Item | Value |
---|---|
geneid | 2046 |
ensemblid | ENSG00000070886.12 |
hgncid | 3391 |
symbol | EPHA8 |
name | EPH receptor A8 |
refseq_nuc | NM_020526.5 |
refseq_prot | NP_065387.1 |
ensembl_nuc | ENST00000166244.8 |
ensembl_prot | ENSP00000166244.3 |
mane_status | MANE Select |
chr | chr1 |
start | 22563489 |
end | 22603595 |
strand | + |
ver | v1.2 |
region | chr1:22563489-22603595 |
region5000 | chr1:22558489-22608595 |
regionname0 | EPHA8_chr1_22563489_22603595 |
regionname5000 | EPHA8_chr1_22558489_22608595 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 8 | 0 | 2 | 6 | 0 | 0 | 5 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001 | 1/0 | 1005 | 265 | 67 | 62 | 89 | 12 | 34 | 61 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002 | 0/1 | 1005 | 44 | 12 | 10 | 15 | 1 | 5 | 13 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0003 | 0/0 | 1005 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0004 | 0/0 | 1005 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0005 | 0/0 | 1005 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0006 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0007 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0008 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0009 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0010 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0011 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0012 | 0/0 | 1005 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0013 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0014 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0015 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0016 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0017 | 0/0 | 1005 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0018 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3018 | 150 | 34 | 29 | 66 | 7 | 13 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0002 | 0/0 | 3018 | 58 | 21 | 19 | 7 | 1 | 10 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0003 | 0/0 | 3018 | 26 | 0 | 9 | 12 | 1 | 4 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0004 | 0/1 | 3018 | 15 | 11 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0005 | 0/0 | 3018 | 12 | 0 | 1 | 8 | 0 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0006 | 0/0 | 3018 | 8 | 0 | 3 | 0 | 3 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0007 | 0/0 | 3019 | 6 | 0 | 2 | 4 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0008 | 0/0 | 3018 | 5 | 0 | 1 | 0 | 1 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0009 | 0/0 | 3018 | 5 | 2 | 3 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0010 | 0/0 | 3018 | 4 | 0 | 1 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0011 | 0/0 | 3018 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0012 | 0/0 | 3018 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0013 | 0/0 | 3018 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0014 | 0/0 | 3018 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0015 | 0/0 | 3018 | 2 | 0 | 1 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0016 | 0/0 | 3018 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0017 | 0/0 | 3018 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0018 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0019 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0020 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0021 | 0/0 | 3018 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0022 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0023 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0024 | 0/0 | 2998 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0025 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0026 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0027 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0028 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0029 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0030 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0031 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0032 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0033 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0034 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0035 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0036 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0037 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0038 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0039 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0040 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0041 | 0/0 | 3007 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0042 | 0/0 | 3019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0043 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0044 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0045 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0046 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
c0047 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2002 | 91 | 0 | 18 | 54 | 6 | 12 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0002 | 0/0 | 1997 | 45 | 18 | 9 | 12 | 1 | 5 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0003 | 0/0 | 2002 | 40 | 19 | 6 | 12 | 0 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0004 | 0/0 | 1997 | 27 | 10 | 9 | 3 | 1 | 4 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0005 | 0/0 | 2002 | 15 | 2 | 6 | 3 | 3 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0006 | 0/0 | 2003 | 15 | 0 | 9 | 2 | 0 | 4 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0007 | 0/0 | 1997 | 15 | 0 | 5 | 8 | 1 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0008 | 0/0 | 1997 | 14 | 6 | 2 | 2 | 0 | 4 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0009 | 0/1 | 2002 | 9 | 2 | 0 | 5 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0010 | 0/0 | 1997 | 5 | 4 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0011 | 0/0 | 1997 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0012 | 0/0 | 1998 | 5 | 1 | 2 | 0 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0013 | 0/0 | 2002 | 4 | 3 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0014 | 0/0 | 2002 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0015 | 0/0 | 2003 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0016 | 0/0 | 1997 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0017 | 0/0 | 1997 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0018 | 0/0 | 2002 | 2 | 1 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0019 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0020 | 0/0 | 2002 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0021 | 0/0 | 2002 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0022 | 0/0 | 1997 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0023 | 0/0 | 1997 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0024 | 0/0 | 1997 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0025 | 0/0 | 1997 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0026 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0027 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0028 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0029 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0030 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0031 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0032 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0033 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0034 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0035 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0036 | 0/0 | 1997 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0037 | 0/0 | 1997 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0038 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0039 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0040 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0041 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0042 | 0/0 | 1997 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0043 | 0/0 | 1997 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0044 | 0/0 | 1997 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0045 | 0/0 | 1997 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0046 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0047 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0048 | 0/0 | 1997 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
t0049 | 0/0 | 2002 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0015 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0007 | 0/0 | 3019 | 6 | 0 | 2 | 4 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0000c0041 | 0/0 | 3007 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0000c0042 | 0/0 | 3019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0001 | 1/0 | 3018 | 150 | 34 | 29 | 66 | 7 | 13 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0002 | 0/0 | 3018 | 58 | 21 | 19 | 7 | 1 | 10 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0005 | 0/0 | 3018 | 12 | 0 | 1 | 8 | 0 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0006 | 0/0 | 3018 | 8 | 0 | 3 | 0 | 3 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0008 | 0/0 | 3018 | 5 | 0 | 1 | 0 | 1 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0009 | 0/0 | 3018 | 5 | 2 | 3 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0010 | 0/0 | 3018 | 4 | 0 | 1 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0011 | 0/0 | 3018 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0013 | 0/0 | 3018 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0015 | 0/0 | 3018 | 2 | 0 | 1 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0016 | 0/0 | 3018 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0017 | 0/0 | 3018 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0020 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0021 | 0/0 | 3018 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0022 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0027 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0028 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0033 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0045 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0001c0046 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0002c0003 | 0/0 | 3018 | 26 | 0 | 9 | 12 | 1 | 4 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0002c0004 | 0/1 | 3018 | 15 | 11 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0002c0037 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0002c0040 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0002c0043 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0003c0014 | 0/0 | 3018 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0003c0018 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0003c0047 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0004c0012 | 0/0 | 3018 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0004c0044 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0005c0019 | 0/0 | 3018 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0006c0038 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0007c0023 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0008c0034 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0009c0039 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0010c0024 | 0/0 | 2998 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0011c0025 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0012c0029 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0013c0032 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0014c0026 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0015c0031 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0016c0030 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0017c0036 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 | |
a0018c0035 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0007t0001 | 0/0 | 5020 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0000c0007t0003 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0000c0007t0010 | 0/0 | 5015 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0000c0007t0035 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0000c0041t0001 | 0/0 | 5008 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0000c0042t0003 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0001 | 1/0 | 5019 | 84 | 0 | 17 | 49 | 5 | 12 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0002 | 0/0 | 5014 | 6 | 4 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0003 | 0/0 | 5019 | 22 | 14 | 4 | 4 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0005 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0007 | 0/0 | 5014 | 13 | 0 | 3 | 8 | 1 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0008 | 0/0 | 5014 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0009 | 0/0 | 5019 | 4 | 2 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0010 | 0/0 | 5014 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0016 | 0/0 | 5014 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0018 | 0/0 | 5019 | 2 | 1 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0019 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0024 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0025 | 0/0 | 5014 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0027 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0029 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0033 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0001t0036 | 0/0 | 5014 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0002 | 0/0 | 5014 | 7 | 7 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0003 | 0/0 | 5019 | 2 | 1 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0004 | 0/0 | 5014 | 20 | 5 | 8 | 3 | 1 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0005 | 0/0 | 5019 | 7 | 2 | 3 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0006 | 0/0 | 5020 | 10 | 0 | 7 | 2 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0007 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0008 | 0/0 | 5014 | 3 | 0 | 0 | 0 | 0 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0010 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0022 | 0/0 | 5014 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0026 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0039 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0040 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0044 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0002t0045 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0005t0003 | 0/0 | 5019 | 8 | 0 | 1 | 5 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0005t0020 | 0/0 | 5019 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0005t0028 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0005t0049 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0006t0004 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0006t0005 | 0/0 | 5019 | 7 | 0 | 3 | 0 | 3 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0008t0006 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0008t0012 | 0/0 | 5015 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0008t0021 | 0/0 | 5019 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0009t0001 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0009t0003 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0009t0013 | 0/0 | 5019 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0010t0002 | 0/0 | 5014 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0010t0007 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0010t0009 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0010t0042 | 0/0 | 5014 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0011t0008 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0011t0010 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0011t0038 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0013t0017 | 0/0 | 5014 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0015t0008 | 0/0 | 5014 | 2 | 0 | 1 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0016t0006 | 0/0 | 5020 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0017t0008 | 0/0 | 5014 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0020t0012 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0020t0048 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0021t0012 | 0/0 | 5015 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0022t0004 | 0/0 | 5014 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0027t0003 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0028t0003 