | 1 | 6 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0002c0008 | 0/0 | 1668 | 9 | 0 | 1 | 8 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0002c0011 | 0/0 | 1668 | 4 | 0 | 0 | 2 | 2 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0003c0006 | 0/0 | 1668 | 13 | 5 | 4 | 0 | 0 | 4 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0003c0007 | 0/0 | 1668 | 12 | 11 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0003c0035 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0004c0010 | 0/0 | 1668 | 7 | 5 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0004c0015 | 0/0 | 1668 | 3 | 3 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0005c0009 | 0/0 | 1668 | 7 | 0 | 0 | 7 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0006c0016 | 0/0 | 1668 | 3 | 0 | 3 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0006c0020 | 0/0 | 1668 | 2 | 1 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0007c0012 | 0/0 | 1671 | 3 | 0 | 2 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0007c0029 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0008c0019 | 0/0 | 1668 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0008c0034 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0009c0018 | 0/0 | 1671 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0010c0021 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0011c0033 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0012c0023 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0013c0028 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0014c0027 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0015c0024 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0016c0026 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0017c0030 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0018c0022 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0019c0037 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 | |
a0020c0036 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2776 | 133 | 14 | 31 | 64 | 4 | 18 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0001t0006 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0001t0009 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0001t0010 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0001t0011 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0002t0002 | 0/0 | 2776 | 59 | 8 | 2 | 40 | 2 | 7 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0004t0003 | 0/0 | 2776 | 12 | 12 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0004t0004 | 0/0 | 2776 | 9 | 9 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0005t0002 | 0/0 | 2776 | 6 | 6 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0005t0003 | 0/0 | 2776 | 8 | 4 | 0 | 4 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0005t0005 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0005t0006 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0013t0002 | 0/0 | 2776 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0013t0006 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0014t0003 | 0/0 | 2776 | 3 | 2 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0017t0001 | 0/0 | 2776 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0025t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0031t0001 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0001c0032t0003 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0002c0003t0002 | 0/0 | 2776 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0002c0003t0003 | 0/0 | 2776 | 44 | 5 | 4 | 28 | 1 | 6 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0002c0003t0005 | 0/0 | 2776 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0002c0008t0002 | 0/0 | 2776 | 9 | 0 | 1 | 8 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0002c0011t0001 | 0/0 | 2776 | 4 | 0 | 0 | 2 | 2 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0003c0006t0002 | 0/0 | 2776 | 13 | 5 | 4 | 0 | 0 | 4 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0003c0007t0004 | 0/0 | 2776 | 9 | 8 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0003c0007t0008 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0003c0007t0012 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0003c0035t0001 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0004c0010t0001 | 0/0 | 2776 | 5 | 3 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0004c0010t0007 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0004c0015t0002 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0004c0015t0004 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0005c0009t0001 | 0/0 | 2776 | 7 | 0 | 0 | 7 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0006c0016t0001 | 0/0 | 2776 | 3 | 0 | 3 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0006c0020t0001 | 0/0 | 2776 | 2 | 1 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0007c0012t0001 | 0/0 | 2779 | 3 | 0 | 2 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0007c0029t0003 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0008c0019t0001 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0008c0034t0003 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0009c0018t0001 | 0/0 | 2779 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0010c0021t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0011c0033t0004 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0012c0023t0003 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0013c0028t0001 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0014c0027t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0015c0024t0002 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0016c0026t0002 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0017c0030t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0018c0022t0002 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0019c0037t0004 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
a0020c0036t0002 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | copy fasta | chr8 | 27486143 | 27550564 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0001t0011g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0004t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0005t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0013t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0013t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0013t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0014t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0014t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0014t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0017t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0017t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0025t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0031t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0001c0032t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0003t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0008t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0011t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0011t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0011t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0002c0011t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0006t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0007t0012g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0003c0035t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0010t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0010t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0010t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0010t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0010t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0010t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0010t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0015t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0015t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0004c0015t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0005c0009t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0005c0009t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0005c0009t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0005c0009t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0005c0009t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0005c0009t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0005c0009t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0006c0016t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0006c0016t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0006c0020t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0006c0020t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0007c0012t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0007c0012t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0007c0012t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0007c0029t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0008c0019t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0008c0019t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0008c0034t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0009c0018t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0009c0018t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0010c0021t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0011c0033t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0012c0023t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0013c0028t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0014c0027t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0015c0024t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0016c0026t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0017c0030t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0018c0022t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0019c0037t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
a0020c0036t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0003 | t0003 | g0023 | EUR | GBR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00323 | hp1 | a0006 | c0020 | t0001 | g0190 | EUR | FIN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00408 | hp2 | a0001 | c0005 | t0003 | g0168 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00544 | hp1 | a0002 | c0003 | t0003 | g0063 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00558 | hp2 | a0002 | c0003 | t0003 | g0003 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00597 | hp2 | a0005 | c0009 | t0001 | g0074 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00621 | hp2 | a0005 | c0009 | t0001 | g0071 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00639 | hp1 | a0009 | c0018 | t0001 | g0303 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00639 | hp2 | a0004 | c0010 | t0001 | g0298 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00642 | hp1 | a0003 | c0006 | t0002 | g0354 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00673 | hp2 | a0002 | c0003 | t0003 | g0003 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00733 | hp1 | a0003 | c0007 | t0004 | g0312 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00733 | hp2 | a0001 | c0031 | t0001 | g0191 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00738 | hp2 | a0011 | c0033 | t0004 | g0015 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01070 | hp1 | a0007 | c0012 | t0001 | g0301 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01106 | hp1 | a0003 | c0006 | t0002 | g0359 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01109 | hp1 | a0009 | c0018 | t0001 | g0300 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01167 | hp1 | a0003 | c0006 | t0002 | g0356 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01192 | hp1 | a0002 | c0003 | t0003 | g0032 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01192 | hp2 | a0004 | c0010 | t0001 | g0296 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01243 | hp2 | a0001 | c0014 | t0003 | g0346 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01257 | hp1 | a0006 | c0016 | t0001 | g0009 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01258 | hp1 | a0006 | c0016 | t0001 | g0009 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01261 | hp2 | a0002 | c0003 | t0003 | g0216 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01361 | hp1 | a0006 | c0016 | t0001 | g0184 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0270 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01515 | hp2 | a0014 | c0027 | t0001 | g0161 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01516 | hp1 | a0002 | c0011 | t0001 | g0222 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0271 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01517 | hp2 | a0002 | c0011 | t0001 | g0223 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01884 | hp2 | a0001 | c0004 | t0003 | g0333 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01891 | hp2 | a0003 | c0006 | t0002 | g0351 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01928 | hp2 | a0002 | c0008 | t0002 | g0039 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01943 | hp2 | a0001 | c0001 | t0011 | g0122 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01978 | hp1 | a0007 | c0012 | t0001 | g0302 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0272 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG01981 | hp2 | a0002 | c0003 | t0003 | g0054 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0279 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02015 | hp1 | a0001 | c0005 | t0005 | g0230 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02015 | hp2 | a0001 | c0005 | t0003 | g0036 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02027 | hp2 | a0001 | c0013 | t0002 | g0273 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02055 | hp2 | a0001 | c0004 | t0004 | g0344 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02074 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02080 | hp1 | a0005 | c0009 | t0001 | g0070 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02083 | hp1 | a0012 | c0023 | t0003 | g0002 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02129 | hp1 | a0005 | c0009 | t0001 | g0073 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02132 | hp2 | a0005 | c0009 | t0001 | g0072 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02145 | hp1 | a0019 | c0037 | t0004 | g0016 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | CDX | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02165 | hp2 | a0001 | c0005 | t0003 | g0349 | EAS | CDX | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02257 | hp1 | a0001 | c0004 | t0003 | g0326 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02257 | hp2 | a0003 | c0007 | t0004 | g0320 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02258 | hp1 | a0001 | c0032 | t0003 | g0343 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02258 | hp2 | a0001 | c0004 | t0004 | g0328 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02280 | hp2 | a0003 | c0006 | t0002 | g0357 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02293 | hp1 | a0003 | c0006 | t0002 | g0350 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02300 | hp2 | a0002 | c0003 | t0003 | g0065 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02451 | hp1 | a0002 | c0003 | t0003 | g0220 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02523 | hp1 | a0007 | c0029 | t0003 | g0348 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02523 | hp2 | a0007 | c0012 | t0001 | g0299 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02572 | hp1 | a0001 | c0005 | t0003 | g0083 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02572 | hp2 | a0004 | c0015 | t0004 | g0289 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0265 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02615 | hp1 | a0003 | c0007 | t0004 | g0315 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02615 | hp2 | a0002 | c0003 | t0003 | g0215 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02622 | hp2 | a0004 | c0010 | t0001 | g0297 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02630 | hp1 | a0003 | c0006 | t0002 | g0352 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02630 | hp2 | a0003 | c0035 | t0001 | g0355 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02647 | hp1 | a0008 | c0019 | t0001 | g0330 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02647 | hp2 | a0003 | c0007 | t0004 | g0314 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02683 | hp1 | a0003 | c0006 | t0002 | g0358 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02683 | hp2 | a0002 | c0003 | t0003 | g0022 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0284 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02723 | hp1 | a0003 | c0007 | t0008 | g0306 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02723 | hp2 | a0004 | c0015 | t0002 | g0291 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02809 | hp1 | a0001 | c0004 | t0003 | g0340 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02809 | hp2 | a0001 | c0005 | t0002 | g0077 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02818 | hp1 | a0003 | c0007 | t0004 | g0316 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02818 | hp2 | a0003 | c0007 | t0004 | g0321 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0234 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02886 | hp2 | a0003 | c0007 | t0004 | g0317 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02895 | hp2 | a0001 | c0005 | t0002 | g0079 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02896 | hp1 | a0001 | c0005 | t0002 | g0081 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0218 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02922 | hp1 | a0003 | c0007 | t0012 | g0318 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02922 | hp2 | a0004 | c0010 | t0001 | g0292 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02970 | hp1 | a0001 | c0004 | t0003 | g0325 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02970 | hp2 | a0003 | c0007 | t0008 | g0307 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02976 | hp1 | a0004 | c0010 | t0007 | g0294 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02976 | hp2 | a0001 | c0004 | t0003 | g0011 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03041 | hp1 | a0001 | c0004 | t0003 | g0331 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03041 | hp2 | a0001 | c0005 | t0002 | g0080 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03098 | hp1 | a0001 | c0004 | t0004 | g0341 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03098 | hp2 | a0001 | c0014 | t0003 | g0345 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03130 | hp1 | a0001 | c0004 | t0004 | g0336 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03130 | hp2 | a0002 | c0003 | t0003 | g0214 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03139 | hp1 | a0003 | c0006 | t0002 | g0311 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03195 | hp1 | a0001 | c0005 | t0002 | g0229 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0257 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03209 | hp1 | a0003 | c0006 | t0002 | g0310 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03225 | hp1 | a0001 | c0004 | t0004 | g0339 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03225 | hp2 | a0001 | c0005 | t0003 | g0082 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03453 | hp1 | a0001 | c0004 | t0003 | g0322 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03486 | hp2 | a0001 | c0004 | t0003 | g0335 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0017 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03516 | hp1 | a0004 | c0010 | t0007 | g0293 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03516 | hp2 | a0002 | c0003 | t0003 | g0221 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03540 | hp1 | a0001 | c0004 | t0003 | g0323 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03540 | hp2 | a0001 | c0004 | t0004 | g0338 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03579 | hp2 | a0008 | c0034 | t0003 | g0334 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03669 | hp1 | a0003 | c0006 | t0002 | g0360 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03669 | hp2 | a0002 | c0003 | t0003 | g0061 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03710 | hp1 | a0002 | c0003 | t0003 | g0055 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0277 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0240 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03942 | hp1 | a0002 | c0003 | t0003 | g0308 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04115 | hp2 | a0003 | c0006 | t0002 | g0361 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0259 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0127 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04199 | hp2 | a0001 | c0025 | t0001 | g0285 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04228 | hp1 | a0017 | c0030 | t0001 | g0087 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG04228 | hp2 | a0002 | c0003 | t0003 | g0059 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18522 | hp1 | a0001 | c0014 | t0003 | g0347 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18522 | hp2 | a0001 | c0004 | t0003 | g0011 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18612 | hp1 | a0002 | c0003 | t0003 | g0058 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18612 | hp2 | a0005 | c0009 | t0001 | g0075 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18747 | hp1 | a0002 | c0011 | t0001 | g0057 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18747 | hp2 | a0001 | c0005 | t0003 | g0144 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18906 | hp1 | a0001 | c0004 | t0003 | g0342 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0224 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18941 | hp1 | a0002 | c0003 | t0003 | g0046 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18942 | hp2 | a0002 | c0008 | t0002 | g0041 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18943 | hp1 | a0005 | c0009 | t0001 | g0164 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18943 | hp2 | a0002 | c0003 | t0003 | g0056 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18944 | hp2 | a0002 | c0003 | t0003 | g0030 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18945 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18946 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18949 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18950 | hp1 | a0002 | c0003 | t0002 | g0040 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18950 | hp2 | a0020 | c0036 | t0002 | g0060 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18951 | hp1 | a0001 | c0017 | t0001 | g0208 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18952 | hp1 | a0002 | c0003 | t0003 | g0026 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18961 | hp1 | a0002 | c0003 | t0003 | g0069 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18969 | hp1 | a0002 | c0003 | t0005 | g0062 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18970 | hp1 | a0002 | c0003 | t0003 | g0051 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18972 | hp1 | a0002 | c0003 | t0005 | g0050 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18973 | hp1 | a0002 | c0003 | t0003 | g0038 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18978 | hp1 | a0015 | c0024 | t0002 | g0267 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18978 | hp2 | a0002 | c0003 | t0003 | g0031 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18980 | hp2 | a0002 | c0003 | t0003 | g0045 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18983 | hp2 | a0002 | c0008 | t0002 | g0053 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18984 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18984 | hp2 | a0002 | c0008 | t0002 | g0044 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18985 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18989 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18991 | hp2 | a0002 | c0008 | t0002 | g0067 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18994 | hp1 | a0002 | c0003 | t0003 | g0049 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19000 | hp1 | a0002 | c0003 | t0003 | g0052 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19002 | hp2 | a0001 | c0013 | t0006 | g0020 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19030 | hp2 | a0001 | c0005 | t0003 | g0084 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19054 | hp1 | a0002 | c0008 | t0002 | g0068 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19056 | hp1 | a0002 | c0003 | t0002 | g0035 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19058 | hp1 | a0018 | c0022 | t0002 | g0283 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19058 | hp2 | a0013 | c0028 | t0001 | g0147 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19062 | hp2 | a0002 | c0003 | t0003 | g0028 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19064 | hp2 | a0001 | c0017 | t0001 | g0203 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19065 | hp1 | a0001 | c0005 | t0006 | g0089 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19066 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19068 | hp2 | a0002 | c0008 | t0002 | g0034 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19072 | hp1 | a0002 | c0008 | t0002 | g0042 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19074 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19075 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19079 | hp1 | a0002 | c0003 | t0005 | g0043 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19081 | hp1 | a0002 | c0003 | t0003 | g0027 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19081 | hp2 | a0002 | c0003 | t0003 | g0047 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19083 | hp1 | a0002 | c0003 | t0003 | g0033 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19083 | hp2 | a0002 | c0011 | t0001 | g0149 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19085 | hp1 | a0002 | c0003 | t0003 | g0066 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19087 | hp1 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19090 | hp2 | a0001 | c0013 | t0002 | g0019 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19240 | hp1 | a0001 | c0004 | t0004 | g0327 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA19240 | hp2 | a0002 | c0003 | t0003 | g0217 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20129 | hp1 | a0001 | c0004 | t0004 | g0337 | AFR | ASW | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20129 | hp2 | a0004 | c0015 | t0004 | g0288 | AFR | ASW | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20752 | hp1 | a0010 | c0021 | t0001 | g0007 | EUR | TSI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20905 | hp1 | a0002 | c0003 | t0003 | g0064 | SAS | GIH | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20905 | hp2 | a0003 | c0006 | t0002 | g0353 | SAS | GIH | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02486 | hp1 | a0001 | c0005 | t0002 | g0078 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02486 | hp2 | a0001 | c0004 | t0004 | g0329 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG02559 | hp2 | a0003 | c0007 | t0004 | g0319 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03471 | hp1 | a0003 | c0007 | t0004 | g0313 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG03471 | hp2 | a0001 | c0004 | t0003 | g0324 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG06807 | hp1 | a0001 | c0005 | t0003 | g0085 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
HG06807 | hp2 | a0008 | c0019 | t0001 | g0332 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA18955 | hp2 | a0002 | c0008 | t0002 | g0048 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA20300 | hp2 | a0016 | c0026 | t0002 | g0290 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA21309 | hp1 | a0004 | c0010 | t0001 | g0295 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
NA21309 | hp2 | a0006 | c0020 | t0001 | g0193 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0305 | REF | REF | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0211 | REF | REF | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27500978 | C | T | 3 | a0006a0019a0020 | 7 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
missense_variant | MODERATE | c.154C>T | p.Arg52Trp | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/19 | 220/2776 | 154/1668 | 52/555 | chr8 | 27500978 | ||
chr8:27500979 | G | A | 1 | a0010 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.155G>A | p.Arg52Gln | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/19 | 221/2776 | 155/1668 | 52/555 | chr8 | 27500979 | ||
chr8:27500988 | A | G | 1 | a0003 | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
missense_variant | MODERATE | c.164A>G | p.Lys55Arg | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/19 | 230/2776 | 164/1668 | 55/555 | chr8 | 27500988 | ||
chr8:27503683 | A | G | 1 | a0008 | 3 | HG02647.hp1 HG03579.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.266A>G | p.Lys89Arg | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/19 | 332/2776 | 266/1668 | 89/555 | chr8 | 27503683 | ||
chr8:27503724 | C | T | 3 | a0004a0011a0019 | 12 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(9): Show |
missense_variant | MODERATE | c.307C>T | p.Arg103Cys | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/19 | 373/2776 | 307/1668 | 103/555 | chr8 | 27503724 | ||
chr8:27504998 | G | A | 1 | a0011 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.389G>A | p.Arg130His | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/19 | 455/2776 | 389/1668 | 130/555 | chr8 | 27504998 | ||
chr8:27505070 | G | A | 1 | a0005 | 7 | HG00597.hp2 HG00621.hp2 HG02080.hp1 others(4): Show |
missense_variant | MODERATE | c.461G>A | p.Cys154Tyr | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/19 | 527/2776 | 461/1668 | 154/555 | chr8 | 27505070 | ||
chr8:27515778 | G | A | 1 | a0018 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.796G>A | p.Gly266Arg | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/19 | 862/2776 | 796/1668 | 266/555 | chr8 | 27515778 | ||
chr8:27516348 | G | A | 3 | a0002a0012a0020 | 64 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
missense_variant | MODERATE | c.860G>A | p.Arg287Gln | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/19 | 926/2776 | 860/1668 | 287/555 | chr8 | 27516348 | ||
chr8:27525384 | C | T | 1 | a0017 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1081C>T | p.Pro361Ser | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/19 | 1147/2776 | 1081/1668 | 361/555 | chr8 | 27525384 | ||
chr8:27525432 | G | A | 1 | a0009 | 2 | HG00639.hp1 HG01109.hp1 |
missense_variant | MODERATE | c.1129G>A | p.Ala377Thr | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/19 | 1195/2776 | 1129/1668 | 377/555 | chr8 | 27525432 | ||
chr8:27536817 | A | AGTC | 2 | a0007a0009 | 6 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(3): Show |
disruptive_inframe_insertion | MODERATE | c.1206_1208dupTCG | p.Arg403dup | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1275/2776 | 1209/1668 | 403/555 | INFO_REALIGN_3_PRIME | chr8 | 27536817 | |
chr8:27536833 | G | A | 1 | a0012 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.1220G>A | p.Ser407Asn | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1286/2776 | 1220/1668 | 407/555 | chr8 | 27536833 | ||
chr8:27536833 | G | T | 1 | a0013 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1220G>T | p.Ser407Ile | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1286/2776 | 1220/1668 | 407/555 | chr8 | 27536833 | ||
chr8:27540575 | C | T | 1 | a0014 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1298C>T | p.Pro433Leu | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/19 | 1364/2776 | 1298/1668 | 433/555 | chr8 | 27540575 | ||
chr8:27541502 | A | G | 1 | a0016 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1409A>G | p.Glu470Gly | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/19 | 1475/2776 | 1409/1668 | 470/555 | chr8 | 27541502 | ||
chr8:27543777 | C | A | 1 | a0015 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.1478C>A | p.Ala493Glu | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/19 | 1544/2776 | 1478/1668 | 493/555 | chr8 | 27543777 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27505098 | T | A | 1 | a0001c0017 | 2 | NA18951.hp1 NA19064.hp2 |
synonymous_variant | LOW | c.489T>A | p.Pro163Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/19 | 555/2776 | 489/1668 | 163/555 | chr8 | 27505098 | ||
chr8:27506925 | A | C | 5 | a0001c0004a0001c0014a0001c0032others(2): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
synonymous_variant | LOW | c.591A>C | p.Gly197Gly | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/19 | 657/2776 | 591/1668 | 197/555 | chr8 | 27506925 | ||
chr8:27511862 | G | A | 1 | a0001c0014 | 3 | HG01243.hp2 HG03098.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.687G>A | p.Pro229Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/19 | 753/2776 | 687/1668 | 229/555 | chr8 | 27511862 | ||
chr8:27515753 | C | T | 1 | a0006c0016 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp1 |
synonymous_variant | LOW | c.771C>T | p.Ser257Ser | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/19 | 837/2776 | 771/1668 | 257/555 | chr8 | 27515753 | ||
chr8:27516337 | G | A | 1 | a0009c0018 | 2 | HG00639.hp1 HG01109.hp1 |
synonymous_variant | LOW | c.849G>A | p.Gln283Gln | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/19 | 915/2776 | 849/1668 | 283/555 | chr8 | 27516337 | ||
chr8:27518048 | A | G | 1 | a0009c0018 | 2 | HG00639.hp1 HG01109.hp1 |
synonymous_variant | LOW | c.921A>G | p.Glu307Glu | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/19 | 987/2776 | 921/1668 | 307/555 | chr8 | 27518048 | ||
chr8:27522443 | C | T | 1 | a0001c0013 | 3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
synonymous_variant | LOW | c.993C>T | p.Phe331Phe | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/19 | 1059/2776 | 993/1668 | 331/555 | chr8 | 27522443 | ||
chr8:27522497 | C | T | 1 | a0001c0031 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.1047C>T | p.Pro349Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/19 | 1113/2776 | 1047/1668 | 349/555 | chr8 | 27522497 | ||
chr8:27525365 | G | A | 1 | a0001c0032 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1062G>A | p.Ala354Ala | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/19 | 1128/2776 | 1062/1668 | 354/555 | chr8 | 27525365 | ||
chr8:27536849 | C | T | 1 | a0003c0006 | 13 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(10): Show |
synonymous_variant | LOW | c.1236C>T | p.Ser412Ser | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1302/2776 | 1236/1668 | 412/555 | chr8 | 27536849 | ||
chr8:27538691 | G | A | 7 | a0001c0002a0001c0025a0002c0008others(4): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
splice_region_variant&synonymous_variant | LOW | c.1275G>A | p.Ala425Ala | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/19 | 1341/2776 | 1275/1668 | 425/555 | chr8 | 27538691 | ||
chr8:27544447 | A | C | 20 | a0001c0002a0001c0004a0001c0005others(17): Show | 198 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
synonymous_variant | LOW | c.1593A>C | p.Pro531Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 1659/2776 | 1593/1668 | 531/555 | chr8 | 27544447 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27491156 | C | T | 1 | a0003c0007t0008 | 2 | HG02723.hp1 HG02970.hp2 |
5_prime_UTR_variant | MODIFIER | c.-53C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/19 | 53 | chr8 | 27491156 | |||||
chr8:27544557 | A | G | 31 | a0001c0001t0006a0001c0002t0002a0001c0004t0003others(28): Show | 199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*35A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 35 | chr8 | 27544557 | |||||
chr8:27544615 | T | C | 26 | a0001c0002t0002a0001c0004t0003a0001c0004t0004others(23): Show | 193 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*93T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 93 | chr8 | 27544615 | |||||
chr8:27544736 | G | A | 2 | a0003c0007t0008a0003c0007t0012 | 3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*214G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 214 | chr8 | 27544736 | |||||
chr8:27544750 | G | A | 1 | a0001c0001t0009 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 228 | chr8 | 27544750 | |||||
chr8:27544802 | G | A | 1 | a0001c0001t0010 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 280 | chr8 | 27544802 | |||||
chr8:27544977 | C | T | 18 | a0001c0002t0002a0001c0004t0004a0001c0005t0002others(15): Show | 121 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*455C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 455 | chr8 | 27544977 | |||||
chr8:27545014 | G | A | 5 | a0001c0004t0004a0003c0007t0004a0004c0015t0004others(2): Show | 22 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 492 | chr8 | 27545014 | |||||
chr8:27545147 | G | A | 13 | a0001c0002t0002a0001c0005t0002a0001c0013t0002others(10): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 625 | chr8 | 27545147 | |||||
chr8:27545260 | G | A | 8 | a0001c0004t0003a0001c0005t0003a0001c0014t0003others(5): Show | 71 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*738G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 738 | chr8 | 27545260 | |||||
chr8:27545497 | G | T | 5 | a0001c0004t0004a0003c0007t0004a0004c0015t0004others(2): Show | 22 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*975G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 975 | chr8 | 27545497 | |||||
chr8:27545512 | A | G | 1 | a0001c0001t0011 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*990A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 990 | chr8 | 27545512 | |||||
chr8:27545536 | G | C | 1 | a0004c0010t0007 | 2 | HG02976.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1014G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 1014 | chr8 | 27545536 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27491377 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.101+68A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491377 | ||||||
chr8:27491447 | C | G | 12 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(9): Show | 12 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+138C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491447 | ||||||
chr8:27491849 | A | T | 2 | a0001c0005t0003g0349a0007c0029t0003g0348 | 2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.101+540A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491849 | ||||||
chr8:27491883 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.101+574T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491883 | ||||||
chr8:27491920 | A | G | 27 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(24): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.101+611A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491920 | ||||||
chr8:27491952 | G | GT | 30 | a0001c0001t0001g0309a0001c0004t0004g0344a0001c0014t0003g0345others(27): Show | 30 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.101+655dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27491952 | |||||
chr8:27491952 | GT | G | 12 | a0001c0001t0001g0014a0001c0004t0003g0011a0001c0004t0003g0322others(9): Show | 13 | HG00738.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.101+655delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27491952 | |||||
chr8:27491966 | T | G | 1 | a0003c0006t0002g0350 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101+657T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491966 | ||||||
chr8:27492019 | G | A | 2 | a0001c0002t0002g0017a0001c0002t0002g0018 | 2 | HG03490.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.101+710G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492019 | ||||||
chr8:27492189 | G | T | 1 | a0019c0037t0004g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101+880G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492189 | ||||||
chr8:27492271 | A | G | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+962A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492271 | ||||||
chr8:27492321 | T | C | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+1012T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492321 | ||||||
chr8:27492561 | A | C | 2 | a0001c0004t0003g0342a0001c0032t0003g0343 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.101+1252A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492561 | ||||||
chr8:27492587 | C | T | 1 | a0003c0007t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101+1278C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492587 | ||||||
chr8:27492597 | G | A | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+1288G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492597 | ||||||
chr8:27492739 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101+1430G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492739 | ||||||
chr8:27492814 | G | A | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.101+1505G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492814 | ||||||
chr8:27492883 | C | T | 1 | a0001c0001t0001g0305 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.101+1574C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492883 | ||||||
chr8:27493047 | G | A | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+1738G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493047 | ||||||
chr8:27493089 | A | C | 1 | a0001c0001t0001g0304 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.101+1780A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493089 | ||||||
chr8:27493117 | C | G | 5 | a0007c0012t0001g0299a0007c0012t0001g0301a0007c0012t0001g0302others(2): Show | 5 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1808C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493117 | ||||||
chr8:27493209 | G | A | 6 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+1900G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493209 | ||||||
chr8:27493464 | T | C | 2 | a0002c0003t0003g0022a0002c0003t0003g0023 | 2 | HG00140.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.101+2155T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493464 | ||||||
chr8:27493502 | G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.101+2193G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493502 | ||||||
chr8:27493648 | G | C | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+2339G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493648 | ||||||
chr8:27493702 | T | TG | 131 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(128): Show | 134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.101+2396dupG | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27493702 | |||||
chr8:27493881 | G | A | 1 | a0002c0003t0003g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.101+2572G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493881 | ||||||
chr8:27493994 | C | T | 1 | a0001c0005t0002g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.101+2685C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493994 | ||||||
chr8:27494081 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.101+2772A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494081 | ||||||
chr8:27494165 | T | A | 2 | a0003c0006t0002g0351a0003c0006t0002g0352 | 2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.101+2856T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494165 | ||||||
chr8:27494181 | T | C | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101+2872T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494181 | ||||||
chr8:27494221 | G | A | 52 | a0001c0005t0003g0036a0002c0003t0002g0035a0002c0003t0002g0040others(49): Show | 56 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.101+2912G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494221 | ||||||
chr8:27494290 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.101+2981C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494290 | ||||||
chr8:27494291 | G | T | 2 | a0001c0014t0003g0346a0001c0014t0003g0347 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.101+2982G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494291 | ||||||
chr8:27494420 | A | G | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+3111A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494420 | ||||||
chr8:27494473 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.101+3164C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494473 | ||||||
chr8:27494474 | T | G | 3 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028 | 3 | NA18952.hp1 NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.101+3165T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494474 | ||||||
chr8:27494506 | A | G | 2 | a0001c0005t0003g0349a0007c0029t0003g0348 | 2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.101+3197A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494506 | ||||||
chr8:27494633 | T | C | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+3324T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494633 | ||||||
chr8:27494714 | T | C | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+3405T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494714 | ||||||
chr8:27494727 | G | A | 6 | a0005c0009t0001g0070a0005c0009t0001g0071a0005c0009t0001g0072others(3): Show | 6 | HG00597.hp2 HG00621.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+3418G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494727 | ||||||
chr8:27494741 | G | T | 1 | a0003c0007t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101+3432G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494741 | ||||||
chr8:27494801 | A | T | 1 | a0001c0004t0004g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.101+3492A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494801 | ||||||
chr8:27494815 | G | A | 1 | a0003c0006t0002g0353 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101+3506G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494815 | ||||||