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0033t0006 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0045t0019 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0001c0046t0037 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0003t0002 | 0/0 | 5014 | 22 | 0 | 6 | 11 | 1 | 4 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0003t0023 | 0/0 | 5014 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0003t0031 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0003t0043 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0004t0009 | 0/1 | 5019 | 3 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0004t0011 | 0/0 | 5014 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0004t0014 | 0/0 | 5019 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0004t0030 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0004t0032 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0004t0034 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0004t0041 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0037t0002 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0040t0009 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0002c0043t0002 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0003c0014t0015 | 0/0 | 5020 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0003c0018t0003 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0003c0018t0047 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0003c0047t0013 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0004c0012t0002 | 0/0 | 5014 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0004c0044t0002 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0005c0019t0004 | 0/0 | 5014 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0006c0038t0024 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0007c0023t0002 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0008c0034t0002 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0009c0039t0003 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0010c0024t0046 | 0/0 | 4995 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0011c0025t0003 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0012c0029t0001 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0013c0032t0006 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0014c0026t0001 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0015c0031t0004 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0016c0030t0004 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0017c0036t0002 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
a0018c0035t0008 | 0/0 | 5014 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | copy fasta | chr1 | 22558489 | 22608595 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0000c0007t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0000c0007t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0000c0007t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0000c0007t0010g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0000c0007t0035g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0000c0041t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0000c0042t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0185 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0016g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0016g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0018g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0018g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0019g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0024g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0025g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0027g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0029g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0033g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0001t0036g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0005g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0008g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0008g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0008g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0022g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0022g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0026g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0039g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0040g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0044g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0002t0045g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0020g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0028g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0005t0049g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0006t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0008t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0008t0012g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0008t0021g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0008t0021g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0009t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0009t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0009t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0009t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0009t0013g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0010t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0010t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0010t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0010t0042g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0011t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0011t0010g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0011t0038g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0013t0017g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0013t0017g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0013t0017g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0015t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0015t0008g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0016t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0016t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0017t0008g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0017t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0020t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0020t0048g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0021t0012g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0021t0012g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0022t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0022t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0027t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0028t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0033t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0045t0019g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0001c0046t0037g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0023g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0023g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0031g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0003t0043g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0009g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0014g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0030g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0032g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0034g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0004t0041g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0037t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0040t0009g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0002c0043t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0003c0014t0015g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0003c0014t0015g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0003c0018t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0003c0018t0047g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0003c0047t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0004c0012t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0004c0012t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0004c0044t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0005c0019t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0005c0019t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0006c0038t0024g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0007c0023t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0008c0034t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0009c0039t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0010c0024t0046g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0011c0025t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0012c0029t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0013c0032t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0014c0026t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0015c0031t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0016c0030t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0017c0036t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
a0018c0035t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0101 | EUR | GBR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00099 | hp2 | a0001 | c0001 | t0018 | g0227 | EUR | GBR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00140 | hp1 | a0001 | c0006 | t0005 | g0285 | EUR | GBR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00140 | hp2 | a0002 | c0003 | t0002 | g0083 | EUR | GBR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00323 | hp1 | a0001 | c0006 | t0005 | g0283 | EUR | FIN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00438 | hp2 | a0001 | c0002 | t0004 | g0107 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00597 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0072 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00639 | hp1 | a0001 | c0002 | t0006 | g0208 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00639 | hp2 | a0001 | c0006 | t0005 | g0282 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00642 | hp1 | a0003 | c0014 | t0015 | g0023 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00642 | hp2 | a0002 | c0003 | t0002 | g0002 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00733 | hp1 | a0002 | c0003 | t0002 | g0002 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00733 | hp2 | a0001 | c0008 | t0021 | g0034 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00735 | hp1 | a0000 | c0007 | t0010 | g0158 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00735 | hp2 | a0001 | c0005 | t0003 | g0037 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00738 | hp1 | a0001 | c0015 | t0008 | g0119 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0111 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01069 | hp1 | a0001 | c0009 | t0003 | g0049 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01070 | hp2 | a0001 | c0002 | t0005 | g0022 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0022 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01074 | hp1 | a0001 | c0006 | t0005 | g0212 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01074 | hp2 | a0002 | c0003 | t0043 | g0182 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0123 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01099 | hp1 | a0002 | c0003 | t0002 | g0002 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01099 | hp2 | a0000 | c0007 | t0035 | g0006 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01106 | hp1 | a0001 | c0046 | t0037 | g0297 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01106 | hp2 | a0001 | c0001 | t0025 | g0157 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01109 | hp1 | a0018 | c0035 | t0008 | g0155 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01169 | hp2 | a0001 | c0006 | t0005 | g0207 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01175 | hp1 | a0001 | c0001 | t0007 | g0102 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01175 | hp2 | a0015 | c0031 | t0004 | g0126 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01192 | hp2 | a0001 | c0021 | t0012 | g0104 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01243 | hp1 | a0001 | c0009 | t0013 | g0046 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01243 | hp2 | a0001 | c0001 | t0016 | g0169 | AMR | PUR | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01255 | hp1 | a0001 | c0009 | t0001 | g0223 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01255 | hp2 | a0001 | c0033 | t0006 | g0213 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01256 | hp2 | a0001 | c0002 | t0006 | g0295 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0116 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01257 | hp2 | a0002 | c0003 | t0002 | g0008 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01258 | hp2 | a0002 | c0003 | t0002 | g0008 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01346 | hp1 | a0002 | c0003 | t0023 | g0087 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01346 | hp2 | a0001 | c0001 | t0029 | g0195 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01358 | hp1 | a0001 | c0002 | t0004 | g0125 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0115 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01361 | hp1 | a0002 | c0037 | t0002 | g0078 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01433 | hp1 | a0001 | c0002 | t0006 | g0100 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01496 | hp1 | a0002 | c0003 | t0023 | g0088 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01496 | hp2 | a0001 | c0002 | t0004 | g0113 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01515 | hp2 | a0001 | c0006 | t0005 | g0284 | EUR | IBS | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0132 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01891 | hp1 | a0001 | c0020 | t0012 | g0024 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01928 | hp1 | a0002 | c0003 | t0002 | g0077 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01928 | hp2 | a0001 | c0002 | t0006 | g0014 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01943 | hp1 | a0001 | c0002 | t0004 | g0128 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01943 | hp2 | a0001 | c0002 | t0005 | g0267 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01952 | hp2 | a0001 | c0002 | t0004 | g0112 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01975 | hp2 | a0001 | c0002 | t0006 | g0014 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01978 | hp1 | a0001 | c0002 | t0004 | g0114 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01978 | hp2 | a0013 | c0032 | t0006 | g0253 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01981 | hp2 | a0001 | c0021 | t0012 | g0105 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01993 | hp2 | a0001 | c0002 | t0004 | g0110 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02015 | hp1 | a0001 | c0001 | t0009 | g0237 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0138 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02027 | hp2 | a0002 | c0003 | t0002 | g0091 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02040 | hp1 | a0001 | c0017 | t0008 | g0305 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02055 | hp2 | a0002 | c0004 | t0011 | g0180 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02071 | hp1 | a0000 | c0007 | t0001 | g0218 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02080 | hp2 | a0001 | c0002 | t0004 | g0163 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02129 | hp2 | a0001 | c0002 | t0006 | g0209 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02132 | hp1 | a0001 | c0001 | t0036 | g0109 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02145 | hp1 | a0004 | c0012 | t0002 | g0007 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02145 | hp2 | a0001 | c0002 | t0005 | g0064 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CDX | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02257 | hp1 | a0004 | c0012 | t0002 | g0025 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0065 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02258 | hp1 | a0011 | c0025 | t0003 | g0278 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02273 | hp1 | a0001 | c0010 | t0007 | g0080 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02273 | hp2 | a0001 | c0002 | t0006 | g0217 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02280 | hp1 | a0001 | c0002 | t0005 | g0063 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02293 | hp2 | a0001 | c0002 | t0006 | g0211 | AMR | PEL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0151 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02451 | hp2 | a0001 | c0045 | t0019 | g0047 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02572 | hp2 | a0001 | c0002 | t0004 | g0067 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02602 | hp1 | a0001 | c0002 | t0008 | g0130 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02602 | hp2 | a0001 | c0002 | t0004 | g0141 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02615 | hp1 | a0001 | c0002 | t0039 | g0300 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02615 | hp2 | a0001 | c0002 | t0022 | g0156 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0062 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02622 | hp2 | a0001 | c0011 | t0008 | g0134 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02630 | hp1 | a0005 | c0019 | t0004 | g0148 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02647 | hp1 | a0001 | c0009 | t0013 | g0045 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02683 | hp2 | a0017 | c0036 | t0002 | g0071 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02723 | hp2 | a0001 | c0011 | t0010 | g0142 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02735 | hp1 | a0001 | c0002 | t0006 | g0214 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02735 | hp2 | a0001 | c0002 | t0008 | g0121 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02738 | hp1 | a0001 | c0006 | t0004 | g0288 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02809 | hp1 | a0006 | c0038 | t0024 | g0161 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02809 | hp2 | a0004 | c0044 | t0002 | g0296 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02818 | hp1 | a0001 | c0002 | t0003 | g0280 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02818 | hp2 | a0002 | c0004 | t0032 | g0179 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0127 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02895 | hp1 | a0001 | c0002 | t0026 | g0240 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0152 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02896 | hp1 | a0001 | c0001 | t0016 | g0166 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0153 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02922 | hp1 | a0003 | c0047 | t0013 | g0048 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02922 | hp2 | a0004 | c0012 | t0002 | g0007 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02965 | hp1 | a0001 | c0001 | t0010 | g0168 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02965 | hp2 | a0001 | c0020 | t0048 | g0095 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02970 | hp1 | a0001 | c0009 | t0013 | g0044 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02970 | hp2 | a0001 | c0011 | t0038 | g0069 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02976 | hp1 | a0001 | c0001 | t0010 | g0170 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02976 | hp2 | a0002 | c0004 | t0014 | g0003 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03041 | hp1 | a0001 | c0028 | t0003 | g0243 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0221 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03098 | hp2 | a0002 | c0004 | t0041 | g0174 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03130 | hp1 | a0001 | c0002 | t0010 | g0165 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03139 | hp1 | a0002 | c0004 | t0011 | g0177 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03139 | hp2 | a0002 | c0004 | t0014 | g0003 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03195 | hp1 | a0002 | c0004 | t0011 | g0178 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03195 | hp2 | a0016 | c0030 | t0004 | g0066 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03209 | hp2 | a0001 | c0001 | t0019 | g0261 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03225 | hp2 | a0001 | c0001 | t0024 | g0162 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0117 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03453 | hp2 | a0002 | c0043 | t0002 | g0298 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03491 | hp1 | a0001 | c0015 | t0008 | g0140 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03491 | hp2 | a0001 | c0008 | t0012 | g0010 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03492 | hp1 | a0001 | c0008 | t0012 | g0010 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0146 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03516 | hp2 | a0002 | c0004 | t0014 | g0003 | AFR | ESN | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03540 | hp1 | a0001 | c0001 | t0033 | g0171 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03579 | hp1 | a0002 | c0004 | t0011 | g0061 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03654 | hp1 | a0001 | c0008 | t0006 | g0040 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03654 | hp2 | a0001 | c0002 | t0044 | g0124 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03669 | hp1 | a0001 | c0002 | t0045 | g0172 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03669 | hp2 | a0001 | c0016 | t0006 | g0203 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0206 | SAS | STU | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03688 | hp2 | a0001 | c0005 | t0049 | g0039 | SAS | STU | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03704 | hp1 | a0001 | c0005 | t0003 | g0038 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03704 | hp2 | a0002 | c0040 | t0009 | g0030 | SAS | PJL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03831 | hp1 | a0002 | c0003 | t0002 | g0092 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03831 | hp2 | a0001 | c0002 | t0008 | g0118 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03834 | hp1 | a0001 | c0006 | t0005 | g0286 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03834 | hp2 | a0001 | c0016 | t0006 | g0205 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03927 | hp1 | a0002 | c0003 | t0002 | g0084 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03927 | hp2 | a0002 | c0003 | t0002 | g0086 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03942 | hp2 | a0001 | c0002 | t0004 | g0131 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG04115 | hp1 | a0001 | c0002 | t0004 | g0120 | SAS | STU | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG04115 | hp2 | a0002 | c0003 | t0002 | g0075 | SAS | STU | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG04204 | hp2 | a0001 | c0005 | t0003 | g0033 | SAS | STU | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18522 | hp1 | a0001 | c0001 | t0016 | g0167 | AFR | YRI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18522 | hp2 | a0001 | c0002 | t0022 | g0159 | AFR | YRI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18612 | hp1 | a0002 | c0003 | t0002 | g0085 | EAS | CHB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18747 | hp2 | a0014 | c0026 | t0001 | g0229 | EAS | CHB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18906 | hp1 | a0007 | c0023 | t0002 | g0012 | AFR | YRI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18906 | hp2 | a0002 | c0004 | t0011 | g0181 | AFR | YRI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18939 | hp1 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18939 | hp2 | a0001 | c0001 | t0027 | g0144 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18940 | hp2 | a0002 | c0003 | t0002 | g0097 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18945 | hp2 | a0001 | c0005 | t0003 | g0035 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18948 | hp1 | a0001 | c0002 | t0005 | g0074 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18950 | hp2 | a0002 | c0003 | t0002 | g0096 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18952 | hp2 | a0002 | c0003 | t0031 | g0081 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18957 | hp2 | a0001 | c0013 | t0017 | g0307 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18959 | hp1 | a0000 | c0007 | t0001 | g0269 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18964 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18965 | hp1 | a0001 | c0010 | t0042 | g0094 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18966 | hp2 | a0002 | c0004 | t0009 | g0188 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18967 | hp2 | a0001 | c0013 | t0017 | g0308 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18970 | hp2 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18975 | hp1 | a0009 | c0039 | t0003 | g0310 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18979 | hp1 | a0002 | c0004 | t0030 | g0254 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18979 | hp2 | a0000 | c0007 | t0003 | g0197 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18980 | hp2 | a0001 | c0005 | t0020 | g0043 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18981 | hp1 | a0000 | c0042 | t0003 | g0106 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18985 | hp1 | a0000 | c0007 | t0001 | g0005 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18985 | hp2 | a0000 | c0041 | t0001 | g0031 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18986 | hp1 | a0001 | c0005 | t0003 | g0032 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18992 | hp1 | a0002 | c0003 | t0002 | g0082 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18992 | hp2 | a0001 | c0005 | t0020 | g0042 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA18995 | hp2 | a0001 | c0002 | t0006 | g0215 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19004 | hp1 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0268 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19007 | hp1 | a0002 | c0003 | t0002 | g0090 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19007 | hp2 | a0001 | c0002 | t0005 | g0073 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19010 | hp2 | a0001 | c0002 | t0004 | g0129 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19012 | hp1 | a0002 | c0003 | t0002 | g0079 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19012 | hp2 | a0001 | c0001 | t0007 | g0099 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0145 | AFR | LWK | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0149 | AFR | LWK | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19043 | hp1 | a0005 | c0019 | t0004 | g0147 | AFR | LWK | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19043 | hp2 | a0001 | c0001 | t0018 | g0265 | AFR | LWK | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19057 | hp1 | a0001 | c0013 | t0017 | g0306 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19057 | hp2 | a0001 | c0005 | t0003 | g0055 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19058 | hp2 | a0001 | c0005 | t0028 | g0052 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19063 | hp1 | a0001 | c0010 | t0009 | g0029 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19064 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19068 | hp1 | a0001 | c0005 | t0003 | g0053 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19074 | hp2 | a0001 | c0017 | t0008 | g0304 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19085 | hp1 | a0002 | c0003 | t0002 | g0089 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19087 | hp2 | a0001 | c0005 | t0003 | g0036 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19088 | hp2 | a0002 | c0004 | t0009 | g0216 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19090 | hp1 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19090 | hp2 | a0001 | c0001 | t0009 | g0257 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19091 | hp1 | a0001 | c0010 | t0002 | g0093 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19240 | hp1 | a0003 | c0018 | t0047 | g0160 | AFR | YRI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0150 | AFR | YRI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20129 | hp1 | a0003 | c0014 | t0015 | g0023 | AFR | ASW | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0068 | AFR | ASW | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20752 | hp1 | a0012 | c0029 | t0001 | g0013 | EUR | TSI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0122 | EUR | TSI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20805 | hp2 | a0001 | c0008 | t0021 | g0054 | EUR | TSI | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | GIH | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01123 | hp1 | a0001 | c0002 | t0007 | g0173 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02486 | hp1 | a0003 | c0014 | t0015 | g0302 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02486 | hp2 | a0003 | c0018 | t0003 | g0289 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02559 | hp1 | a0002 | c0004 | t0034 | g0164 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG02559 | hp2 | a0001 | c0022 | t0004 | g0028 | AFR | ACB | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03471 | hp1 | a0001 | c0002 | t0040 | g0060 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0301 | AFR | MSL | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG06807 | hp1 | a0001 | c0022 | t0004 | g0027 | AFR | USA | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
HG06807 | hp2 | a0001 | c0027 | t0003 | g0244 | AFR | USA | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | USA | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA20300 | hp2 | a0001 | c0001 | t0025 | g0026 | AFR | USA | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA21309 | hp1 | a0008 | c0034 | t0002 | g0176 | AFR | LWK | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
NA21309 | hp2 | a0010 | c0024 | t0046 | g0175 | AFR | LWK | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
homoSapiens_chm13v2 | hp1 | a0002 | c0004 | t0009 | g0287 | REF | REF | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0185 | REF | REF | EPHA8_chr1_22558489_22608595 | EPHA8 | chr1 | 22558489 | 22608595 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:22563617 | CGCCCG | C | 14 | a0000a0001a0002others(11): Show | 146 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(143): Show |
start_retained_variant | MODIFIER | c.-5_-1delCGGCC | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 22563617 | |||||
chr1:22576288 | C | G | 1 | a0006 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.231C>G | p.Ser77Arg | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/17 | 378/5019 | 231/3018 | 77/1005 | chr1 | 22576288 | ||
chr1:22576683 | G | A | 1 | a0007 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.626G>A | p.Arg209His | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/17 | 773/5019 | 626/3018 | 209/1005 | chr1 | 22576683 | ||
chr1:22586558 | C | T | 2 | a0005a0018 | 3 | HG01109.hp1 HG02630.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.902C>T | p.Ala301Val | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/17 | 1049/5019 | 902/3018 | 301/1005 | chr1 | 22586558 | ||
chr1:22586618 | C | T | 2 | a0003a0008 | 7 | HG00642.hp1 HG02486.hp1 HG02486.hp2 others(4): Show |
missense_variant | MODERATE | c.962C>T | p.Pro321Leu | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/17 | 1109/5019 | 962/3018 | 321/1005 | chr1 | 22586618 | ||
chr1:22588893 | C | A | 1 | a0009 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.1002C>A | p.Asn334Lys | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/17 | 1149/5019 | 1002/3018 | 334/1005 | chr1 | 22588893 | ||
chr1:22589036 | GCACCCGC others(13): Show |
G | 1 | a0010 | 1 | NA21309.hp2 | frameshift_variant | HIGH | c.1146_1165delCACCCG others(14): Show |
p.Thr383fs | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/17 | 1293/5019 | 1146/3018 | 382/1005 | chr1 | 22589036 | ||
chr1:22589134 | G | A | 1 | a0011 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1243G>A | p.Val415Ile | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/17 | 1390/5019 | 1243/3018 | 415/1005 | chr1 | 22589134 | ||
chr1:22593536 | C | G | 1 | a0012 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1453C>G | p.Gln485Glu | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/17 | 1600/5019 | 1453/3018 | 485/1005 | chr1 | 22593536 | ||
chr1:22593616 | G | T | 1 | a0013 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1533G>T | p.Gln511His | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/17 | 1680/5019 | 1533/3018 | 511/1005 | chr1 | 22593616 | ||
chr1:22595289 | G | A | 1 | a0014 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1663G>A | p.Val555Met | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/17 | 1810/5019 | 1663/3018 | 555/1005 | chr1 | 22595289 | ||