chr8:27494944 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.101+3635G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494944 | ||||||
chr8:27495116 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.101+3807A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495116 | ||||||
chr8:27495233 | A | G | 63 | a0001c0002t0002g0218a0001c0002t0002g0219a0001c0002t0002g0224others(60): Show | 67 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.101+3924A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495233 | ||||||
chr8:27495250 | T | A | 1 | a0011c0033t0004g0015 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.101+3941T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495250 | ||||||
chr8:27495251 | C | T | 1 | a0011c0033t0004g0015 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.101+3942C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495251 | ||||||
chr8:27495304 | A | T | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+3995A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495304 | ||||||
chr8:27495326 | A | T | 5 | a0003c0007t0004g0316a0003c0007t0004g0317a0003c0007t0004g0319others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4017A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495326 | ||||||
chr8:27495373 | A | G | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+4064A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495373 | ||||||
chr8:27495546 | A | G | 3 | a0003c0006t0002g0350a0003c0006t0002g0360a0003c0006t0002g0361 | 3 | HG02293.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.101+4237A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495546 | ||||||
chr8:27495556 | G | A | 2 | a0002c0003t0003g0214a0002c0003t0003g0215 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.101+4247G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495556 | ||||||
chr8:27495573 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.101+4264G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495573 | ||||||
chr8:27495710 | A | G | 9 | a0001c0001t0001g0012a0004c0010t0001g0292a0004c0010t0001g0295others(6): Show | 10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+4401A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495710 | ||||||
chr8:27495802 | A | C | 1 | a0016c0026t0002g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.101+4493A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495802 | ||||||
chr8:27495864 | G | C | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.101+4555G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495864 | ||||||
chr8:27495998 | C | T | 1 | a0003c0006t0002g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.101+4689C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495998 | ||||||
chr8:27496226 | C | A | 27 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(24): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.102-4700C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496226 | ||||||
chr8:27496346 | C | T | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.102-4580C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496346 | ||||||
chr8:27496620 | C | T | 1 | a0003c0007t0004g0320 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.102-4306C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496620 | ||||||
chr8:27496862 | T | C | 62 | a0001c0001t0001g0249a0001c0002t0002g0010a0001c0002t0002g0017others(59): Show | 63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.102-4064T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496862 | ||||||
chr8:27496901 | A | G | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.102-4025A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496901 | ||||||
chr8:27496948 | G | T | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.102-3978G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496948 | ||||||
chr8:27496954 | A | G | 131 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(128): Show | 134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.102-3972A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496954 | ||||||
chr8:27496983 | G | C | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.102-3943G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496983 | ||||||
chr8:27497072 | C | A | 6 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(3): Show | 6 | HG02055.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-3854C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497072 | ||||||
chr8:27497094 | T | C | 141 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(138): Show | 144 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.102-3832T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497094 | ||||||
chr8:27497184 | A | C | 1 | a0003c0006t0002g0353 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.102-3742A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497184 | ||||||
chr8:27497234 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.102-3692T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497234 | ||||||
chr8:27497404 | T | G | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.102-3522T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497404 | ||||||
chr8:27497421 | C | G | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.102-3505C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497421 | ||||||
chr8:27497518 | G | A | 6 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(3): Show | 7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-3408G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497518 | ||||||
chr8:27497613 | T | C | 131 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(128): Show | 134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.102-3313T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497613 | ||||||
chr8:27497622 | T | C | 1 | a0017c0030t0001g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102-3304T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497622 | ||||||
chr8:27497899 | C | T | 1 | a0001c0002t0002g0224 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.102-3027C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497899 | ||||||
chr8:27497948 | TCATTTAC others(13): Show |
T | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.102-2955_102-2936d others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27497948 | |||||
chr8:27498051 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.102-2875A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498051 | ||||||
chr8:27498251 | C | T | 1 | a0004c0010t0001g0298 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.102-2675C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498251 | ||||||
chr8:27498255 | G | A | 1 | a0001c0005t0002g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.102-2671G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498255 | ||||||
chr8:27498407 | C | T | 61 | a0001c0001t0001g0249a0001c0002t0002g0010a0001c0002t0002g0017others(58): Show | 62 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.102-2519C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498407 | ||||||
chr8:27498573 | G | T | 27 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(24): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.102-2353G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498573 | ||||||
chr8:27498960 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.102-1966G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498960 | ||||||
chr8:27498974 | T | G | 361 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(358): Show | 372 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(369): Show |
intron_variant | MODIFIER | c.102-1952T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498974 | ||||||
chr8:27499188 | A | T | 4 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1738A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499188 | ||||||
chr8:27499294 | C | A | 4 | a0001c0002t0002g0231a0001c0002t0002g0232a0001c0002t0002g0233others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1632C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499294 | ||||||
chr8:27499299 | G | C | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.102-1627G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499299 | ||||||
chr8:27499322 | A | G | 1 | a0003c0006t0002g0361 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.102-1604A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499322 | ||||||
chr8:27499502 | T | C | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.102-1424T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499502 | ||||||
chr8:27499762 | T | C | 14 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(11): Show | 14 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.102-1164T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499762 | ||||||
chr8:27499793 | G | A | 1 | a0001c0004t0003g0322 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102-1133G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499793 | ||||||
chr8:27499840 | G | GTTC | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.102-1084_102-1082d others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27499840 | |||||
chr8:27499895 | C | A | 1 | a0016c0026t0002g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.102-1031C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499895 | ||||||
chr8:27500177 | C | T | 13 | a0001c0001t0001g0012a0004c0010t0001g0292a0004c0010t0001g0295others(10): Show | 14 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.102-749C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500177 | ||||||
chr8:27500616 | G | A | 1 | a0003c0007t0008g0306 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102-310G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500616 | ||||||
chr8:27500768 | C | T | 1 | a0003c0007t0004g0319 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102-158C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500768 | ||||||
chr8:27500770 | C | T | 16 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(13): Show | 16 | HG00423.hp1 HG01496.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.102-156C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500770 | ||||||
chr8:27500852 | T | C | 5 | a0001c0002t0002g0235a0001c0002t0002g0236a0001c0002t0002g0237others(2): Show | 5 | NA18946.hp1 NA18954.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-74T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500852 | ||||||
chr8:27501124 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.186+114C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501124 | ||||||
chr8:27501277 | C | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.186+267C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501277 | ||||||
chr8:27501280 | C | T | 1 | a0001c0005t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.186+270C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501280 | ||||||
chr8:27501324 | T | C | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.186+314T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501324 | ||||||
chr8:27501324 | T | TTTC | 41 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0001g0135others(38): Show | 41 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.186+383_186+385dup others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | T | TTTCTTC | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0123others(24): Show | 29 | HG00597.hp1 HG00621.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.186+380_186+385dup others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | T | TTTCTTCT others(2): Show |
17 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(14): Show | 17 | HG00544.hp2 HG00735.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.186+377_186+385dup others(9): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | T | TTTCTTCT others(5): Show |
12 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(9): Show | 12 | HG01261.hp1 HG02280.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+374_186+385dup others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | T | TTTCTTCT others(8): Show |
7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG01106.hp2 HG02055.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+371_186+385dup others(15): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | T | TTTCTTCT others(11): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02083.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.186+368_186+385dup others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | T | TTTCTTCT others(14): Show |
7 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | HG02735.hp1 HG02735.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+365_186+385dup others(21): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTC | T | 43 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(40): Show | 46 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.186+383_186+385del others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTCTTC | T | 37 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(34): Show | 39 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.186+380_186+385del others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTCTTCT others(2): Show |
T | 47 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0088others(44): Show | 48 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.186+377_186+385del others(9): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTCTTCT others(5): Show |
T | 16 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0188others(13): Show | 17 | HG00323.hp1 HG00609.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.186+374_186+385del others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTCTTCT others(8): Show |
T | 5 | a0001c0002t0002g0010a0001c0005t0003g0085a0001c0031t0001g0191others(2): Show | 6 | HG00408.hp1 HG00733.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+371_186+385del others(15): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTCTTCT others(11): Show |
T | 3 | a0001c0001t0001g0192a0001c0002t0002g0284a0001c0025t0001g0285 | 3 | HG02698.hp1 HG03139.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.186+368_186+385del others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTCTTCT others(14): Show |
T | 3 | a0001c0001t0001g0194a0001c0002t0002g0286a0006c0020t0001g0193 | 3 | HG01891.hp1 NA18947.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.186+365_186+385del others(21): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501324 | TTTCTTCT others(17): Show |
T | 1 | a0004c0010t0001g0298 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.186+362_186+385del others(24): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | |||||
chr8:27501331 | T | C | 1 | a0001c0005t0006g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.186+321T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501331 | ||||||
chr8:27501363 | C | T | 1 | a0001c0002t0002g0287 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.186+353C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501363 | ||||||
chr8:27501380 | T | TC | 5 | a0003c0006t0002g0311a0003c0006t0002g0351a0003c0006t0002g0354others(2): Show | 5 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+371dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501380 | |||||
chr8:27501381 | C | CTTTCTTC others(99): Show |
1 | a0001c0001t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.186+373_186+374ins others(106): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501381 | |||||
chr8:27501382 | T | TTCTTCTT others(71): Show |
2 | a0001c0013t0002g0019a0001c0013t0006g0020 | 2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.186+385_186+386ins others(78): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501382 | |||||
chr8:27501382 | T | TTCTTCTT others(76): Show |
1 | a0001c0001t0001g0021 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(83): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501382 | |||||
chr8:27501383 | T | TC | 6 | a0003c0006t0002g0352a0003c0006t0002g0356a0003c0006t0002g0360others(3): Show | 6 | HG01167.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+374dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501383 | |||||
chr8:27501387 | C | CCTTCT | 5 | a0003c0006t0002g0311a0003c0006t0002g0350a0003c0006t0002g0358others(2): Show | 5 | HG00733.hp1 HG02257.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+377_186+378ins others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501387 | ||||||
chr8:27501387 | C | CCTTCTTC others(5): Show |
3 | a0003c0006t0002g0357a0003c0007t0004g0313a0003c0007t0004g0317 | 3 | HG02280.hp2 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.186+377_186+378ins others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501387 | ||||||
chr8:27501387 | C | CT | 4 | a0001c0001t0001g0172a0001c0001t0001g0187a0007c0012t0001g0302others(1): Show | 4 | HG00639.hp1 HG01978.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+379dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTCCT others(178): Show |
1 | a0001c0001t0001g0091 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.186+381_186+382ins others(185): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTTCT | 3 | a0001c0001t0001g0207a0001c0002t0002g0234a0001c0017t0001g0208 | 3 | HG02886.hp1 NA18951.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.186+401_186+407dup others(7): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTTCT others(174): Show |
1 | a0001c0001t0001g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.186+384_186+385ins others(181): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTTCT others(3): Show |
1 | a0001c0001t0001g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTTCT others(6): Show |
2 | a0001c0005t0003g0349a0001c0017t0001g0203 | 2 | HG02165.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.186+385_186+386ins others(13): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTTCT others(9): Show |
3 | a0001c0001t0001g0200a0007c0012t0001g0299a0007c0029t0003g0348 | 3 | HG02523.hp1 HG02523.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.186+385_186+386ins others(16): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTTCT others(179): Show |
1 | a0001c0001t0006g0093 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(186): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501387 | C | CTTCTTCT others(99): Show |
1 | a0001c0001t0001g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(106): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | |||||
chr8:27501389 | T | C | 8 | a0003c0006t0002g0311a0003c0006t0002g0350a0003c0006t0002g0357others(5): Show | 8 | HG00733.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+379T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501389 | ||||||
chr8:27501389 | T | TC | 6 | a0003c0006t0002g0352a0003c0006t0002g0356a0003c0006t0002g0360others(3): Show | 6 | HG01167.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+380dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | |||||
chr8:27501389 | T | TCCTTCTT others(8): Show |
4 | a0003c0006t0002g0310a0003c0007t0004g0314a0003c0007t0004g0315others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+380_186+381ins others(15): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | |||||
chr8:27501389 | T | TCTCCTTC others(199): Show |
1 | a0001c0001t0001g0090 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.186+381_186+382ins others(206): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | |||||
chr8:27501389 | T | TCTTCTTC others(14): Show |
1 | a0003c0007t0012g0318 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(21): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | |||||
chr8:27501389 | T | TCTTCTTC others(17): Show |
1 | a0003c0007t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(24): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | |||||
chr8:27501394 | T | C | 1 | a0003c0006t0002g0351 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+384T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501394 | ||||||
chr8:27501394 | T | TGCTTCTG others(100): Show |
1 | a0001c0014t0003g0346 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186+384_186+385ins others(107): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501394 | ||||||
chr8:27501394 | T | TTCTGCTT others(103): Show |
1 | a0001c0014t0003g0347 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(110): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501394 | |||||
chr8:27501395 | T | TCTTCTTC others(6): Show |
1 | a0001c0002t0002g0240 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(13): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501395 | ||||||
chr8:27501396 | T | C | 23 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(20): Show | 23 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.186+386T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501396 | ||||||
chr8:27501401 | T | C | 1 | a0003c0006t0002g0351 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+391T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501401 | ||||||
chr8:27501403 | T | C | 8 | a0003c0006t0002g0350a0003c0006t0002g0353a0003c0006t0002g0356others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.186+393T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501403 | ||||||
chr8:27501410 | T | C | 1 | a0003c0006t0002g0351 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+400T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501410 | ||||||
chr8:27501411 | C | CTTCT | 21 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(18): Show | 21 | HG00733.hp1 HG01106.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.186+404_186+407dup others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501411 | |||||
chr8:27501411 | C | T | 1 | a0003c0006t0002g0351 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+401C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501411 | ||||||
chr8:27501418 | T | C | 2 | a0001c0014t0003g0346a0001c0014t0003g0347 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.186+408T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501418 | ||||||
chr8:27501420 | C | T | 2 | a0001c0014t0003g0346a0001c0014t0003g0347 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.186+410C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501420 | ||||||
chr8:27501421 | T | C | 3 | a0001c0001t0001g0151a0001c0014t0003g0346a0001c0014t0003g0347 | 3 | HG01243.hp2 NA18522.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.186+411T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501421 | ||||||
chr8:27501613 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.186+603G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501613 | ||||||
chr8:27501654 | A | T | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.186+644A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501654 | ||||||
chr8:27501776 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.186+766G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501776 | ||||||
chr8:27501849 | A | G | 1 | a0001c0014t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186+839A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501849 | ||||||