chr1:22597380 | G | C | 3 | a0002a0008a0017 | 46 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(43): Show |
missense_variant | MODERATE | c.1834G>C | p.Glu612Gln | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 10/17 | 1981/5019 | 1834/3018 | 612/1005 | chr1 | 22597380 | ||
chr1:22598153 | C | T | 1 | a0004 | 4 | HG02145.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.2119C>T | p.Arg707Cys | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/17 | 2266/5019 | 2119/3018 | 707/1005 | chr1 | 22598153 | ||
chr1:22598984 | GGTGTCTG others(5): Show |
G | 1 | a0000 | 1 | NA18985.hp2 | disruptive_inframe_deletion | MODERATE | c.2327_2338delTGTCTG others(6): Show |
p.Val776_Phe779del | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/17 | 2474/5019 | 2327/3018 | 776/1005 | INFO_REALIGN_3_PRIME | chr1 | 22598984 | |
chr1:22601397 | C | T | 1 | a0015 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.2827C>T | p.Arg943Cys | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/17 | 2974/5019 | 2827/3018 | 943/1005 | chr1 | 22601397 | ||
chr1:22601406 | C | CG | 1 | a0000 | 8 | HG00735.hp1 HG01099.hp2 HG02071.hp1 others(5): Show |
frameshift_variant | HIGH | c.2838dupG | p.Tyr947fs | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/17 | 2986/5019 | 2839/3018 | 947/1005 | INFO_REALIGN_3_PRIME | chr1 | 22601406 | |
chr1:22601413 | G | A | 1 | a0018 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2843G>A | p.Arg948Gln | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/17 | 2990/5019 | 2843/3018 | 948/1005 | chr1 | 22601413 | ||
chr1:22601637 | G | A | 1 | a0016 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.2914G>A | p.Ala972Thr | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 3061/5019 | 2914/3018 | 972/1005 | chr1 | 22601637 | ||
chr1:22601655 | A | G | 1 | a0017 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.2932A>G | p.Met978Val | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 3079/5019 | 2932/3018 | 978/1005 | chr1 | 22601655 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:22576279 | C | T | 14 | a0000c0041a0000c0042a0001c0005others(11): Show | 35 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(32): Show |
synonymous_variant | LOW | c.222C>T | p.Asn74Asn | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/17 | 369/5019 | 222/3018 | 74/1005 | chr1 | 22576279 | ||
chr1:22576609 | C | T | 5 | a0001c0010a0001c0020a0002c0003others(2): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
synonymous_variant | LOW | c.552C>T | p.Ala184Ala | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/17 | 699/5019 | 552/3018 | 184/1005 | chr1 | 22576609 | ||
chr1:22589001 | C | T | 2 | a0001c0013a0001c0017 | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
synonymous_variant | LOW | c.1110C>T | p.Pro370Pro | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/17 | 1257/5019 | 1110/3018 | 370/1005 | chr1 | 22589001 | ||
chr1:22589181 | G | A | 8 | a0000c0041a0000c0042a0001c0005others(5): Show | 26 | HG00733.hp2 HG00735.hp2 HG01192.hp2 others(23): Show |
synonymous_variant | LOW | c.1290G>A | p.Val430Val | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/17 | 1437/5019 | 1290/3018 | 430/1005 | chr1 | 22589181 | ||
chr1:22593411 | C | T | 22 | a0000c0041a0000c0042a0001c0002others(19): Show | 103 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(100): Show |
synonymous_variant | LOW | c.1401C>T | p.Asn467Asn | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 6/17 | 1548/5019 | 1401/3018 | 467/1005 | chr1 | 22593411 | ||
chr1:22593583 | C | T | 1 | a0001c0045 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1500C>T | p.Ser500Ser | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/17 | 1647/5019 | 1500/3018 | 500/1005 | chr1 | 22593583 | ||
chr1:22593601 | C | G | 2 | a0001c0006a0001c0013 | 11 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
synonymous_variant | LOW | c.1518C>G | p.Thr506Thr | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/17 | 1665/5019 | 1518/3018 | 506/1005 | chr1 | 22593601 | ||
chr1:22593607 | C | T | 1 | a0001c0033 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1524C>T | p.Tyr508Tyr | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/17 | 1671/5019 | 1524/3018 | 508/1005 | chr1 | 22593607 | ||
chr1:22598975 | G | A | 1 | a0001c0046 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.2316G>A | p.Leu772Leu | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/17 | 2463/5019 | 2316/3018 | 772/1005 | chr1 | 22598975 | ||
chr1:22599020 | C | T | 1 | a0001c0013 | 3 | NA18957.hp2 NA18967.hp2 NA19057.hp1 |
synonymous_variant | LOW | c.2361C>T | p.Asp787Asp | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/17 | 2508/5019 | 2361/3018 | 787/1005 | chr1 | 22599020 | ||
chr1:22600915 | G | A | 6 | a0000c0041a0000c0042a0001c0005others(3): Show | 19 | HG00735.hp2 HG00738.hp1 HG02040.hp1 others(16): Show |
synonymous_variant | LOW | c.2556G>A | p.Glu852Glu | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/17 | 2703/5019 | 2556/3018 | 852/1005 | chr1 | 22600915 | ||
chr1:22600933 | C | T | 1 | a0001c0028 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2574C>T | p.Pro858Pro | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/17 | 2721/5019 | 2574/3018 | 858/1005 | chr1 | 22600933 | ||
chr1:22601357 | C | T | 1 | a0001c0027 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2787C>T | p.Gly929Gly | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/17 | 2934/5019 | 2787/3018 | 929/1005 | chr1 | 22601357 | ||
chr1:22601645 | C | T | 1 | a0001c0016 | 2 | HG03669.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.2922C>T | p.Gly974Gly | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 3069/5019 | 2922/3018 | 974/1005 | chr1 | 22601645 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:22563514 | C | T | 1 | a0001c0005t0049 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-122C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | 122 | chr1 | 22563514 | |||||
chr1:22563534 | G | T | 1 | a0001c0020t0048 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | 102 | chr1 | 22563534 | |||||
chr1:22563557 | C | T | 1 | a0003c0018t0047 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | 79 | chr1 | 22563557 | |||||
chr1:22563568 | G | C | 1 | a0001c0002t0026 | 1 | HG02895.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | 68 | chr1 | 22563568 | |||||
chr1:22563582 | A | C | 58 | a0000c0007t0010a0000c0007t0035a0001c0001t0002others(55): Show | 147 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
5_prime_UTR_variant | MODIFIER | c.-54A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | 54 | chr1 | 22563582 | |||||
chr1:22563595 | G | A | 1 | a0002c0004t0032 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | 41 | chr1 | 22563595 | |||||
chr1:22563632 | G | C | 8 | a0000c0007t0010a0001c0001t0010a0001c0001t0016others(5): Show | 12 | HG00735.hp1 HG01243.hp2 HG02559.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-4G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/17 | 4 | chr1 | 22563632 | |||||
chr1:22601772 | A | G | 91 | a0000c0007t0003a0000c0007t0010a0000c0007t0035others(88): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*31A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 31 | chr1 | 22601772 | |||||
chr1:22601797 | G | T | 2 | a0001c0001t0025a0010c0024t0046 | 3 | HG01106.hp2 NA20300.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*56G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 56 | chr1 | 22601797 | |||||
chr1:22601812 | G | T | 1 | a0001c0001t0018 | 2 | HG00099.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*71G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 71 | chr1 | 22601812 | |||||
chr1:22601837 | A | G | 1 | a0001c0013t0017 | 3 | NA18957.hp2 NA18967.hp2 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*96A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 96 | chr1 | 22601837 | |||||
chr1:22601855 | C | T | 1 | a0003c0014t0015 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*114C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 114 | chr1 | 22601855 | |||||
chr1:22601856 | A | G | 57 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(54): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*115A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 115 | chr1 | 22601856 | |||||
chr1:22601917 | G | A | 1 | a0002c0004t0030 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 176 | chr1 | 22601917 | |||||
chr1:22602011 | A | G | 11 | a0001c0002t0006a0001c0002t0045a0001c0008t0006others(8): Show | 26 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*270A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 270 | chr1 | 22602011 | |||||
chr1:22602119 | G | A | 1 | a0001c0001t0027 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 378 | chr1 | 22602119 | |||||
chr1:22602134 | C | T | 2 | a0001c0009t0013a0003c0047t0013 | 4 | HG01243.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*393C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 393 | chr1 | 22602134 | |||||
chr1:22602135 | G | A | 1 | a0001c0001t0033 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 394 | chr1 | 22602135 | |||||
chr1:22602150 | C | T | 11 | a0001c0002t0006a0001c0002t0045a0001c0008t0006others(8): Show | 26 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*409C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 409 | chr1 | 22602150 | |||||
chr1:22602151 | G | A | 1 | a0001c0046t0037 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 410 | chr1 | 22602151 | |||||
chr1:22602163 | T | G | 2 | a0001c0002t0039a0001c0002t0040 | 2 | HG02615.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*422T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 422 | chr1 | 22602163 | |||||
chr1:22602178 | C | G | 1 | a0001c0001t0036 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*437C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 437 | chr1 | 22602178 | |||||
chr1:22602310 | G | A | 1 | a0002c0004t0041 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*569G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 569 | chr1 | 22602310 | |||||
chr1:22602320 | A | G | 57 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(54): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*579A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 579 | chr1 | 22602320 | |||||
chr1:22602402 | C | T | 11 | a0001c0002t0006a0001c0002t0045a0001c0008t0006others(8): Show | 26 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*661C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 661 | chr1 | 22602402 | |||||
chr1:22602446 | A | C | 1 | a0001c0011t0038 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*705A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 705 | chr1 | 22602446 | |||||
chr1:22602631 | C | T | 1 | a0001c0005t0020 | 2 | NA18980.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*890C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 890 | chr1 | 22602631 | |||||
chr1:22602661 | C | T | 1 | a0001c0001t0029 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 920 | chr1 | 22602661 | |||||
chr1:22602883 | A | G | 18 | a0001c0001t0005a0001c0001t0024a0001c0002t0004others(15): Show | 58 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1142A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1142 | chr1 | 22602883 | |||||
chr1:22602931 | C | G | 4 | a0002c0004t0011a0002c0004t0014a0002c0004t0032others(1): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1190C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1190 | chr1 | 22602931 | |||||
chr1:22602944 | C | T | 1 | a0001c0013t0017 | 3 | NA18957.hp2 NA18967.hp2 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1203C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1203 | chr1 | 22602944 | |||||
chr1:22603172 | C | A | 1 | a0001c0002t0044 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1431C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1431 | chr1 | 22603172 | |||||
chr1:22603229 | C | T | 2 | a0001c0001t0019a0001c0045t0019 | 2 | HG02451.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1488C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1488 | chr1 | 22603229 | |||||
chr1:22603248 | G | A | 2 | a0001c0001t0024a0006c0038t0024 | 2 | HG02809.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1507G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1507 | chr1 | 22603248 | |||||
chr1:22603259 | G | C | 1 | a0001c0010t0042 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1518G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1518 | chr1 | 22603259 | |||||
chr1:22603276 | C | T | 1 | a0002c0003t0023 | 2 | HG01346.hp1 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1535 | chr1 | 22603276 | |||||
chr1:22603365 | C | T | 1 | a0001c0005t0028 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1624 | chr1 | 22603365 | |||||
chr1:22603370 | T | TG | 10 | a0001c0002t0006a0001c0008t0006a0001c0008t0012others(7): Show | 24 | HG00639.hp1 HG00642.hp1 HG01192.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1638dupG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1639 | INFO_REALIGN_3_PRIME | chr1 | 22603370 | ||||
chr1:22603375 | G | C | 1 | a0002c0003t0043 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1634 | chr1 | 22603375 | |||||
chr1:22603406 | C | A | 1 | a0002c0003t0031 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1665C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1665 | chr1 | 22603406 | |||||
chr1:22603429 | C | G | 1 | a0001c0002t0040 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1688C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1688 | chr1 | 22603429 | |||||
chr1:22603551 | C | T | 2 | a0001c0009t0013a0003c0047t0013 | 4 | HG01243.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1810C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 17/17 | 1810 | chr1 | 22603551 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:22563858 | G | T | 1 | a0009c0039t0003g0310 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.94+129G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22563858 | ||||||
chr1:22563886 | G | A | 6 | a0001c0001t0025g0026a0001c0020t0012g0024a0001c0022t0004g0027others(3): Show | 7 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+157G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22563886 | ||||||
chr1:22564006 | G | C | 32 | a0000c0041t0001g0031a0001c0001t0001g0041a0001c0001t0001g0050others(29): Show | 32 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.94+277G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564006 | ||||||
chr1:22564071 | G | A | 1 | a0001c0002t0040g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.94+342G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564071 | ||||||
chr1:22564095 | G | A | 1 | a0002c0004t0011g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.94+366G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564095 | ||||||
chr1:22564164 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.94+435A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564164 | ||||||
chr1:22564315 | G | C | 2 | a0001c0001t0009g0062a0001c0002t0005g0063 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.94+586G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564315 | ||||||
chr1:22564343 | C | G | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+614C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564343 | ||||||
chr1:22564379 | T | A | 24 | a0000c0041t0001g0031a0001c0001t0001g0041a0001c0001t0001g0050others(21): Show | 24 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.94+650T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564379 | ||||||
chr1:22564625 | G | A | 1 | a0001c0002t0005g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.94+896G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564625 | ||||||
chr1:22564657 | C | T | 5 | a0001c0001t0001g0303a0001c0013t0017g0306a0001c0013t0017g0307others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+928C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564657 | ||||||
chr1:22564734 | C | T | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.94+1005C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564734 | ||||||
chr1:22564792 | C | T | 4 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301others(1): Show | 5 | HG01099.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1063C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564792 | ||||||
chr1:22564823 | C | G | 4 | a0001c0002t0005g0022a0001c0002t0005g0064a0003c0014t0015g0023others(1): Show | 6 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1094C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564823 | ||||||
chr1:22564916 | T | C | 168 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(165): Show | 178 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.94+1187T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564916 | ||||||
chr1:22564946 | C | T | 1 | a0001c0001t0003g0299 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+1217C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22564946 | ||||||
chr1:22565064 | CCACA | C | 11 | a0001c0009t0003g0049a0001c0009t0013g0044a0001c0009t0013g0045others(8): Show | 11 | HG01069.hp1 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+1342_94+1345del others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 22565064 | |||||
chr1:22565123 | A | G | 1 | a0002c0003t0043g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+1394A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565123 | ||||||
chr1:22565216 | C | T | 7 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(4): Show | 9 | HG02055.hp2 HG02818.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+1487C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565216 | ||||||
chr1:22565269 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.94+1540T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565269 | ||||||
chr1:22565472 | C | T | 298 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0001g0269others(295): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.94+1743C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565472 | ||||||
chr1:22565481 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.94+1752G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565481 | ||||||
chr1:22565554 | C | T | 1 | a0001c0002t0006g0295 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.94+1825C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565554 | ||||||
chr1:22565667 | G | T | 4 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(1): Show | 4 | NA18940.hp1 NA18945.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1938G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565667 | ||||||
chr1:22565676 | C | T | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94+1947C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565676 | ||||||
chr1:22565823 | G | T | 4 | a0001c0002t0007g0173a0001c0002t0045g0172a0002c0004t0041g0174others(1): Show | 4 | HG01123.hp1 HG03098.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+2094G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565823 | ||||||
chr1:22565889 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+2160C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565889 | ||||||
chr1:22565908 | G | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+2179G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565908 | ||||||
chr1:22565972 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.94+2243G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22565972 | ||||||
chr1:22566142 | T | C | 3 | a0001c0002t0004g0065a0001c0002t0004g0067a0016c0030t0004g0066 | 3 | HG02257.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.94+2413T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566142 | ||||||
chr1:22566176 | C | A | 1 | a0001c0002t0004g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94+2447C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566176 | ||||||
chr1:22566276 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.94+2547C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566276 | ||||||
chr1:22566361 | A | G | 9 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(6): Show | 9 | HG01243.hp2 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+2632A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566361 | ||||||
chr1:22566390 | G | A | 9 | a0001c0001t0002g0070a0001c0011t0038g0069a0002c0004t0011g0061others(6): Show | 11 | HG02055.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+2661G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566390 | ||||||
chr1:22566490 | C | A | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.94+2761C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566490 | ||||||
chr1:22566676 | C | A | 2 | a0001c0001t0001g0013a0012c0029t0001g0013 | 2 | HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.95-2613C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566676 | ||||||
chr1:22566797 | C | G | 1 | a0002c0043t0002g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.95-2492C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566797 | ||||||
chr1:22566801 | T | A | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.95-2488T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566801 | ||||||
chr1:22566835 | C | T | 1 | a0001c0002t0004g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.95-2454C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566835 | ||||||
chr1:22566976 | T | C | 4 | a0001c0002t0007g0173a0001c0002t0045g0172a0002c0004t0041g0174others(1): Show | 4 | HG01123.hp1 HG03098.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2313T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566976 | ||||||
chr1:22566978 | G | T | 2 | a0001c0001t0024g0162a0006c0038t0024g0161 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.95-2311G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566978 | ||||||
chr1:22566985 | C | T | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.95-2304C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22566985 | ||||||
chr1:22567050 | G | A | 47 | a0001c0001t0002g0070a0001c0001t0002g0098a0001c0001t0007g0072others(44): Show | 54 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.95-2239G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567050 | ||||||
chr1:22567076 | G | A | 1 | a0017c0036t0002g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.95-2213G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567076 | ||||||
chr1:22567091 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.95-2198T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567091 | ||||||
chr1:22567113 | C | A | 10 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(7): Show | 10 | HG01243.hp2 HG02559.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-2176C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567113 | ||||||
chr1:22567114 | G | A | 1 | a0001c0002t0040g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.95-2175G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567114 | ||||||
chr1:22567214 | G | A | 33 | a0001c0001t0007g0072a0001c0002t0005g0073a0001c0002t0005g0074others(30): Show | 37 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.95-2075G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567214 | ||||||
chr1:22567258 | ACCCATAC others(8): Show |
A | 4 | a0001c0002t0002g0012a0003c0018t0003g0289a0003c0018t0047g0160others(1): Show | 4 | HG02486.hp2 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2028_95-2014del others(15): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 22567258 | |||||
chr1:22567321 | A | T | 2 | a0001c0005t0020g0042a0001c0005t0020g0043 | 2 | NA18980.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.95-1968A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567321 | ||||||
chr1:22567415 | C | G | 99 | a0000c0007t0010g0158a0000c0007t0035g0006a0001c0001t0002g0070others(96): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.95-1874C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567415 | ||||||
chr1:22567443 | C | A | 94 | a0000c0007t0010g0158a0000c0007t0035g0006a0001c0001t0002g0070others(91): Show | 103 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.95-1846C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567443 | ||||||
chr1:22567476 | G | A | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.95-1813G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567476 | ||||||
chr1:22567526 | G | A | 2 | a0001c0022t0004g0027a0001c0022t0004g0028 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.95-1763G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567526 | ||||||
chr1:22567534 | G | A | 2 | a0001c0001t0001g0200a0001c0001t0007g0099 | 2 | NA18975.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.95-1755G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567534 | ||||||
chr1:22567555 | G | A | 1 | a0001c0001t0003g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.95-1734G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567555 | ||||||
chr1:22567616 | G | A | 1 | a0001c0020t0012g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.95-1673G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567616 | ||||||
chr1:22567825 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-1464G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567825 | ||||||
chr1:22567859 | A | G | 4 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(1): Show | 4 | NA18957.hp2 NA18967.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1430A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567859 | ||||||
chr1:22567860 | G | GA | 4 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(1): Show | 4 | NA18957.hp2 NA18967.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1429_95-1428ins others(1): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567860 | ||||||
chr1:22567863 | G | T | 4 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(1): Show | 4 | NA18957.hp2 NA18967.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1426G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567863 | ||||||
chr1:22567906 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.95-1383G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567906 | ||||||
chr1:22567970 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.95-1319T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22567970 | ||||||
chr1:22568009 | G | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0204a0001c0001t0001g0210others(18): Show | 27 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.95-1280G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568009 | ||||||
chr1:22568037 | C | T | 8 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(5): Show | 8 | HG01243.hp2 HG02896.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-1252C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568037 | ||||||
chr1:22568159 | A | C | 95 | a0000c0007t0010g0158a0000c0007t0035g0006a0001c0001t0002g0070others(92): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.95-1130A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568159 | ||||||
chr1:22568301 | A | G | 90 | a0000c0007t0010g0158a0000c0007t0035g0006a0001c0001t0002g0070others(87): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.95-988A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568301 | ||||||
chr1:22568445 | C | T | 4 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0022g0156others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-844C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568445 | ||||||
chr1:22568513 | C | T | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-776C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568513 | ||||||
chr1:22568515 | G | C | 35 | a0000c0007t0001g0218a0000c0041t0001g0031a0000c0042t0003g0106others(32): Show | 36 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.95-774G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568515 | ||||||
chr1:22568535 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.95-754C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568535 | ||||||
chr1:22568546 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.95-743A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568546 | ||||||
chr1:22568552 | G | T | 1 | a0001c0001t0008g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95-737G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568552 | ||||||
chr1:22568578 | T | G | 34 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0103others(31): Show | 35 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.95-711T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568578 | ||||||
chr1:22568585 | C | T | 4 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0022g0156others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-704C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568585 | ||||||
chr1:22568695 | G | A | 3 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148 | 3 | HG02630.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.95-594G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568695 | ||||||
chr1:22568752 | G | A | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.95-537G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568752 | ||||||
chr1:22568934 | T | G | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-355T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568934 | ||||||
chr1:22568984 | G | A | 9 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0036g0109others(6): Show | 9 | HG00438.hp2 HG00738.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-305G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568984 | ||||||
chr1:22568994 | A | G | 17 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0007g0173others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-295A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22568994 | ||||||
chr1:22569183 | G | A | 1 | a0001c0002t0004g0065 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.95-106G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 1/16 | chr1 | 22569183 | ||||||
chr1:22569452 | C | CCCAGAGA others(48): Show |
1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.159+101_159+155dup others(55): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22569452 | |||||
chr1:22569502 | T | C | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+149T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22569502 | ||||||
chr1:22569505 | T | A | 29 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0103others(26): Show | 30 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.159+152T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22569505 | ||||||
chr1:22569607 | C | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+254C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22569607 | ||||||
chr1:22569608 | A | G | 2 | a0000c0007t0001g0005a0001c0001t0001g0005 | 3 | NA18959.hp2 NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.159+255A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22569608 | ||||||
chr1:22569759 | A | G | 1 | a0001c0002t0006g0217 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.159+406A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22569759 | ||||||
chr1:22569774 | C | T | 1 | a0002c0003t0002g0097 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.159+421C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22569774 | ||||||
chr1:22570001 | C | T | 32 | a0001c0002t0005g0073a0001c0002t0005g0074a0001c0010t0002g0093others(29): Show | 36 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.159+648C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570001 | ||||||
chr1:22570110 | C | T | 1 | a0001c0002t0003g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.159+757C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570110 | ||||||
chr1:22570218 | T | C | 1 | a0001c0002t0005g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.159+865T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570218 | ||||||
chr1:22570228 | G | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+875G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570228 | ||||||
chr1:22570229 | T | C | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+876T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570229 | ||||||
chr1:22570248 | GCACA | G | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+901_159+904del others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570248 | |||||
chr1:22570283 | C | A | 9 | a0001c0001t0002g0070a0001c0011t0038g0069a0002c0004t0011g0061others(6): Show | 11 | HG02055.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.159+930C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570283 | ||||||
chr1:22570283 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.159+930C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570283 | ||||||
chr1:22570287 | T | C | 3 | a0001c0001t0024g0162a0002c0004t0034g0164a0006c0038t0024g0161 | 3 | HG02559.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.159+934T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570287 | ||||||
chr1:22570303 | C | T | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.159+950C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570303 | ||||||