chr8:27501869 | T | C | 1 | a0020c0036t0002g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.186+859T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501869 | ||||||
chr8:27501906 | TA | T | 18 | a0001c0004t0004g0344a0001c0005t0002g0077a0001c0005t0002g0078others(15): Show | 18 | HG00597.hp2 HG00621.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.186+906delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501906 | |||||
chr8:27501978 | A | C | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+968A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501978 | ||||||
chr8:27502084 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.186+1074C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502084 | ||||||
chr8:27502090 | C | G | 2 | a0004c0010t0001g0297a0004c0010t0001g0298 | 2 | HG00639.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.186+1080C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502090 | ||||||
chr8:27502103 | C | T | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+1093C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502103 | ||||||
chr8:27502197 | C | T | 1 | a0003c0006t0002g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.186+1187C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502197 | ||||||
chr8:27502239 | A | G | 9 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+1229A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502239 | ||||||
chr8:27502247 | C | T | 2 | a0002c0003t0003g0216a0002c0003t0003g0217 | 2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.186+1237C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502247 | ||||||
chr8:27502268 | A | G | 1 | a0003c0007t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186+1258A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502268 | ||||||
chr8:27502455 | T | C | 27 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(24): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.187-1149T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502455 | ||||||
chr8:27502896 | G | A | 1 | a0006c0020t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187-708G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502896 | ||||||
chr8:27502972 | C | T | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-632C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502972 | ||||||
chr8:27503051 | G | T | 27 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(24): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.187-553G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503051 | ||||||
chr8:27503073 | G | A | 2 | a0004c0015t0004g0288a0004c0015t0004g0289 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.187-531G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503073 | ||||||
chr8:27503147 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.187-457G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503147 | ||||||
chr8:27503283 | T | G | 1 | a0016c0026t0002g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.187-321T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503283 | ||||||
chr8:27503404 | G | T | 1 | a0001c0001t0006g0093 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.187-200G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503404 | ||||||
chr8:27503448 | A | C | 27 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(24): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.187-156A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503448 | ||||||
chr8:27503530 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.187-74G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503530 | ||||||
chr8:27503794 | C | T | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.346+31C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503794 | ||||||
chr8:27503812 | C | T | 13 | a0001c0001t0001g0012a0004c0010t0001g0292a0004c0010t0001g0295others(10): Show | 14 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+49C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503812 | ||||||
chr8:27503835 | T | C | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.346+72T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503835 | ||||||
chr8:27503872 | C | T | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.346+109C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503872 | ||||||
chr8:27503873 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.346+110G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503873 | ||||||
chr8:27503899 | C | A | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.346+136C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503899 | ||||||
chr8:27503998 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.346+235T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503998 | ||||||
chr8:27504117 | G | T | 1 | a0007c0012t0001g0299 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.346+354G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27504117 | ||||||
chr8:27504245 | A | AC | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.346+482_346+483ins others(1): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27504245 | ||||||
chr8:27504625 | T | C | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.347-331T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27504625 | ||||||
chr8:27505171 | G | C | 27 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(24): Show | 28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.537+25G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505171 | ||||||
chr8:27505269 | C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0150 | 2 | NA18954.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.537+123C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505269 | ||||||
chr8:27505368 | A | C | 6 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(3): Show | 6 | HG02055.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+222A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505368 | ||||||
chr8:27505512 | C | T | 1 | a0003c0006t0002g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.537+366C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505512 | ||||||
chr8:27505601 | G | A | 2 | a0002c0011t0001g0222a0002c0011t0001g0223 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.537+455G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505601 | ||||||
chr8:27505619 | A | G | 118 | a0001c0001t0001g0021a0001c0001t0001g0249a0001c0002t0002g0010others(115): Show | 120 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.537+473A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505619 | ||||||
chr8:27505630 | T | C | 1 | a0001c0002t0002g0284 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.537+484T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505630 | ||||||
chr8:27505721 | G | C | 2 | a0005c0009t0001g0072a0005c0009t0001g0073 | 2 | HG02129.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.537+575G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505721 | ||||||
chr8:27505874 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.537+728A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505874 | ||||||
chr8:27505922 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.537+776A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505922 | ||||||
chr8:27506051 | C | T | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.538-821C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506051 | ||||||
chr8:27506096 | G | C | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.538-776G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506096 | ||||||
chr8:27506107 | G | A | 55 | a0001c0001t0001g0249a0001c0002t0002g0010a0001c0002t0002g0017others(52): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.538-765G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506107 | ||||||
chr8:27506330 | T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0135a0001c0001t0001g0154 | 3 | NA18960.hp1 NA18966.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.538-542T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506330 | ||||||
chr8:27506353 | G | T | 1 | a0004c0010t0001g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.538-519G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506353 | ||||||
chr8:27506795 | T | C | 1 | a0003c0035t0001g0355 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.538-77T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506795 | ||||||
chr8:27507270 | T | C | 326 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(323): Show | 336 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.660+276T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507270 | ||||||
chr8:27507358 | G | C | 1 | a0003c0007t0004g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.660+364G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507358 | ||||||
chr8:27507422 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.660+428C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507422 | ||||||
chr8:27507440 | G | A | 65 | a0001c0001t0001g0249a0001c0002t0002g0010a0001c0002t0002g0017others(62): Show | 66 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.660+446G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507440 | ||||||
chr8:27507447 | A | G | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+453A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507447 | ||||||
chr8:27507449 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.660+455C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507449 | ||||||
chr8:27507471 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.660+477G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507471 | ||||||
chr8:27507532 | G | A | 11 | a0001c0002t0002g0235a0001c0002t0002g0236a0001c0002t0002g0237others(8): Show | 11 | HG00438.hp1 HG03927.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+538G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507532 | ||||||
chr8:27507639 | A | G | 12 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(9): Show | 12 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.660+645A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507639 | ||||||
chr8:27507695 | T | A | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.660+701T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507695 | ||||||
chr8:27507751 | A | C | 52 | a0001c0001t0001g0249a0001c0002t0002g0010a0001c0002t0002g0017others(49): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.660+757A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507751 | ||||||
chr8:27507897 | C | T | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+903C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507897 | ||||||
chr8:27507913 | C | A | 144 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(141): Show | 147 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.660+919C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507913 | ||||||
chr8:27507985 | G | A | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+991G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507985 | ||||||
chr8:27508013 | G | A | 1 | a0002c0003t0003g0061 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.660+1019G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508013 | ||||||
chr8:27508131 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.660+1137G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508131 | ||||||
chr8:27508195 | C | T | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.660+1201C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508195 | ||||||
chr8:27508306 | A | AAAAC | 56 | a0001c0001t0001g0021a0001c0004t0003g0011a0001c0004t0003g0322others(53): Show | 57 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.660+1324_660+1327d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508306 | |||||
chr8:27508329 | T | G | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.660+1335T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508329 | ||||||
chr8:27508371 | T | C | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+1377T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508371 | ||||||
chr8:27508635 | T | G | 14 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(11): Show | 14 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.660+1641T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508635 | ||||||
chr8:27508659 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.660+1665G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508659 | ||||||
chr8:27508668 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.660+1674G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508668 | ||||||
chr8:27508699 | C | T | 1 | a0003c0006t0002g0352 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660+1705C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508699 | ||||||
chr8:27508735 | C | T | 2 | a0001c0013t0002g0019a0001c0013t0006g0020 | 2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.660+1741C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508735 | ||||||
chr8:27508769 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.660+1775C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508769 | ||||||
chr8:27508770 | G | A | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+1776G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508770 | ||||||
chr8:27508783 | T | C | 1 | a0003c0006t0002g0357 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.660+1789T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508783 | ||||||
chr8:27508814 | G | C | 1 | a0001c0014t0003g0346 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.660+1820G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508814 | ||||||
chr8:27508819 | C | T | 56 | a0001c0001t0001g0021a0001c0004t0003g0011a0001c0004t0003g0322others(53): Show | 57 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.660+1825C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508819 | ||||||
chr8:27508884 | G | C | 203 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(200): Show | 210 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.660+1890G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508884 | ||||||
chr8:27508890 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+1896C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508890 | ||||||
chr8:27508946 | C | CT | 63 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0021others(60): Show | 66 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.660+1979dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | |||||
chr8:27508946 | C | CTT | 6 | a0001c0001t0001g0177a0001c0001t0001g0185a0002c0011t0001g0223others(3): Show | 6 | HG01361.hp1 HG01517.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+1978_660+1979d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | |||||
chr8:27508946 | C | CTTT | 7 | a0001c0013t0006g0020a0003c0006t0002g0310a0003c0006t0002g0311others(4): Show | 7 | HG00733.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+1977_660+1979d others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | |||||
chr8:27508946 | CT | C | 28 | a0001c0001t0001g0188a0001c0002t0002g0247a0001c0002t0002g0255others(25): Show | 29 | HG00438.hp1 HG00609.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.660+1979delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | |||||
chr8:27508946 | CTT | C | 57 | a0001c0001t0001g0249a0001c0002t0002g0010a0001c0002t0002g0017others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.660+1978_660+1979d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | |||||
chr8:27509020 | G | A | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+2026G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509020 | ||||||
chr8:27509215 | G | T | 1 | a0003c0035t0001g0355 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.660+2221G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509215 | ||||||
chr8:27509399 | G | A | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+2405G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509399 | ||||||
chr8:27509452 | A | G | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-2384A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509452 | ||||||
chr8:27509576 | T | C | 6 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(3): Show | 7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.661-2260T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509576 | ||||||
chr8:27509623 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.661-2213C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509623 | ||||||
chr8:27509638 | C | G | 9 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-2198C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509638 | ||||||
chr8:27509659 | G | A | 1 | a0002c0003t0003g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-2177G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509659 | ||||||
chr8:27509755 | A | G | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.661-2081A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509755 | ||||||
chr8:27509792 | G | C | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-2044G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509792 | ||||||
chr8:27509972 | G | A | 1 | a0004c0010t0001g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.661-1864G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509972 | ||||||
chr8:27509984 | A | G | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-1852A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509984 | ||||||
chr8:27509998 | G | A | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-1838G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509998 | ||||||
chr8:27510010 | G | C | 2 | a0001c0014t0003g0346a0001c0014t0003g0347 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.661-1826G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510010 | ||||||
chr8:27510085 | A | C | 64 | a0001c0001t0001g0249a0001c0002t0002g0010a0001c0002t0002g0017others(61): Show | 65 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.661-1751A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510085 | ||||||
chr8:27510124 | T | G | 24 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(21): Show | 24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.661-1712T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510124 | ||||||
chr8:27510147 | A | G | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-1689A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510147 | ||||||
chr8:27510224 | G | A | 10 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-1612G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510224 | ||||||
chr8:27510257 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.661-1579A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510257 | ||||||
chr8:27510289 | G | A | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-1547G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510289 | ||||||
chr8:27510322 | G | A | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-1514G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510322 | ||||||
chr8:27510339 | C | G | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.661-1497C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510339 | ||||||
chr8:27510560 | T | A | 1 | a0002c0008t0002g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.661-1276T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510560 | ||||||
chr8:27510766 | C | T | 5 | a0003c0006t0002g0353a0003c0006t0002g0354a0003c0006t0002g0356others(2): Show | 5 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-1070C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510766 | ||||||
chr8:27510770 | A | G | 4 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1066A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510770 | ||||||
chr8:27510851 | A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0169 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.661-985A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510851 | ||||||
chr8:27510857 | G | A | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-979G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510857 | ||||||
chr8:27511061 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.661-775G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511061 | ||||||
chr8:27511118 | C | T | 3 | a0001c0001t0001g0021a0001c0013t0002g0019a0001c0013t0006g0020 | 3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-718C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511118 | ||||||
chr8:27511228 | C | T | 1 | a0003c0007t0004g0315 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.661-608C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511228 | ||||||
chr8:27511251 | G | A | 26 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-585G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511251 | ||||||
chr8:27511323 | G | A | 1 | a0002c0003t0005g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.661-513G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511323 | ||||||
chr8:27511488 | A | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0110 | 3 | NA18989.hp1 NA19000.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.661-348A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511488 | ||||||
chr8:27511674 | T | C | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-162T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511674 | ||||||
chr8:27511817 | A | G | 267 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0021others(264): Show | 275 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.661-19A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511817 | ||||||
chr8:27512065 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.735+155T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512065 | ||||||
chr8:27512100 | G | GA | 63 | a0001c0001t0001g0104a0001c0001t0001g0134a0001c0001t0001g0249others(60): Show | 64 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.735+208dupA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27512100 | |||||
chr8:27512100 | G | GAA | 6 | a0001c0001t0001g0021a0001c0002t0002g0231a0001c0002t0002g0242others(3): Show | 6 | HG01515.hp1 HG01517.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.735+207_735+208dup others(2): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27512100 | |||||
chr8:27512216 | G | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+306G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512216 | ||||||
chr8:27512272 | C | A | 1 | a0004c0010t0001g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.735+362C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512272 | ||||||
chr8:27512556 | C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.735+646C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512556 | ||||||
chr8:27512572 | C | G | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+662C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512572 | ||||||
chr8:27512785 | T | TTGGACAA others(324): Show |
1 | a0001c0002t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.735+889_735+890ins others(331): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27512785 | |||||