chr1:22570321 | T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0219others(1): Show | 5 | HG01081.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+968T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570321 | ||||||
chr1:22570330 | G | GCA | 174 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(171): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.159+980_159+981dup others(2): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570330 | |||||
chr1:22570341 | T | C | 133 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(130): Show | 144 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.159+988T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570341 | ||||||
chr1:22570361 | C | T | 8 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(5): Show | 8 | HG01243.hp2 HG02896.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+1008C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570361 | ||||||
chr1:22570365 | CGT | C | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1016_159+1017d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570365 | |||||
chr1:22570372 | G | A | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1019G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570372 | ||||||
chr1:22570375 | TAC | T | 4 | a0001c0002t0040g0060a0003c0018t0003g0289a0003c0018t0047g0160others(1): Show | 4 | HG02258.hp1 HG02486.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1029_159+1030d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570375 | |||||
chr1:22570382 | ACG | A | 5 | a0001c0001t0008g0146a0001c0002t0039g0300a0005c0019t0004g0147others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+1039_159+1040d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570382 | |||||
chr1:22570382 | ACGCG | A | 3 | a0001c0001t0001g0204a0001c0016t0006g0203a0001c0016t0006g0205 | 3 | HG00280.hp1 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.159+1037_159+1040d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570382 | |||||
chr1:22570384 | G | A | 1 | a0001c0002t0004g0065 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+1031G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570384 | ||||||
chr1:22570386 | G | A | 4 | a0001c0009t0003g0049a0001c0009t0013g0044a0001c0009t0013g0045others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1033G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570386 | ||||||
chr1:22570389 | C | T | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1036C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570389 | ||||||
chr1:22570391 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.159+1038C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570391 | ||||||
chr1:22570440 | G | GCATACTT others(86): Show |
117 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(114): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.159+1142_159+1143i others(95): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570440 | |||||
chr1:22570496 | A | AATAATAA others(86): Show |
12 | a0001c0001t0008g0146a0001c0002t0002g0149a0001c0002t0002g0150others(9): Show | 13 | HG00642.hp1 HG01109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+1182_159+1183i others(95): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570496 | |||||
chr1:22570496 | A | G | 121 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(118): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.159+1143A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570496 | ||||||
chr1:22570513 | T | TGATGATG others(86): Show |
2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1182_159+1183i others(95): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22570513 | |||||
chr1:22570563 | A | C | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1210A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570563 | ||||||
chr1:22570665 | C | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.159+1312C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570665 | ||||||
chr1:22570677 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.159+1324C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570677 | ||||||
chr1:22570697 | A | C | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.159+1344A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570697 | ||||||
chr1:22570769 | T | C | 33 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.159+1416T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570769 | ||||||
chr1:22570801 | C | T | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159+1448C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570801 | ||||||
chr1:22570901 | G | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1548G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22570901 | ||||||
chr1:22571110 | G | T | 1 | a0000c0007t0003g0197 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.159+1757G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571110 | ||||||
chr1:22571154 | C | T | 1 | a0001c0011t0010g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.159+1801C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571154 | ||||||
chr1:22571236 | A | G | 1 | a0001c0001t0033g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.159+1883A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571236 | ||||||
chr1:22571287 | G | GAACAGGT others(7): Show |
1 | a0001c0001t0001g0198 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.159+1935_159+1948d others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22571287 | |||||
chr1:22571424 | T | C | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.159+2071T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571424 | ||||||
chr1:22571584 | C | T | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159+2231C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571584 | ||||||
chr1:22571614 | T | G | 2 | a0001c0001t0007g0116a0001c0001t0007g0117 | 2 | HG01257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.159+2261T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571614 | ||||||
chr1:22571782 | G | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+2429G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571782 | ||||||
chr1:22571789 | C | T | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+2436C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571789 | ||||||
chr1:22571835 | G | A | 4 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0022g0156others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+2482G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571835 | ||||||
chr1:22571890 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.159+2537A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571890 | ||||||
chr1:22571900 | G | A | 4 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0022g0156others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+2547G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571900 | ||||||
chr1:22571922 | C | A | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+2569C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22571922 | ||||||
chr1:22572201 | G | A | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+2848G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572201 | ||||||
chr1:22572255 | G | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+2902G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572255 | ||||||
chr1:22572259 | G | T | 1 | a0001c0002t0006g0295 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.159+2906G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572259 | ||||||
chr1:22572263 | C | T | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2910C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572263 | ||||||
chr1:22572381 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.159+3028G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572381 | ||||||
chr1:22572448 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.159+3095G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572448 | ||||||
chr1:22572518 | T | C | 178 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(175): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.159+3165T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572518 | ||||||
chr1:22572563 | C | T | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.159+3210C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572563 | ||||||
chr1:22572565 | A | G | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.159+3212A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572565 | ||||||
chr1:22572730 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+3377C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572730 | ||||||
chr1:22572741 | G | A | 1 | a0001c0002t0045g0172 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.159+3388G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572741 | ||||||
chr1:22572954 | G | A | 6 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-3263G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572954 | ||||||
chr1:22572964 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.160-3253A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22572964 | ||||||
chr1:22573021 | G | A | 32 | a0001c0002t0005g0073a0001c0002t0005g0074a0001c0010t0002g0093others(29): Show | 36 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.160-3196G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573021 | ||||||
chr1:22573084 | C | T | 7 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(4): Show | 7 | HG02040.hp1 HG02486.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-3133C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573084 | ||||||
chr1:22573117 | G | A | 34 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(31): Show | 35 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.160-3100G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573117 | ||||||
chr1:22573224 | C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0204a0001c0001t0001g0210others(31): Show | 41 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-2993C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573224 | ||||||
chr1:22573251 | A | G | 41 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(38): Show | 42 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.160-2966A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573251 | ||||||
chr1:22573311 | G | A | 2 | a0001c0002t0007g0173a0001c0002t0045g0172 | 2 | HG01123.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.160-2906G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573311 | ||||||
chr1:22573320 | C | T | 2 | a0001c0001t0003g0276a0011c0025t0003g0278 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.160-2897C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573320 | ||||||
chr1:22573488 | C | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0027g0144 | 3 | HG00597.hp1 NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.160-2729C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573488 | ||||||
chr1:22573548 | GC | G | 5 | a0001c0001t0008g0146a0001c0002t0005g0064a0005c0019t0004g0147others(2): Show | 5 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-2663delC | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22573548 | |||||
chr1:22573554 | CT | C | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.160-2662delT | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573554 | ||||||
chr1:22573556 | C | A | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.160-2661C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573556 | ||||||
chr1:22573653 | C | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.160-2564C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573653 | ||||||
chr1:22573735 | GC | G | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-2480delC | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22573735 | |||||
chr1:22573817 | C | G | 1 | a0002c0004t0034g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160-2400C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22573817 | ||||||
chr1:22574009 | C | T | 2 | a0001c0002t0004g0141a0001c0015t0008g0140 | 2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.160-2208C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574009 | ||||||
chr1:22574139 | C | T | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160-2078C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574139 | ||||||
chr1:22574143 | C | T | 41 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(38): Show | 42 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.160-2074C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574143 | ||||||
chr1:22574149 | T | C | 1 | a0001c0002t0004g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160-2068T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574149 | ||||||
chr1:22574155 | A | G | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-2062A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574155 | ||||||
chr1:22574170 | G | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.160-2047G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574170 | ||||||
chr1:22574271 | GC | G | 7 | a0001c0006t0004g0288a0001c0006t0005g0282a0001c0006t0005g0283others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1943delC | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22574271 | |||||
chr1:22574275 | G | A | 10 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(7): Show | 10 | HG01243.hp2 HG02896.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-1942G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574275 | ||||||
chr1:22574282 | C | T | 1 | a0001c0001t0007g0139 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.160-1935C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574282 | ||||||
chr1:22574535 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.160-1682T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574535 | ||||||
chr1:22574571 | T | C | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-1646T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574571 | ||||||
chr1:22574715 | G | A | 1 | a0002c0040t0009g0030 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.160-1502G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574715 | ||||||
chr1:22574759 | A | G | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160-1458A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574759 | ||||||
chr1:22574848 | C | T | 1 | a0002c0003t0002g0096 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.160-1369C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574848 | ||||||
chr1:22574929 | T | C | 1 | a0002c0004t0014g0003 | 3 | HG02976.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.160-1288T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574929 | ||||||
chr1:22574953 | A | G | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.160-1264A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22574953 | ||||||
chr1:22574959 | A | AT | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-1249dupT | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22574959 | |||||
chr1:22575033 | C | T | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-1184C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575033 | ||||||
chr1:22575100 | G | A | 9 | a0001c0001t0002g0070a0001c0011t0038g0069a0002c0004t0011g0061others(6): Show | 11 | HG02055.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-1117G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575100 | ||||||
chr1:22575125 | A | G | 1 | a0001c0020t0048g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-1092A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575125 | ||||||
chr1:22575147 | C | T | 30 | a0001c0010t0002g0093a0001c0010t0007g0080a0001c0010t0009g0029others(27): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-1070C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575147 | ||||||
chr1:22575221 | G | A | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-996G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575221 | ||||||
chr1:22575250 | CTTATTA | C | 68 | a0000c0007t0010g0158a0001c0001t0002g0070a0001c0001t0010g0168others(65): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.160-961_160-956del others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22575250 | |||||
chr1:22575292 | G | A | 1 | a0001c0015t0008g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.160-925G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575292 | ||||||
chr1:22575376 | C | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.160-841C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575376 | ||||||