chr8:27512804 | C | T | 14 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(11): Show | 14 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.735+894C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512804 | ||||||
chr8:27512829 | C | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+919C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512829 | ||||||
chr8:27513058 | C | T | 1 | a0003c0007t0008g0307 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.735+1148C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513058 | ||||||
chr8:27513091 | G | A | 1 | a0003c0006t0002g0357 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.735+1181G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513091 | ||||||
chr8:27513221 | T | G | 10 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.735+1311T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513221 | ||||||
chr8:27513261 | G | A | 2 | a0002c0003t0003g0214a0002c0003t0003g0215 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.735+1351G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513261 | ||||||
chr8:27513323 | T | C | 11 | a0002c0003t0003g0049a0002c0008t0002g0034a0002c0008t0002g0039others(8): Show | 11 | HG01928.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+1413T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513323 | ||||||
chr8:27513406 | G | T | 5 | a0003c0007t0004g0316a0003c0007t0004g0317a0003c0007t0004g0319others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+1496G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513406 | ||||||
chr8:27513544 | A | C | 1 | a0001c0005t0003g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.735+1634A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513544 | ||||||
chr8:27513566 | C | T | 4 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028others(1): Show | 4 | NA18952.hp1 NA19062.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+1656C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513566 | ||||||
chr8:27513599 | C | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+1689C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513599 | ||||||
chr8:27513655 | C | G | 2 | a0004c0015t0004g0288a0004c0015t0004g0289 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.735+1745C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513655 | ||||||
chr8:27513684 | A | T | 6 | a0001c0002t0002g0246a0001c0002t0002g0250a0001c0002t0002g0253others(3): Show | 6 | NA18949.hp2 NA18956.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+1774A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513684 | ||||||
chr8:27513829 | G | C | 10 | a0003c0007t0004g0312a0003c0007t0004g0313a0003c0007t0004g0314others(7): Show | 10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-1889G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513829 | ||||||
chr8:27513923 | A | G | 3 | a0001c0004t0003g0340a0001c0004t0003g0342a0001c0032t0003g0343 | 3 | HG02258.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.736-1795A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513923 | ||||||
chr8:27513933 | C | G | 1 | a0001c0002t0002g0281 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.736-1785C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513933 | ||||||
chr8:27514029 | T | C | 133 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(130): Show | 136 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.736-1689T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514029 | ||||||
chr8:27514030 | C | T | 1 | a0003c0035t0001g0355 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.736-1688C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514030 | ||||||
chr8:27514060 | G | A | 77 | a0001c0001t0001g0012a0001c0001t0001g0249a0001c0002t0002g0010others(74): Show | 79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.736-1658G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514060 | ||||||
chr8:27514091 | G | A | 77 | a0001c0001t0001g0012a0001c0001t0001g0249a0001c0002t0002g0010others(74): Show | 79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.736-1627G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514091 | ||||||
chr8:27514095 | A | G | 77 | a0001c0001t0001g0012a0001c0001t0001g0249a0001c0002t0002g0010others(74): Show | 79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.736-1623A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514095 | ||||||
chr8:27514142 | A | AC | 11 | a0001c0001t0001g0226a0001c0005t0002g0077a0001c0005t0002g0078others(8): Show | 11 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.736-1570dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27514142 | |||||
chr8:27514167 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.736-1551G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514167 | ||||||
chr8:27514222 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.736-1496G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514222 | ||||||
chr8:27514222 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.736-1496G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514222 | ||||||
chr8:27514251 | G | A | 1 | a0002c0003t0003g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.736-1467G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514251 | ||||||
chr8:27514302 | G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0151 | 2 | NA18961.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.736-1416G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514302 | ||||||
chr8:27514309 | A | G | 2 | a0001c0014t0003g0346a0001c0014t0003g0347 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.736-1409A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514309 | ||||||
chr8:27514412 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.736-1306A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514412 | ||||||
chr8:27514629 | T | C | 2 | a0001c0002t0002g0218a0001c0002t0002g0219 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.736-1089T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514629 | ||||||
chr8:27514672 | G | A | 132 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0249others(129): Show | 135 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.736-1046G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514672 | ||||||
chr8:27514694 | A | G | 2 | a0001c0013t0002g0019a0001c0013t0006g0020 | 2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.736-1024A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514694 | ||||||
chr8:27514718 | C | T | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.736-1000C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514718 | ||||||
chr8:27515143 | G | A | 18 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(15): Show | 19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.736-575G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515143 | ||||||
chr8:27515189 | TC | T | 16 | a0001c0001t0001g0012a0003c0006t0002g0357a0003c0007t0004g0312others(13): Show | 17 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.736-525delC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27515189 | |||||
chr8:27515194 | G | GT | 4 | a0001c0001t0001g0200a0001c0002t0002g0237a0001c0002t0002g0258others(1): Show | 4 | HG00438.hp1 NA18941.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-517dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27515194 | |||||
chr8:27515201 | T | C | 16 | a0001c0001t0001g0012a0003c0006t0002g0357a0003c0007t0004g0312others(13): Show | 17 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.736-517T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515201 | ||||||
chr8:27515479 | AT | A | 18 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(15): Show | 19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.736-238delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515479 | ||||||
chr8:27515535 | TAGGTTGG others(15): Show |
T | 2 | a0002c0003t0003g0216a0002c0003t0003g0217 | 2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.736-180_736-159del others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27515535 | |||||
chr8:27515568 | A | C | 2 | a0002c0003t0003g0220a0002c0003t0003g0221 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.736-150A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515568 | ||||||
chr8:27515652 | G | A | 3 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020 | 3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.736-66G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515652 | ||||||
chr8:27515689 | C | A | 1 | a0016c0026t0002g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.736-29C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515689 | ||||||
chr8:27515892 | G | A | 6 | a0001c0002t0002g0259a0001c0002t0002g0262a0001c0002t0002g0266others(3): Show | 6 | HG00423.hp2 HG02040.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+79G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27515892 | ||||||
chr8:27515949 | G | A | 1 | a0001c0001t0001g0305 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.831+136G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27515949 | ||||||
chr8:27515960 | A | T | 1 | a0002c0008t0002g0042 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.831+147A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27515960 | ||||||
chr8:27515963 | C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0137 | 5 | HG01074.hp1 HG01257.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+150C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27515963 | ||||||
chr8:27516051 | G | A | 1 | a0003c0007t0004g0317 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.831+238G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27516051 | ||||||
chr8:27516191 | T | A | 1 | a0003c0006t0002g0358 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.832-129T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27516191 | ||||||
chr8:27516406 | T | C | 131 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(128): Show | 134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
splice_region_variant&intron_variant | LOW | c.910+8T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516406 | ||||||
chr8:27516410 | GTCTTGCA others(17): Show |
G | 1 | a0001c0002t0002g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.910+14_910+37delCT others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516410 | |||||
chr8:27516462 | C | T | 9 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(6): Show | 10 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.910+64C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516462 | ||||||
chr8:27516547 | C | T | 8 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(5): Show | 8 | HG02083.hp2 NA18939.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+149C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516547 | ||||||
chr8:27516663 | A | G | 1 | a0004c0010t0001g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.910+265A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516663 | ||||||
chr8:27516665 | A | G | 1 | a0001c0005t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.910+267A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516665 | ||||||
chr8:27516884 | C | T | 9 | a0001c0001t0001g0012a0004c0010t0001g0292a0004c0010t0001g0295others(6): Show | 10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.910+486C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516884 | ||||||
chr8:27516892 | T | G | 8 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0316others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+494T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516892 | ||||||
chr8:27516917 | C | CTT | 31 | a0001c0002t0002g0236a0001c0002t0002g0238a0001c0002t0002g0247others(28): Show | 32 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.910+520_910+521ins others(2): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516917 | |||||
chr8:27516917 | C | CTTT | 60 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(57): Show | 61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.910+520_910+521ins others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516917 | |||||
chr8:27516917 | C | CTTTT | 5 | a0001c0002t0002g0270a0001c0002t0002g0271a0001c0013t0002g0019others(2): Show | 5 | HG01515.hp1 HG01517.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+520_910+521ins others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516917 | |||||
chr8:27516919 | A | AT | 27 | a0001c0001t0001g0012a0001c0001t0001g0109a0001c0001t0001g0110others(24): Show | 29 | HG00639.hp2 HG01192.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.910+539dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516919 | |||||
chr8:27516919 | A | T | 96 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(93): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.910+521A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516919 | ||||||
chr8:27516919 | AT | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0112others(7): Show | 10 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.910+539delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516919 | |||||
chr8:27517063 | G | A | 1 | a0001c0005t0003g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.910+665G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517063 | ||||||
chr8:27517169 | A | T | 50 | a0001c0005t0003g0036a0002c0003t0002g0035a0002c0003t0002g0040others(47): Show | 54 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.910+771A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517169 | ||||||
chr8:27517200 | T | C | 1 | a0001c0001t0001g0006 | 2 | HG00738.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.910+802T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517200 | ||||||
chr8:27517282 | ACTACCCA others(3): Show |
A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.911-755_911-746del others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517282 | ||||||
chr8:27517315 | A | G | 2 | a0004c0015t0004g0288a0004c0015t0004g0289 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.911-723A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517315 | ||||||
chr8:27517381 | C | G | 3 | a0001c0004t0004g0327a0001c0004t0004g0328a0001c0004t0004g0329 | 3 | HG02258.hp2 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.911-657C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517381 | ||||||
chr8:27517409 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.911-629C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517409 | ||||||
chr8:27517418 | G | A | 9 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.911-620G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517418 | ||||||
chr8:27517636 | C | T | 3 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020 | 3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.911-402C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517636 | ||||||
chr8:27517795 | CAG | C | 8 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0316others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.911-242_911-241del others(2): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517795 | ||||||
chr8:27517886 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.911-152G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517886 | ||||||
chr8:27517928 | TTTG | T | 6 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(3): Show | 6 | HG02055.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.911-98_911-96delGT others(1): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27517928 | |||||
chr8:27518189 | A | T | 7 | a0003c0006t0002g0357a0003c0007t0004g0312a0003c0007t0004g0313others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+117A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518189 | ||||||
chr8:27518232 | C | T | 1 | a0003c0006t0002g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.945+160C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518232 | ||||||
chr8:27518323 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.945+251G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518323 | ||||||
chr8:27518343 | C | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.945+271C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518343 | ||||||
chr8:27518382 | C | T | 7 | a0003c0006t0002g0357a0003c0007t0004g0312a0003c0007t0004g0313others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+310C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518382 | ||||||
chr8:27518462 | T | C | 9 | a0001c0001t0001g0012a0004c0010t0001g0292a0004c0010t0001g0295others(6): Show | 10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.945+390T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518462 | ||||||
chr8:27518726 | T | C | 3 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020 | 3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.945+654T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518726 | ||||||
chr8:27518787 | T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0112 | 3 | NA18981.hp1 NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.945+715T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518787 | ||||||
chr8:27519002 | T | C | 2 | a0003c0007t0004g0312a0003c0007t0004g0313 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945+930T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519002 | ||||||
chr8:27519125 | A | G | 1 | a0001c0002t0002g0264 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.945+1053A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519125 | ||||||
chr8:27519133 | G | A | 1 | a0001c0013t0002g0019 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.945+1061G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519133 | ||||||
chr8:27519338 | C | T | 2 | a0003c0007t0004g0312a0003c0007t0004g0313 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945+1266C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519338 | ||||||
chr8:27519440 | C | T | 2 | a0001c0002t0002g0284a0001c0025t0001g0285 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.945+1368C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519440 | ||||||
chr8:27519631 | TG | T | 3 | a0001c0002t0002g0218a0001c0002t0002g0219a0001c0002t0002g0224 | 3 | HG02896.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.946-1251delG | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519631 | ||||||
chr8:27519645 | C | T | 63 | a0001c0001t0001g0179a0001c0002t0002g0010a0001c0002t0002g0017others(60): Show | 64 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.946-1238C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519645 | ||||||
chr8:27519646 | G | T | 1 | a0003c0006t0002g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.946-1237G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519646 | ||||||
chr8:27519716 | C | T | 1 | a0005c0009t0001g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.946-1167C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519716 | ||||||
chr8:27519772 | C | T | 1 | a0001c0002t0002g0257 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.946-1111C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519772 | ||||||
chr8:27519819 | A | C | 3 | a0003c0007t0004g0316a0003c0007t0004g0317a0003c0007t0004g0319 | 3 | HG02559.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.946-1064A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519819 | ||||||
chr8:27519837 | A | G | 1 | a0001c0004t0004g0328 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.946-1046A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519837 | ||||||
chr8:27519972 | G | A | 2 | a0004c0015t0004g0288a0004c0015t0004g0289 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.946-911G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519972 | ||||||
chr8:27520005 | T | C | 1 | a0001c0002t0002g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-878T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520005 | ||||||
chr8:27520006 | C | CT | 19 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(16): Show | 20 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.946-863dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 27520006 | |||||
chr8:27520006 | C | T | 1 | a0001c0002t0002g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-877C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520006 | ||||||
chr8:27520021 | A | G | 1 | a0003c0035t0001g0355 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.946-862A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520021 | ||||||
chr8:27520119 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.946-764G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520119 | ||||||
chr8:27520160 | T | A | 1 | a0001c0002t0002g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-723T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520160 | ||||||
chr8:27520162 | A | T | 1 | a0001c0002t0002g0237 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-721A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520162 | ||||||
chr8:27520228 | C | A | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.946-655C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520228 | ||||||
chr8:27520286 | C | T | 17 | a0001c0001t0001g0012a0003c0007t0004g0314a0003c0007t0004g0315others(14): Show | 18 | HG00639.hp2 HG01192.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.946-597C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520286 | ||||||
chr8:27520365 | T | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.946-518T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520365 | ||||||
chr8:27520427 | A | G | 1 | a0001c0002t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.946-456A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520427 | ||||||
chr8:27520440 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.946-443G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520440 | ||||||
chr8:27520492 | G | A | 2 | a0004c0015t0004g0288a0004c0015t0004g0289 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.946-391G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520492 | ||||||
chr8:27520584 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.946-299T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520584 | ||||||
chr8:27520592 | G | A | 1 | a0004c0010t0001g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.946-291G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520592 | ||||||
chr8:27520629 | G | T | 18 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(15): Show | 19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.946-254G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520629 | ||||||
chr8:27520640 | C | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.946-243C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520640 | ||||||
chr8:27520641 | G | A | 1 | a0001c0014t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.946-242G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520641 | ||||||
chr8:27520658 | T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0170 | 2 | HG02027.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.946-225T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520658 | ||||||
chr8:27520742 | T | A | 3 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020 | 3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.946-141T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520742 | ||||||
chr8:27520878 | C | T | 5 | a0003c0007t0004g0316a0003c0007t0004g0317a0003c0007t0004g0319others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.946-5C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520878 | ||||||
chr8:27520986 | C | T | 9 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.972+77C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27520986 | ||||||
chr8:27521000 | C | T | 2 | a0004c0010t0001g0297a0004c0010t0001g0298 | 2 | HG00639.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.972+91C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521000 | ||||||
chr8:27521032 | G | C | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.972+123G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521032 | ||||||
chr8:27521087 | T | G | 4 | a0001c0005t0003g0082a0001c0005t0003g0083a0001c0005t0003g0084others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+178T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521087 | ||||||
chr8:27521101 | G | T | 1 | a0001c0002t0002g0257 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.972+192G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521101 | ||||||
chr8:27521116 | T | C | 151 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(148): Show | 154 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.972+207T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521116 | ||||||
chr8:27521213 | G | A | 1 | a0003c0007t0004g0312 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.972+304G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521213 | ||||||
chr8:27521400 | G | A | 20 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(17): Show | 21 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.972+491G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521400 | ||||||
chr8:27521515 | C | T | 1 | a0001c0005t0005g0230 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.972+606C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521515 | ||||||
chr8:27521606 | C | A | 1 | a0002c0003t0003g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.972+697C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521606 | ||||||
chr8:27521797 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.973-626G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521797 | ||||||
chr8:27521804 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.973-619G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521804 | ||||||
chr8:27521812 | C | T | 6 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(3): Show | 7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-611C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521812 | ||||||
chr8:27521813 | G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0137 | 3 | HG01257.hp2 HG01361.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.973-610G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521813 | ||||||
chr8:27521949 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.973-474G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521949 | ||||||
chr8:27521972 | C | T | 1 | a0001c0002t0002g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.973-451C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521972 | ||||||
chr8:27522082 | G | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.973-341G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27522082 | ||||||
chr8:27522140 | A | AAGG | 280 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0021others(277): Show | 288 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.973-281_973-280ins others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 27522140 | |||||
chr8:27522303 | G | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0165others(1): Show | 4 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-120G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27522303 | ||||||
chr8:27522304 | A | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0165others(1): Show | 4 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-119A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27522304 | ||||||
chr8:27522646 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1058+138A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522646 | ||||||
chr8:27522681 | G | A | 1 | a0002c0003t0003g0038 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1058+173G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522681 | ||||||
chr8:27522750 | A | G | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058+242A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522750 | ||||||
chr8:27522845 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1058+337C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522845 | ||||||
chr8:27522876 | G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0173others(1): Show | 4 | HG01109.hp2 HG02602.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+368G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522876 | ||||||
chr8:27522942 | C | T | 4 | a0001c0002t0002g0231a0001c0002t0002g0232a0001c0002t0002g0233others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+434C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522942 | ||||||
chr8:27522962 | C | CA | 27 | a0001c0001t0001g0021a0001c0001t0001g0090a0001c0001t0001g0092others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1058+479dupA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | |||||
chr8:27522962 | CA | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0130others(26): Show | 30 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1058+479delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | |||||
chr8:27522962 | CAA | C | 91 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(88): Show | 93 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1058+478_1058+479d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | |||||
chr8:27522962 | CAAA | C | 15 | a0001c0001t0001g0012a0001c0002t0002g0245a0001c0002t0002g0271others(12): Show | 16 | HG00639.hp2 HG01192.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1058+477_1058+479d others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | |||||
chr8:27523036 | G | T | 6 | a0001c0002t0002g0246a0001c0002t0002g0250a0001c0002t0002g0253others(3): Show | 6 | NA18949.hp2 NA18956.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+528G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523036 | ||||||
chr8:27523078 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1058+570A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523078 | ||||||
chr8:27523246 | G | A | 5 | a0007c0012t0001g0299a0007c0012t0001g0301a0007c0012t0001g0302others(2): Show | 5 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+738G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523246 | ||||||
chr8:27523414 | C | T | 2 | a0003c0007t0004g0315a0003c0007t0004g0321 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1058+906C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523414 | ||||||
chr8:27523650 | T | C | 10 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1058+1142T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523650 | ||||||
chr8:27523677 | G | C | 141 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(138): Show | 144 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.1058+1169G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523677 | ||||||
chr8:27523690 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1058+1182C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523690 | ||||||
chr8:27523715 | T | A | 9 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1058+1207T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523715 | ||||||
chr8:27523762 | C | G | 4 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(1): Show | 5 | HG02145.hp1 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+1254C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523762 | ||||||
chr8:27523874 | C | T | 2 | a0009c0018t0001g0300a0009c0018t0001g0303 | 2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1058+1366C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523874 | ||||||
chr8:27523935 | GT | G | 124 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(121): Show | 126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1059-1412delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27523935 | |||||
chr8:27523935 | GTT | G | 10 | a0001c0001t0001g0012a0003c0006t0002g0357a0004c0010t0001g0292others(7): Show | 11 | HG00639.hp2 HG01192.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1059-1413_1059-141 others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27523935 | |||||
chr8:27523955 | CAG | C | 3 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0321 | 3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1059-1404_1059-140 others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27523955 | |||||
chr8:27524125 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1059-1237G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524125 | ||||||
chr8:27524241 | TATTCCTT others(8): Show |
T | 72 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059-1118_1059-110 others(19): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27524241 | |||||
chr8:27524379 | G | C | 2 | a0002c0011t0001g0222a0002c0011t0001g0223 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1059-983G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524379 | ||||||
chr8:27524479 | C | G | 70 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(67): Show | 71 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1059-883C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524479 | ||||||
chr8:27524683 | C | G | 6 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(3): Show | 7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-679C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524683 | ||||||
chr8:27524896 | T | C | 1 | a0003c0006t0002g0361 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059-466T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524896 | ||||||
chr8:27524987 | GA | G | 150 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(147): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1059-367delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27524987 | |||||
chr8:27525068 | C | CTG | 34 | a0001c0001t0001g0024a0001c0001t0001g0097a0001c0001t0001g0103others(31): Show | 37 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1059-255_1059-254d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | C | CTGTG | 21 | a0001c0001t0001g0098a0001c0001t0001g0119a0001c0001t0001g0129others(18): Show | 22 | HG00140.hp1 HG01255.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059-257_1059-254d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | C | CTGTGTG | 3 | a0001c0001t0001g0118a0001c0005t0002g0229a0002c0003t0003g0058 | 3 | HG02004.hp2 HG03195.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1059-259_1059-254d others(8): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | CTG | C | 92 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0025others(89): Show | 94 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1059-255_1059-254d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | CTGTG | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0109a0001c0005t0002g0078others(9): Show | 12 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1059-257_1059-254d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | CTGTGTG | C | 4 | a0001c0001t0001g0101a0001c0005t0003g0082a0001c0005t0003g0085others(1): Show | 4 | HG02630.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059-259_1059-254d others(8): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | CTGTGTGT others(1): Show |
C | 7 | a0001c0002t0002g0277a0003c0007t0004g0316a0003c0007t0004g0317others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059-261_1059-254d others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | CTGTGTGT others(5): Show |
C | 3 | a0001c0002t0002g0218a0001c0002t0002g0219a0001c0002t0002g0224 | 3 | HG02896.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1059-265_1059-254d others(14): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525068 | CTGTGTGT others(9): Show |
C | 3 | a0001c0001t0001g0171a0001c0001t0001g0186a0014c0027t0001g0161 | 3 | HG00323.hp2 HG01515.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1059-269_1059-254d others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | |||||
chr8:27525093 | TGTGTGTG others(19): Show |
T | 3 | a0001c0002t0002g0251a0001c0002t0002g0252a0001c0002t0002g0268 | 3 | NA19012.hp1 NA19077.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1059-267_1059-242d others(28): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525093 | |||||
chr8:27525095 | TGTGTGTG others(7): Show |
T | 10 | a0001c0002t0002g0257a0001c0004t0003g0331a0001c0004t0003g0333others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-265_1059-252d others(16): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525095 | |||||
chr8:27525095 | TGTGTGTG others(11): Show |
T | 1 | a0001c0013t0006g0020 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1059-265_1059-248d others(20): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525095 | |||||
chr8:27525095 | TGTGTGTG others(13): Show |
T | 6 | a0001c0002t0002g0246a0001c0002t0002g0250a0001c0002t0002g0253others(3): Show | 6 | NA18949.hp2 NA18956.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059-265_1059-246d others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525095 | |||||
chr8:27525097 | T | C | 5 | a0001c0002t0002g0243a0001c0002t0002g0265a0001c0002t0002g0270others(2): Show | 5 | HG01515.hp1 HG01517.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059-265T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525097 | ||||||
chr8:27525099 | T | C | 10 | a0001c0002t0002g0243a0001c0002t0002g0262a0001c0002t0002g0265others(7): Show | 10 | HG01515.hp1 HG01517.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-263T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525099 | ||||||
chr8:27525099 | T | TGC | 24 | a0001c0002t0002g0010a0001c0002t0002g0236a0001c0002t0002g0238others(21): Show | 25 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1059-262_1059-261i others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525099 | |||||
chr8:27525099 | T | TGCGC | 4 | a0001c0002t0002g0242a0001c0002t0002g0244a0001c0002t0002g0245others(1): Show | 4 | HG02698.hp1 NA18941.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-262_1059-261i others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525099 | |||||
chr8:27525099 | TGTGTGTG others(3): Show |
T | 2 | a0001c0002t0002g0266a0001c0002t0002g0275 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1059-261_1059-252d others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525099 | |||||
chr8:27525101 | T | C | 52 | a0001c0002t0002g0010a0001c0002t0002g0231a0001c0002t0002g0232others(49): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1059-261T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525101 | ||||||
chr8:27525101 | T | TGCGC | 4 | a0001c0002t0002g0237a0001c0002t0002g0260a0001c0004t0004g0336others(1): Show | 4 | HG00621.hp1 HG03130.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-260_1059-259i others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525101 | |||||
chr8:27525103 | T | C | 60 | a0001c0002t0002g0010a0001c0002t0002g0231a0001c0002t0002g0232others(57): Show | 61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1059-259T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525103 | ||||||
chr8:27525103 | T | TGCGCGC | 4 | a0001c0002t0002g0280a0001c0002t0002g0282a0001c0004t0004g0337others(1): Show | 4 | HG00609.hp2 HG03098.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-258_1059-257i others(8): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525103 | |||||
chr8:27525105 | T | A | 1 | a0001c0002t0002g0262 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1059-257T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525105 | ||||||
chr8:27525105 | T | C | 76 | a0001c0001t0001g0021a0001c0002t0002g0010a0001c0002t0002g0018others(73): Show | 77 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1059-257T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525105 | ||||||
chr8:27525105 | T | TGCGCGCG others(3): Show |
1 | a0001c0002t0002g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1059-256_1059-255i others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525105 | |||||
chr8:27525107 | T | C | 106 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0094others(103): Show | 109 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1059-255T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525107 | ||||||
chr8:27525107 | T | TGC | 10 | a0001c0001t0001g0013a0001c0001t0001g0110a0001c0001t0001g0155others(7): Show | 10 | HG02602.hp1 HG03139.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-240_1059-239d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | |||||
chr8:27525107 | T | TGCGC | 3 | a0001c0001t0001g0125a0001c0004t0004g0329a0002c0003t0003g0063 | 3 | HG00544.hp1 HG02486.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1059-242_1059-239d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | |||||
chr8:27525107 | T | TGTGC | 7 | a0001c0004t0004g0327a0001c0004t0004g0328a0001c0014t0003g0346others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059-254_1059-253i others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | |||||
chr8:27525107 | T | TGTGCGCG others(5): Show |
2 | a0001c0004t0004g0338a0001c0004t0004g0339 | 2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1059-254_1059-253i others(14): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | |||||
chr8:27525107 | T | TGTGCGCG others(11): Show |
1 | a0001c0013t0002g0019 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1059-254_1059-253i others(20): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | |||||
chr8:27525107 | T | TGTGTGCG others(9): Show |
1 | a0001c0002t0002g0240 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1059-254_1059-253i others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | |||||
chr8:27525107 | T | TGTGTGTG others(1): Show |
3 | a0001c0014t0003g0345a0002c0003t0003g0032a0002c0003t0003g0217 | 3 | HG01192.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1059-254_1059-253i others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | |||||
chr8:27525109 | C | T | 5 | a0001c0001t0001g0304a0001c0013t0002g0273a0003c0007t0004g0312others(2): Show | 5 | HG00733.hp1 HG00738.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059-253C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525109 | ||||||
chr8:27525111 | C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG00558.hp1 HG02027.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-251C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525111 | ||||||
chr8:27525114 | G | A | 1 | a0001c0014t0003g0345 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1059-248G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525114 | ||||||
chr8:27525116 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1059-246G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525116 | ||||||
chr8:27525498 | A | G | 1 | a0001c0005t0006g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1170+25A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525498 | ||||||
chr8:27525706 | T | A | 10 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+233T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525706 | ||||||
chr8:27525712 | G | GA | 10 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+240dupA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27525712 | |||||
chr8:27525845 | A | G | 1 | a0003c0006t0002g0353 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1170+372A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525845 | ||||||
chr8:27525913 | G | T | 2 | a0002c0011t0001g0222a0002c0011t0001g0223 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1170+440G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525913 | ||||||
chr8:27525999 | C | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1170+526C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525999 | ||||||
chr8:27526019 | C | T | 1 | a0004c0010t0001g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1170+546C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526019 | ||||||
chr8:27526187 | C | T | 7 | a0003c0006t0002g0357a0003c0007t0004g0312a0003c0007t0004g0313others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+714C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526187 | ||||||
chr8:27526250 | C | T | 7 | a0003c0006t0002g0357a0003c0007t0004g0312a0003c0007t0004g0313others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+777C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526250 | ||||||
chr8:27526384 | G | T | 72 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1170+911G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526384 | ||||||
chr8:27526896 | G | T | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1170+1423G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526896 | ||||||
chr8:27526989 | G | A | 35 | a0001c0001t0001g0012a0001c0004t0003g0331a0001c0004t0003g0333others(32): Show | 36 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1170+1516G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526989 | ||||||
chr8:27527002 | G | T | 1 | a0001c0002t0002g0248 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1170+1529G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527002 | ||||||
chr8:27527315 | C | T | 8 | a0001c0002t0002g0235a0001c0002t0002g0236a0001c0002t0002g0237others(5): Show | 8 | HG02723.hp1 HG02970.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+1842C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527315 | ||||||
chr8:27527359 | T | C | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+1886T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527359 | ||||||
chr8:27527414 | T | C | 7 | a0003c0006t0002g0357a0003c0007t0004g0312a0003c0007t0004g0313others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+1941T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527414 | ||||||
chr8:27527760 | G | A | 1 | a0003c0007t0004g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1170+2287G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527760 | ||||||
chr8:27527898 | C | T | 148 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(145): Show | 151 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1170+2425C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527898 | ||||||
chr8:27527933 | A | G | 113 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(110): Show | 115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1170+2460A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527933 | ||||||