chr1:22575415 | T | TGCCCATT others(325): Show |
3 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0017t0008g0304 | 3 | NA18957.hp2 NA19057.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.160-791_160-790ins others(332): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22575415 | |||||
chr1:22575415 | T | TGCCCATT others(326): Show |
1 | a0001c0013t0017g0308 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.160-791_160-790ins others(333): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22575415 | |||||
chr1:22575415 | T | TGCCCATT others(326): Show |
1 | a0001c0017t0008g0305 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.160-791_160-790ins others(333): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 22575415 | |||||
chr1:22575493 | C | T | 3 | a0001c0001t0002g0098a0004c0012t0002g0007a0004c0012t0002g0025 | 4 | HG02145.hp1 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-724C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575493 | ||||||
chr1:22575526 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.160-691C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575526 | ||||||
chr1:22575740 | T | A | 43 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(40): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.160-477T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575740 | ||||||
chr1:22575861 | T | C | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-356T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575861 | ||||||
chr1:22575938 | G | A | 1 | a0001c0001t0025g0157 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.160-279G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22575938 | ||||||
chr1:22576030 | C | T | 7 | a0001c0006t0004g0288a0001c0006t0005g0282a0001c0006t0005g0283others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-187C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22576030 | ||||||
chr1:22576044 | C | T | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160-173C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22576044 | ||||||
chr1:22576072 | G | A | 28 | a0001c0010t0002g0093a0001c0010t0007g0080a0001c0010t0009g0029others(25): Show | 32 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.160-145G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22576072 | ||||||
chr1:22576132 | G | A | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-85G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22576132 | ||||||
chr1:22576142 | C | A | 2 | a0001c0001t0009g0062a0001c0002t0005g0063 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.160-75C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 2/16 | chr1 | 22576142 | ||||||
chr1:22576983 | A | G | 43 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(40): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.823+103A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22576983 | ||||||
chr1:22577120 | C | T | 9 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+240C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577120 | ||||||
chr1:22577126 | G | C | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+246G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577126 | ||||||
chr1:22577178 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.823+298A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577178 | ||||||
chr1:22577195 | C | T | 1 | a0001c0013t0017g0307 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.823+315C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577195 | ||||||
chr1:22577217 | T | C | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+337T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577217 | ||||||
chr1:22577236 | C | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+356C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577236 | ||||||
chr1:22577291 | T | G | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+411T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577291 | ||||||
chr1:22577299 | G | A | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+419G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577299 | ||||||
chr1:22577339 | T | C | 30 | a0001c0010t0002g0093a0001c0010t0007g0080a0001c0010t0009g0029others(27): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+459T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577339 | ||||||
chr1:22577433 | C | T | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+553C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577433 | ||||||
chr1:22577774 | GTGTGTGC others(1): Show |
G | 5 | a0001c0001t0002g0011a0001c0001t0002g0133a0001c0001t0002g0143others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+902_823+909del others(8): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577774 | |||||
chr1:22577806 | A | G | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823+926A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577806 | ||||||
chr1:22577824 | A | G | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823+944A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577824 | ||||||
chr1:22577839 | C | A | 1 | a0017c0036t0002g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.823+959C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577839 | ||||||
chr1:22577849 | T | G | 35 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(32): Show | 36 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+969T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577849 | ||||||
chr1:22577855 | C | CGTGT | 114 | a0000c0007t0035g0006a0000c0041t0001g0031a0000c0042t0003g0106others(111): Show | 125 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(122): Show |
intron_variant | MODIFIER | c.823+977_823+978ins others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577855 | |||||
chr1:22577857 | T | TGTGC | 16 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0007g0173others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.823+977_823+978ins others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577857 | ||||||
chr1:22577861 | T | C | 16 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0007g0173others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.823+981T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577861 | ||||||
chr1:22577883 | T | G | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1003T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577883 | ||||||
chr1:22577888 | A | AGTGTGTG others(79): Show |
1 | a0001c0002t0005g0022 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.823+1019_823+1020i others(88): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577888 | |||||
chr1:22577888 | A | AGTGTGTG others(79): Show |
1 | a0001c0002t0005g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823+1019_823+1020i others(88): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577888 | |||||
chr1:22577902 | T | TGTGTATG others(9): Show |
1 | a0001c0002t0004g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823+1052_823+1067d others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577902 | |||||
chr1:22577904 | T | C | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1024T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577904 | ||||||
chr1:22577906 | T | TGC | 40 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(37): Show | 41 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.823+1026_823+1027i others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577906 | ||||||
chr1:22577914 | C | CAT | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1034_823+1035i others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577914 | ||||||
chr1:22577930 | CGT | C | 11 | a0001c0001t0001g0013a0001c0001t0002g0070a0001c0011t0038g0069others(8): Show | 13 | HG02055.hp2 HG02818.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.823+1052_823+1053d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577930 | |||||
chr1:22577931 | G | A | 42 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(39): Show | 44 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.823+1051G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577931 | ||||||
chr1:22577931 | G | GAGTGTAT others(51): Show |
1 | a0001c0020t0012g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.823+1051_823+1052i others(60): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577931 | ||||||
chr1:22577934 | A | T | 43 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(40): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.823+1054A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577934 | ||||||
chr1:22577937 | GTA | G | 5 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0022g0156others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+1059_823+1060d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577937 | |||||
chr1:22577938 | T | C | 3 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0020t0012g0024 | 4 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1058T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577938 | ||||||
chr1:22577938 | T | TATGCATG others(1242): Show |
1 | a0001c0011t0038g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.823+1061_823+1062i others(1251): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1242): Show |
1 | a0001c0001t0002g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.823+1061_823+1062i others(1251): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1264): Show |
2 | a0001c0001t0001g0013a0012c0029t0001g0013 | 2 | HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1273): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1254): Show |
4 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(1): Show | 6 | HG02976.hp2 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1263): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1252): Show |
2 | a0002c0004t0011g0180a0002c0004t0032g0179 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1261): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1230): Show |
1 | a0002c0004t0011g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.823+1061_823+1062i others(1239): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(77): Show |
2 | a0001c0022t0004g0027a0001c0022t0004g0028 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.823+1061_823+1062i others(86): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1258): Show |
2 | a0001c0021t0012g0104a0001c0021t0012g0105 | 2 | HG01192.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1267): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1260): Show |
19 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(16): Show | 19 | HG00733.hp2 HG00735.hp2 HG03654.hp1 others(16): Show |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1269): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1258): Show |
1 | a0001c0008t0012g0010 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1267): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1262): Show |
2 | a0001c0046t0037g0297a0004c0044t0002g0296 | 2 | HG01106.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1271): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1264): Show |
5 | a0001c0009t0003g0049a0001c0009t0013g0044a0001c0009t0013g0045others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1273): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1270): Show |
2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+1061_823+1062i others(1279): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(1260): Show |
1 | a0002c0043t0002g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823+1061_823+1062i others(1269): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577938 | T | TATGCATG others(59): Show |
5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1061_823+1062i others(68): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577938 | |||||
chr1:22577946 | C | CATCT | 43 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0013others(40): Show | 46 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+1066_823+1067i others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577946 | ||||||
chr1:22577946 | C | CATGTGTG others(3): Show |
2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1066_823+1067i others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577946 | ||||||
chr1:22577948 | A | T | 47 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0013others(44): Show | 50 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.823+1068A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577948 | ||||||
chr1:22577949 | G | A | 1 | a0003c0047t0013g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.823+1069G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577949 | ||||||
chr1:22577949 | G | GAGTGTA | 3 | a0001c0020t0012g0024a0001c0022t0004g0027a0001c0022t0004g0028 | 3 | HG01891.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.823+1069_823+1070i others(8): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577949 | ||||||
chr1:22577949 | G | GTGTA | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1072_823+1075d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577949 | |||||
chr1:22577953 | A | G | 44 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0013others(41): Show | 47 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.823+1073A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577953 | ||||||
chr1:22577957 | ATG | A | 3 | a0000c0007t0001g0218a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02071.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1084_823+1085d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577957 | |||||
chr1:22577958 | T | A | 32 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(29): Show | 33 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.823+1078T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577958 | ||||||
chr1:22577963 | G | A | 1 | a0003c0047t0013g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.823+1083G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577963 | ||||||
chr1:22577966 | C | T | 1 | a0003c0047t0013g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.823+1086C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577966 | ||||||
chr1:22577967 | A | ATG | 43 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0013others(40): Show | 46 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+1090_823+1091d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577967 | |||||
chr1:22577974 | T | C | 1 | a0003c0047t0013g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.823+1094T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577974 | ||||||
chr1:22577979 | G | A | 43 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0013others(40): Show | 46 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+1099G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577979 | ||||||
chr1:22577982 | C | T | 1 | a0001c0002t0007g0173 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.823+1102C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577982 | ||||||
chr1:22577983 | A | G | 1 | a0002c0004t0034g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.823+1103A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577983 | ||||||
chr1:22577987 | G | GCATGTGT others(1288): Show |
1 | a0002c0004t0034g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.823+1107_823+1108i others(1297): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577987 | ||||||
chr1:22577987 | G | GTGTGCAT others(1190): Show |
1 | a0001c0020t0012g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.823+1109_823+1110i others(1199): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577987 | |||||
chr1:22577987 | G | GTGTGCAT others(1271): Show |
1 | a0001c0002t0005g0064 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823+1109_823+1110i others(1280): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577987 | |||||
chr1:22577987 | G | GTGTGCAT others(1289): Show |
3 | a0001c0013t0017g0306a0001c0017t0008g0304a0001c0017t0008g0305 | 3 | HG02040.hp1 NA19057.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.823+1109_823+1110i others(1298): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577987 | |||||
chr1:22577987 | G | GTGTGCAT others(1271): Show |
1 | a0001c0002t0005g0022 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.823+1109_823+1110i others(1280): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577987 | |||||
chr1:22577987 | G | GTGTGCAT others(1184): Show |
2 | a0001c0022t0004g0027a0001c0022t0004g0028 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.823+1109_823+1110i others(1193): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577987 | |||||