chr8:27527948 | G | A | 9 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(6): Show | 10 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+2475G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527948 | ||||||
chr8:27528035 | G | A | 2 | a0003c0006t0002g0351a0003c0006t0002g0352 | 2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1170+2562G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528035 | ||||||
chr8:27528185 | T | C | 1 | a0003c0006t0002g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1170+2712T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528185 | ||||||
chr8:27528349 | T | A | 17 | a0001c0001t0001g0012a0003c0007t0004g0314a0003c0007t0004g0315others(14): Show | 18 | HG00639.hp2 HG01192.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1170+2876T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528349 | ||||||
chr8:27528400 | G | T | 7 | a0003c0006t0002g0357a0003c0007t0004g0312a0003c0007t0004g0313others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+2927G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528400 | ||||||
chr8:27528449 | C | T | 1 | a0001c0002t0002g0248 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1170+2976C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528449 | ||||||
chr8:27528516 | T | C | 1 | a0002c0003t0003g0055 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1170+3043T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528516 | ||||||
chr8:27528522 | T | G | 2 | a0002c0008t0002g0042a0002c0008t0002g0048 | 2 | NA18955.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1170+3049T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528522 | ||||||
chr8:27528523 | G | T | 9 | a0001c0001t0001g0012a0004c0010t0001g0292a0004c0010t0001g0295others(6): Show | 10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+3050G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528523 | ||||||
chr8:27528592 | A | G | 2 | a0002c0003t0003g0027a0002c0003t0003g0028 | 2 | NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1170+3119A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528592 | ||||||
chr8:27528736 | T | A | 1 | a0005c0009t0001g0164 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1170+3263T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528736 | ||||||
chr8:27528878 | C | T | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1170+3405C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528878 | ||||||
chr8:27528920 | C | T | 3 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0321 | 3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1170+3447C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528920 | ||||||
chr8:27528921 | G | A | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+3448G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528921 | ||||||
chr8:27529078 | G | A | 9 | a0001c0001t0001g0012a0004c0010t0001g0292a0004c0010t0001g0295others(6): Show | 10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+3605G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529078 | ||||||
chr8:27529115 | C | T | 1 | a0002c0003t0003g0055 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1170+3642C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529115 | ||||||
chr8:27529253 | T | C | 2 | a0011c0033t0004g0015a0019c0037t0004g0016 | 2 | HG00738.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1170+3780T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529253 | ||||||
chr8:27529408 | ACTTGGCC others(6): Show |
A | 1 | a0018c0022t0002g0283 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1170+3936_1170+394 others(17): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529408 | ||||||
chr8:27529457 | G | T | 26 | a0001c0001t0001g0012a0001c0004t0003g0331a0001c0004t0003g0333others(23): Show | 27 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1170+3984G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529457 | ||||||
chr8:27529498 | C | T | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+4025C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529498 | ||||||
chr8:27529499 | G | A | 1 | a0003c0007t0004g0320 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1170+4026G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529499 | ||||||
chr8:27529653 | G | A | 1 | a0001c0002t0002g0284 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1170+4180G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529653 | ||||||
chr8:27529713 | C | G | 150 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(147): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+4240C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529713 | ||||||
chr8:27529791 | A | G | 74 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(71): Show | 75 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1170+4318A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529791 | ||||||
chr8:27529875 | C | T | 116 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(113): Show | 118 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1170+4402C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529875 | ||||||
chr8:27529885 | T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0188 | 2 | NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1170+4412T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529885 | ||||||
chr8:27529888 | GC | G | 4 | a0007c0012t0001g0301a0007c0012t0001g0302a0009c0018t0001g0300others(1): Show | 4 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+4416delC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529888 | ||||||
chr8:27529889 | CA | C | 150 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(147): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+4430delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27529889 | |||||
chr8:27530067 | CT | C | 150 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(147): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+4607delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530067 | |||||
chr8:27530075 | T | C | 1 | a0003c0006t0002g0357 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1170+4602T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530075 | ||||||
chr8:27530117 | G | A | 9 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+4644G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530117 | ||||||
chr8:27530192 | G | A | 1 | a0001c0002t0002g0234 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1170+4719G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530192 | ||||||
chr8:27530227 | C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0180a0001c0001t0001g0192others(1): Show | 4 | HG01891.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4754C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530227 | ||||||
chr8:27530250 | G | A | 6 | a0003c0007t0004g0312a0003c0007t0004g0313a0004c0015t0004g0288others(3): Show | 6 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+4777G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530250 | ||||||
chr8:27530269 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1170+4796A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530269 | ||||||
chr8:27530328 | A | C | 24 | a0001c0005t0003g0036a0002c0003t0002g0035a0002c0003t0002g0040others(21): Show | 28 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1170+4855A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530328 | ||||||
chr8:27530331 | G | T | 6 | a0003c0007t0004g0312a0003c0007t0004g0313a0004c0015t0004g0288others(3): Show | 6 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+4858G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530331 | ||||||
chr8:27530355 | G | A | 21 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(18): Show | 21 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1170+4882G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530355 | ||||||
chr8:27530446 | A | G | 1 | a0002c0003t0003g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1170+4973A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530446 | ||||||
chr8:27530642 | C | A | 2 | a0001c0014t0003g0346a0001c0014t0003g0347 | 2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1170+5169C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530642 | ||||||
chr8:27530659 | T | TATTTTGA others(15): Show |
1 | a0001c0002t0002g0278 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1170+5187_1170+520 others(26): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530659 | |||||
chr8:27530682 | G | A | 124 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(121): Show | 126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1170+5209G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530682 | ||||||
chr8:27530762 | CT | C | 111 | a0001c0001t0001g0226a0001c0001t0001g0249a0001c0002t0002g0010others(108): Show | 112 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1170+5307delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530762 | |||||
chr8:27530762 | CTT | C | 16 | a0001c0001t0001g0012a0001c0002t0002g0231a0001c0002t0002g0232others(13): Show | 17 | HG00639.hp2 HG01192.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1170+5306_1170+530 others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530762 | |||||
chr8:27530803 | C | G | 150 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(147): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+5330C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530803 | ||||||
chr8:27530828 | A | T | 124 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(121): Show | 126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1170+5355A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530828 | ||||||
chr8:27530891 | G | A | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+5418G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530891 | ||||||
chr8:27530965 | G | A | 1 | a0005c0009t0001g0164 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1170+5492G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530965 | ||||||
chr8:27531015 | G | A | 9 | a0002c0008t0002g0053a0003c0007t0004g0314a0003c0007t0004g0315others(6): Show | 9 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+5542G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531015 | ||||||
chr8:27531059 | G | T | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1170+5586G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531059 | ||||||
chr8:27531276 | C | T | 1 | a0002c0008t0002g0044 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1171-5508C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531276 | ||||||
chr8:27531435 | G | A | 10 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-5349G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531435 | ||||||
chr8:27531538 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1171-5246A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531538 | ||||||
chr8:27531570 | C | T | 1 | a0003c0006t0002g0357 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1171-5214C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531570 | ||||||
chr8:27531575 | C | T | 1 | a0001c0002t0002g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1171-5209C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531575 | ||||||
chr8:27531604 | T | C | 12 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-5180T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531604 | ||||||
chr8:27531650 | G | A | 32 | a0001c0001t0001g0012a0001c0004t0003g0331a0001c0004t0003g0333others(29): Show | 33 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1171-5134G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531650 | ||||||
chr8:27531688 | G | A | 2 | a0001c0002t0002g0270a0001c0002t0002g0271 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1171-5096G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531688 | ||||||
chr8:27531710 | A | G | 1 | a0001c0005t0003g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1171-5074A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531710 | ||||||
chr8:27531743 | T | C | 2 | a0011c0033t0004g0015a0019c0037t0004g0016 | 2 | HG00738.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1171-5041T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531743 | ||||||
chr8:27531782 | C | T | 12 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(9): Show | 13 | HG01243.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1171-5002C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531782 | ||||||
chr8:27531917 | C | G | 2 | a0003c0007t0004g0317a0003c0007t0004g0319 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1171-4867C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531917 | ||||||
chr8:27531918 | A | G | 1 | a0001c0005t0003g0036 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1171-4866A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531918 | ||||||
chr8:27531939 | C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0114a0001c0001t0001g0116others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1171-4845C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531939 | ||||||
chr8:27531940 | G | A | 148 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(145): Show | 151 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1171-4844G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531940 | ||||||
chr8:27531941 | C | A | 1 | a0001c0002t0002g0278 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1171-4843C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531941 | ||||||
chr8:27532006 | G | A | 73 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(70): Show | 74 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1171-4778G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532006 | ||||||
chr8:27532021 | A | G | 1 | a0001c0002t0002g0276 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1171-4763A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532021 | ||||||
chr8:27532025 | T | C | 151 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(148): Show | 154 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1171-4759T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532025 | ||||||
chr8:27532101 | A | T | 9 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1171-4683A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532101 | ||||||
chr8:27532114 | G | A | 12 | a0001c0001t0001g0076a0001c0001t0001g0176a0001c0001t0001g0177others(9): Show | 13 | HG00323.hp1 HG00733.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1171-4670G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532114 | ||||||
chr8:27532185 | C | T | 12 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(9): Show | 12 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-4599C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532185 | ||||||
chr8:27532258 | G | A | 1 | a0001c0014t0003g0346 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1171-4526G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532258 | ||||||
chr8:27532511 | G | A | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1171-4273G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532511 | ||||||
chr8:27532552 | T | C | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1171-4232T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532552 | ||||||
chr8:27532615 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1171-4169G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532615 | ||||||
chr8:27532675 | G | A | 154 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(151): Show | 157 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1171-4109G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532675 | ||||||
chr8:27532729 | T | G | 72 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1171-4055T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532729 | ||||||
chr8:27532799 | C | T | 1 | a0001c0005t0002g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1171-3985C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532799 | ||||||
chr8:27532858 | A | G | 10 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-3926A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532858 | ||||||
chr8:27532977 | T | G | 3 | a0003c0006t0002g0350a0003c0006t0002g0360a0003c0006t0002g0361 | 3 | HG02293.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1171-3807T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532977 | ||||||
chr8:27533080 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1171-3704A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533080 | ||||||
chr8:27533101 | C | A | 2 | a0002c0003t0003g0055a0002c0003t0003g0064 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1171-3683C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533101 | ||||||
chr8:27533203 | A | G | 1 | a0003c0007t0008g0306 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1171-3581A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533203 | ||||||
chr8:27533293 | C | G | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1171-3491C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533293 | ||||||
chr8:27533423 | A | G | 1 | a0020c0036t0002g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1171-3361A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533423 | ||||||
chr8:27533438 | G | A | 9 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(6): Show | 10 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-3346G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533438 | ||||||
chr8:27533603 | TA | T | 6 | a0001c0001t0001g0200a0001c0001t0001g0204a0001c0001t0001g0209others(3): Show | 6 | HG00423.hp1 NA18951.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-3179delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27533603 | |||||
chr8:27533674 | A | C | 118 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(115): Show | 120 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1171-3110A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533674 | ||||||
chr8:27533842 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1171-2942C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533842 | ||||||
chr8:27533843 | C | A | 11 | a0001c0001t0001g0012a0002c0011t0001g0222a0002c0011t0001g0223others(8): Show | 12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-2941C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533843 | ||||||
chr8:27533848 | G | A | 72 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1171-2936G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533848 | ||||||
chr8:27533919 | C | T | 12 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-2865C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533919 | ||||||
chr8:27534063 | G | A | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1171-2721G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534063 | ||||||
chr8:27534103 | G | C | 153 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(150): Show | 156 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1171-2681G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534103 | ||||||
chr8:27534139 | T | C | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1171-2645T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534139 | ||||||
chr8:27534143 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1171-2641G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534143 | ||||||
chr8:27534272 | C | T | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-2512C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534272 | ||||||
chr8:27534286 | T | C | 3 | a0002c0003t0003g0026a0002c0003t0003g0027a0002c0003t0003g0028 | 3 | NA18952.hp1 NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1171-2498T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534286 | ||||||
chr8:27534288 | T | A | 5 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020others(2): Show | 5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1171-2496T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534288 | ||||||
chr8:27534323 | G | A | 2 | a0002c0008t0002g0042a0002c0008t0002g0048 | 2 | NA18955.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1171-2461G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534323 | ||||||
chr8:27534407 | T | C | 12 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-2377T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534407 | ||||||
chr8:27534408 | T | C | 9 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1171-2376T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534408 | ||||||
chr8:27534424 | G | A | 1 | a0003c0007t0004g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1171-2360G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534424 | ||||||
chr8:27534601 | G | A | 1 | a0003c0007t0004g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1171-2183G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534601 | ||||||
chr8:27534645 | AAAAAAT | A | 11 | a0001c0001t0001g0012a0002c0011t0001g0222a0002c0011t0001g0223others(8): Show | 12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-2127_1171-212 others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27534645 | |||||
chr8:27534705 | G | A | 1 | a0002c0003t0003g0066 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1171-2079G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534705 | ||||||
chr8:27534740 | T | A | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-2044T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534740 | ||||||
chr8:27534873 | C | T | 1 | a0002c0008t0002g0041 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1171-1911C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534873 | ||||||
chr8:27534878 | T | C | 72 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1171-1906T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534878 | ||||||
chr8:27534922 | C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092 | 3 | HG00558.hp1 HG02080.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1171-1862C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534922 | ||||||
chr8:27535026 | C | G | 12 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-1758C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535026 | ||||||
chr8:27535158 | C | T | 2 | a0003c0007t0004g0312a0003c0007t0004g0313 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1171-1626C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535158 | ||||||
chr8:27535163 | A | ATATTT | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-1600_1171-159 others(9): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27535163 | |||||
chr8:27535163 | ATATTTTA others(8): Show |
A | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1171-1610_1171-159 others(19): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27535163 | |||||
chr8:27535427 | G | A | 3 | a0003c0006t0002g0350a0003c0006t0002g0360a0003c0006t0002g0361 | 3 | HG02293.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1171-1357G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535427 | ||||||
chr8:27535469 | C | T | 124 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(121): Show | 126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1171-1315C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535469 | ||||||
chr8:27535470 | G | T | 1 | a0001c0002t0002g0278 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1171-1314G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535470 | ||||||
chr8:27535536 | T | C | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1171-1248T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535536 | ||||||
chr8:27535549 | G | A | 118 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(115): Show | 120 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1171-1235G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535549 | ||||||
chr8:27535593 | C | T | 1 | a0001c0002t0002g0234 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1171-1191C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535593 | ||||||
chr8:27535634 | C | A | 1 | a0003c0035t0001g0355 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1171-1150C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535634 | ||||||
chr8:27535703 | T | G | 150 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(147): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1171-1081T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535703 | ||||||
chr8:27535939 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1171-845T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535939 | ||||||
chr8:27536015 | C | T | 6 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(3): Show | 7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1171-769C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536015 | ||||||
chr8:27536063 | G | C | 1 | a0002c0003t0003g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1171-721G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536063 | ||||||
chr8:27536186 | A | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0206 | 2 | NA18939.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1171-598A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536186 | ||||||
chr8:27536205 | G | A | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-579G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536205 | ||||||
chr8:27536347 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1171-437G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536347 | ||||||
chr8:27536436 | C | T | 12 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-348C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536436 | ||||||
chr8:27536501 | A | G | 11 | a0001c0001t0001g0012a0002c0011t0001g0222a0002c0011t0001g0223others(8): Show | 12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-283A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536501 | ||||||
chr8:27536542 | A | G | 1 | a0002c0003t0003g0046 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1171-242A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536542 | ||||||
chr8:27536547 | G | C | 2 | a0003c0007t0008g0306a0003c0007t0008g0307 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1171-237G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536547 | ||||||
chr8:27536575 | G | A | 1 | a0003c0006t0002g0357 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1171-209G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536575 | ||||||
chr8:27536582 | A | G | 12 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-202A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536582 | ||||||
chr8:27536740 | C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0114a0001c0001t0001g0116others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1171-44C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536740 | ||||||
chr8:27536870 | T | C | 32 | a0001c0001t0001g0012a0001c0004t0003g0331a0001c0004t0003g0333others(29): Show | 33 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1242+15T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27536870 | ||||||
chr8:27536917 | C | A | 1 | a0016c0026t0002g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1242+62C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27536917 | ||||||
chr8:27536999 | C | G | 5 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020others(2): Show | 5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+144C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27536999 | ||||||
chr8:27537022 | G | A | 13 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(10): Show | 13 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1242+167G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537022 | ||||||
chr8:27537207 | G | C | 152 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(149): Show | 155 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1242+352G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537207 | ||||||
chr8:27537210 | G | A | 11 | a0001c0001t0001g0012a0002c0011t0001g0222a0002c0011t0001g0223others(8): Show | 12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1242+355G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537210 | ||||||
chr8:27537354 | C | T | 5 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020others(2): Show | 5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+499C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537354 | ||||||
chr8:27537440 | C | A | 120 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(117): Show | 122 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1242+585C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537440 | ||||||
chr8:27537465 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1242+610G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537465 | ||||||
chr8:27537485 | T | C | 5 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020others(2): Show | 5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+630T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537485 | ||||||
chr8:27537581 | A | G | 2 | a0002c0003t0003g0022a0002c0003t0003g0023 | 2 | HG00140.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1242+726A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537581 | ||||||
chr8:27537691 | T | A | 1 | a0001c0002t0002g0242 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1242+836T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537691 | ||||||
chr8:27537732 | T | C | 120 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(117): Show | 122 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1242+877T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537732 | ||||||
chr8:27537751 | A | G | 5 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020others(2): Show | 5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+896A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537751 | ||||||
chr8:27537937 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1243-722A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537937 | ||||||
chr8:27537943 | C | T | 9 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1243-716C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537943 | ||||||
chr8:27537999 | G | A | 2 | a0004c0015t0004g0288a0004c0015t0004g0289 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1243-660G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537999 | ||||||
chr8:27538147 | G | T | 12 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(9): Show | 13 | HG01243.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1243-512G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538147 | ||||||
chr8:27538394 | C | T | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1243-265C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538394 | ||||||
chr8:27538472 | C | T | 2 | a0001c0002t0002g0258a0001c0002t0002g0263 | 2 | HG00438.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1243-187C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538472 | ||||||
chr8:27538594 | G | T | 120 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(117): Show | 122 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1243-65G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538594 | ||||||
chr8:27538599 | G | A | 8 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0316others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-60G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538599 | ||||||
chr8:27538746 | A | G | 1 | a0014c0027t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1276+54A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538746 | ||||||
chr8:27538827 | C | T | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+135C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538827 | ||||||
chr8:27538852 | C | G | 3 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0321 | 3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1276+160C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538852 | ||||||
chr8:27538858 | C | G | 1 | a0003c0006t0002g0357 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1276+166C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538858 | ||||||
chr8:27538935 | G | C | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+243G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538935 | ||||||
chr8:27539006 | T | C | 152 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(149): Show | 155 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1276+314T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539006 | ||||||
chr8:27539030 | T | C | 32 | a0001c0001t0001g0012a0001c0004t0003g0331a0001c0004t0003g0333others(29): Show | 33 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1276+338T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539030 | ||||||
chr8:27539096 | C | T | 12 | a0001c0004t0004g0336a0001c0004t0004g0337a0001c0004t0004g0338others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1276+404C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539096 | ||||||
chr8:27539350 | C | T | 3 | a0001c0014t0003g0345a0001c0014t0003g0346a0001c0014t0003g0347 | 3 | HG01243.hp2 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1276+658C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539350 | ||||||
chr8:27539384 | C | G | 2 | a0004c0010t0007g0293a0004c0010t0007g0294 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1276+692C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539384 | ||||||
chr8:27539511 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1276+819C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539511 | ||||||
chr8:27539528 | T | C | 362 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(359): Show | 373 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.1276+836T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539528 | ||||||
chr8:27539570 | C | T | 41 | a0001c0005t0003g0144a0001c0005t0003g0168a0002c0003t0003g0001others(38): Show | 45 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1276+878C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539570 | ||||||
chr8:27539640 | T | C | 152 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(149): Show | 155 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1277-914T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539640 | ||||||
chr8:27539652 | C | G | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-902C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539652 | ||||||
chr8:27539709 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1277-845C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539709 | ||||||
chr8:27539734 | C | T | 8 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1277-820C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539734 | ||||||
chr8:27539846 | C | T | 11 | a0003c0006t0002g0310a0003c0006t0002g0311a0003c0006t0002g0350others(8): Show | 11 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1277-708C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539846 | ||||||
chr8:27539852 | C | G | 17 | a0001c0002t0002g0231a0001c0002t0002g0232a0001c0002t0002g0233others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1277-702C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539852 | ||||||
chr8:27539881 | G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0100 | 2 | HG02083.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1277-673G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539881 | ||||||
chr8:27539902 | C | T | 3 | a0003c0007t0008g0306a0003c0007t0008g0307a0003c0007t0012g0318 | 3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1277-652C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539902 | ||||||
chr8:27539976 | G | T | 3 | a0003c0007t0008g0306a0003c0007t0008g0307a0003c0007t0012g0318 | 3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1277-578G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539976 | ||||||
chr8:27539982 | A | G | 1 | a0002c0003t0003g0049 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1277-572A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539982 | ||||||
chr8:27540069 | G | T | 2 | a0004c0015t0004g0288a0004c0015t0004g0289 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1277-485G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540069 | ||||||
chr8:27540153 | C | T | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-401C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540153 | ||||||
chr8:27540166 | C | T | 10 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(7): Show | 10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1277-388C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540166 | ||||||
chr8:27540213 | C | T | 2 | a0003c0007t0004g0312a0003c0007t0004g0313 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1277-341C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540213 | ||||||
chr8:27540317 | C | T | 15 | a0001c0004t0004g0327a0001c0004t0004g0328a0001c0004t0004g0329others(12): Show | 15 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1277-237C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540317 | ||||||
chr8:27540364 | C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0110 | 3 | NA18989.hp1 NA19000.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1277-190C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540364 | ||||||
chr8:27540369 | G | A | 7 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0316others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-185G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540369 | ||||||
chr8:27540373 | A | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(11): Show | 14 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1277-181A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540373 | ||||||
chr8:27540454 | C | T | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-100C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540454 | ||||||
chr8:27540552 | A | G | 1 | a0001c0004t0004g0327 | 1 | NA19240.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1277-2A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540552 | ||||||
chr8:27540915 | T | C | 203 | a0001c0001t0001g0012a0001c0001t0001g0157a0001c0002t0002g0010others(200): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1379+259T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27540915 | ||||||
chr8:27541103 | C | T | 57 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(54): Show | 62 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1380-370C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27541103 | ||||||
chr8:27541159 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1380-314C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27541159 | ||||||
chr8:27541296 | G | A | 35 | a0001c0001t0001g0012a0001c0004t0003g0331a0001c0004t0003g0333others(32): Show | 36 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1380-177G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27541296 | ||||||
chr8:27541594 | G | A | 7 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0316others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449+52G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541594 | ||||||
chr8:27541656 | G | A | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449+114G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541656 | ||||||
chr8:27541909 | A | G | 1 | a0001c0002t0002g0232 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1449+367A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541909 | ||||||
chr8:27541957 | C | A | 2 | a0003c0007t0004g0312a0003c0007t0004g0313 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1449+415C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541957 | ||||||
chr8:27542001 | G | C | 49 | a0001c0005t0003g0036a0001c0005t0003g0144a0001c0005t0003g0168others(46): Show | 53 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1449+459G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542001 | ||||||
chr8:27542187 | A | G | 202 | a0001c0001t0001g0012a0001c0002t0002g0010a0001c0002t0002g0017others(199): Show | 209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1449+645A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542187 | ||||||
chr8:27542314 | A | C | 5 | a0001c0013t0002g0019a0001c0013t0002g0273a0001c0013t0006g0020others(2): Show | 5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+772A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542314 | ||||||
chr8:27542494 | A | G | 1 | a0003c0006t0002g0310 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1449+952A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542494 | ||||||
chr8:27542527 | G | A | 59 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(56): Show | 64 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1449+985G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542527 | ||||||
chr8:27542527 | G | C | 5 | a0007c0012t0001g0299a0007c0012t0001g0301a0007c0012t0001g0302others(2): Show | 5 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+985G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542527 | ||||||
chr8:27542551 | G | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0176others(19): Show | 24 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1449+1009G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542551 | ||||||
chr8:27542574 | G | A | 3 | a0003c0007t0008g0306a0003c0007t0008g0307a0003c0007t0012g0318 | 3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1449+1032G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542574 | ||||||
chr8:27542711 | G | T | 2 | a0003c0006t0002g0310a0003c0006t0002g0311 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1450-1038G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542711 | ||||||
chr8:27542849 | G | A | 3 | a0003c0007t0008g0306a0003c0007t0008g0307a0003c0007t0012g0318 | 3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1450-900G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542849 | ||||||
chr8:27543006 | T | TC | 33 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0091others(30): Show | 33 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1450-734dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 27543006 | |||||
chr8:27543006 | TC | T | 169 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(166): Show | 175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1450-734delC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 27543006 | |||||
chr8:27543012 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1450-737C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543012 | ||||||
chr8:27543013 | C | A | 8 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(5): Show | 8 | HG01516.hp1 HG01517.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1450-736C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543013 | ||||||
chr8:27543015 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1450-734C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543015 | ||||||
chr8:27543023 | G | A | 72 | a0001c0002t0002g0010a0001c0002t0002g0017a0001c0002t0002g0018others(69): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1450-726G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543023 | ||||||
chr8:27543075 | A | C | 80 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(77): Show | 85 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1450-674A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543075 | ||||||
chr8:27543087 | C | T | 80 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(77): Show | 85 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1450-662C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543087 | ||||||
chr8:27543142 | G | A | 1 | a0006c0020t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1450-607G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543142 | ||||||
chr8:27543165 | A | G | 53 | a0001c0005t0003g0036a0001c0005t0003g0082a0001c0005t0003g0083others(50): Show | 57 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1450-584A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543165 | ||||||
chr8:27543324 | A | C | 1 | a0001c0001t0006g0093 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1450-425A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543324 | ||||||
chr8:27543386 | T | G | 11 | a0003c0006t0002g0350a0003c0006t0002g0351a0003c0006t0002g0352others(8): Show | 11 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1450-363T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543386 | ||||||
chr8:27543441 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1450-308G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543441 | ||||||
chr8:27543490 | A | G | 1 | a0002c0003t0003g0051 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1450-259A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543490 | ||||||
chr8:27543506 | T | G | 1 | a0013c0028t0001g0147 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1450-243T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543506 | ||||||
chr8:27543616 | G | A | 3 | a0003c0007t0004g0314a0003c0007t0004g0315a0003c0007t0004g0321 | 3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1450-133G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543616 | ||||||
chr8:27543625 | G | A | 61 | a0001c0004t0003g0011a0001c0004t0003g0322a0001c0004t0003g0323others(58): Show | 66 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1450-124G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543625 | ||||||
chr8:27543849 | C | T | 2 | a0001c0013t0002g0019a0001c0013t0006g0020 | 2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1530+20C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27543849 | ||||||
chr8:27543864 | C | T | 2 | a0001c0005t0003g0168a0002c0003t0003g0049 | 2 | HG00408.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1530+35C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27543864 | ||||||
chr8:27543900 | C | T | 2 | a0001c0002t0002g0269a0001c0002t0002g0277 | 2 | HG02129.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1530+71C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27543900 | ||||||
chr8:27544087 | C | A | 7 | a0001c0005t0002g0077a0001c0005t0002g0078a0001c0005t0002g0079others(4): Show | 7 | HG02486.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1531-99C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27544087 | ||||||
chr8:27544105 | C | T | 7 | a0001c0004t0003g0331a0001c0004t0003g0333a0001c0004t0003g0335others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-81C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27544105 |