chr1:22577990 | C | CATGTGTG others(1258): Show |
2 | a0001c0001t0008g0146a0005c0019t0004g0147 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1267): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1284): Show |
1 | a0001c0016t0006g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1293): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1286): Show |
1 | a0001c0001t0003g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1295): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1288): Show |
1 | a0001c0002t0003g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1297): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1260): Show |
1 | a0005c0019t0004g0148 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1269): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1260): Show |
1 | a0018c0035t0008g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1269): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1286): Show |
3 | a0001c0001t0002g0098a0004c0012t0002g0007a0004c0012t0002g0025 | 4 | HG02145.hp1 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1295): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1288): Show |
1 | a0001c0002t0008g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1297): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0001t0003g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0001c0001t0018g0227 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0001c0001t0001g0228 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0014c0026t0001g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1288): Show |
2 | a0001c0001t0001g0204a0001c0016t0006g0205 | 2 | HG00280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1297): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1258): Show |
1 | a0001c0002t0003g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1267): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0002t0006g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0001t0003g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
2 | a0001c0001t0001g0291a0001c0001t0001g0294 | 2 | NA19010.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
2 | a0001c0001t0003g0276a0011c0025t0003g0278 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
105 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0003g0197others(102): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0199a0001c0001t0001g0219 | 4 | HG02071.hp2 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0001c0002t0006g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0001t0018g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0001t0001g0266 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0001t0001g0279 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1286): Show |
2 | a0001c0001t0005g0268a0001c0002t0005g0267 | 2 | HG01943.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1295): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0001t0007g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1288): Show |
1 | a0001c0001t0001g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1297): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
2 | a0001c0002t0006g0215a0002c0004t0009g0216 | 2 | NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1276): Show |
1 | a0001c0002t0002g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1285): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1278): Show |
2 | a0001c0002t0002g0150a0001c0002t0002g0151 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1287): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1282): Show |
3 | a0001c0002t0002g0152a0001c0002t0002g0153a0001c0002t0002g0154 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1291): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1290): Show |
1 | a0001c0011t0010g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1299): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1294): Show |
1 | a0001c0015t0008g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1303): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1294): Show |
2 | a0001c0001t0007g0135a0001c0001t0007g0136 | 2 | HG00597.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1303): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0001c0001t0009g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1294): Show |
26 | a0001c0001t0002g0011a0001c0001t0002g0133a0001c0001t0002g0143others(23): Show | 27 | HG00438.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1303): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0003c0014t0015g0023 | 2 | HG00642.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0001c0002t0004g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
2 | a0001c0002t0004g0128a0001c0002t0004g0129 | 2 | HG01943.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
1 | a0001c0002t0008g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1288): Show |
6 | a0001c0001t0007g0115a0001c0002t0004g0110a0001c0002t0004g0111others(3): Show | 6 | HG00738.hp2 HG01358.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1297): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
2 | a0001c0002t0004g0141a0001c0015t0008g0140 | 2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1270): Show |
3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1279): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1306): Show |
1 | a0000c0007t0001g0269 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1315): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1292): Show |
2 | a0001c0001t0007g0116a0001c0001t0007g0117 | 2 | HG01257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1301): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1272): Show |
1 | a0002c0003t0002g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1281): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(2977): Show |
1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(2986): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1294): Show |
1 | a0001c0001t0025g0026 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1303): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1284): Show |
5 | a0001c0001t0010g0170a0001c0001t0016g0166a0001c0001t0033g0171others(2): Show | 5 | HG02896.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1293): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1272): Show |
1 | a0002c0003t0002g0008 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1281): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1262): Show |
1 | a0001c0020t0048g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1271): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1274): Show |
1 | a0002c0003t0002g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1283): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1266): Show |
1 | a0002c0003t0002g0077 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1275): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1274): Show |
23 | a0001c0010t0002g0093a0001c0010t0007g0080a0001c0010t0009g0029others(20): Show | 26 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1283): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1274): Show |
1 | a0017c0036t0002g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1283): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1284): Show |
3 | a0001c0001t0010g0168a0001c0001t0016g0167a0001c0001t0016g0169 | 3 | HG01243.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.823+1114_823+1115i others(1293): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1274): Show |
1 | a0001c0002t0004g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1283): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CATGTGTG others(1294): Show |
1 | a0001c0002t0004g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.823+1114_823+1115i others(1303): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577990 | |||||
chr1:22577990 | C | CGTGAATG others(1): Show |
43 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0013others(40): Show | 46 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.823+1110_823+1111i others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGAGTG others(1279): Show |
1 | a0001c0013t0017g0308 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1288): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGAGTG others(1280): Show |
1 | a0001c0013t0017g0307 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1289): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTA others(1284): Show |
2 | a0001c0001t0024g0162a0006c0038t0024g0161 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.823+1110_823+1111i others(1293): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTA others(1260): Show |
1 | a0003c0047t0013g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1269): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1235): Show |
1 | a0000c0007t0010g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1244): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1237): Show |
2 | a0001c0002t0022g0156a0001c0002t0022g0159 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.823+1110_823+1111i others(1246): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1263): Show |
1 | a0001c0006t0005g0282 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1272): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1265): Show |
9 | a0001c0002t0007g0173a0001c0002t0045g0172a0001c0006t0005g0283others(6): Show | 9 | HG00140.hp1 HG00323.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+1110_823+1111i others(1274): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1263): Show |
1 | a0001c0002t0040g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1272): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1255): Show |
1 | a0001c0001t0025g0157 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1264): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1263): Show |
1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1272): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | CGTGTGTG others(1265): Show |
1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.823+1110_823+1111i others(1274): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577990 | C | T | 9 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+1110C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22577990 | ||||||
chr1:22577999 | CTG | C | 9 | a0001c0001t0002g0070a0001c0011t0038g0069a0002c0004t0011g0061others(6): Show | 11 | HG02055.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+1126_823+1127d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22577999 | |||||
chr1:22578033 | GTGTA | G | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1161_823+1164d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578033 | |||||
chr1:22578049 | GTGTGTGC others(1): Show |
G | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1180_823+1187d others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578049 | |||||
chr1:22578079 | ATG | A | 11 | a0000c0007t0010g0158a0001c0001t0001g0015a0001c0001t0001g0199others(8): Show | 13 | HG00642.hp1 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.823+1206_823+1207d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578079 | |||||
chr1:22578080 | T | TGTGTGTG others(12): Show |
25 | a0001c0001t0002g0011a0001c0001t0002g0133a0001c0001t0002g0143others(22): Show | 26 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.823+1205_823+1223d others(21): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578080 | |||||
chr1:22578098 | CAGTGTAT others(13): Show |
C | 21 | a0000c0007t0001g0218a0001c0001t0001g0017a0001c0001t0001g0041others(18): Show | 22 | HG00621.hp2 HG01993.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.823+1236_823+1255d others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578098 | |||||
chr1:22578104 | A | G | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1224A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578104 | ||||||
chr1:22578111 | TG | T | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1232delG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578111 | ||||||
chr1:22578112 | GTGCGTGA others(5): Show |
G | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1236_823+1247d others(14): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578112 | |||||
chr1:22578113 | T | A | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1233T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578113 | ||||||
chr1:22578118 | G | C | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1238G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578118 | ||||||
chr1:22578125 | T | C | 40 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(37): Show | 41 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.823+1245T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578125 | ||||||
chr1:22578127 | CATGTGTG others(9): Show |
C | 2 | a0000c0007t0001g0005a0001c0001t0001g0005 | 3 | NA18959.hp2 NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.823+1256_823+1271d others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578127 | |||||
chr1:22578135 | C | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1255C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578135 | ||||||
chr1:22578136 | A | G | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1256A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578136 | ||||||
chr1:22578136 | ATGTG | A | 37 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(34): Show | 39 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.823+1260_823+1263d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578136 | |||||
chr1:22578139 | T | A | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1259T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578139 | ||||||
chr1:22578140 | GTGTA | G | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1264_823+1267d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578140 | |||||
chr1:22578143 | T | C | 2 | a0001c0002t0002g0152a0001c0002t0002g0153 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.823+1263T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578143 | ||||||
chr1:22578143 | T | TATGC | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1266_823+1267i others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578143 | |||||
chr1:22578147 | T | C | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1267T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578147 | ||||||
chr1:22578151 | C | A | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1271C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578151 | ||||||
chr1:22578151 | C | CGTGA | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1274_823+1275i others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578151 | |||||
chr1:22578152 | G | A | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1272G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578152 | ||||||
chr1:22578159 | C | T | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1279C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578159 | ||||||
chr1:22578163 | A | T | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1283A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578163 | ||||||
chr1:22578163 | AGTGTATG others(9): Show |
A | 25 | a0001c0001t0002g0011a0001c0001t0002g0133a0001c0001t0002g0143others(22): Show | 26 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.823+1288_823+1303d others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578163 | |||||
chr1:22578163 | AGTGTATG others(11): Show |
A | 1 | a0001c0002t0008g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.823+1287_823+1304d others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578163 | |||||
chr1:22578167 | T | C | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1287T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578167 | ||||||
chr1:22578168 | A | G | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1288A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578168 | ||||||
chr1:22578179 | T | A | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+1299T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578179 | ||||||
chr1:22578179 | T | C | 7 | a0001c0006t0004g0288a0001c0006t0005g0282a0001c0006t0005g0283others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+1299T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578179 | ||||||
chr1:22578182 | G | A | 78 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(75): Show | 83 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.823+1302G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578182 | ||||||
chr1:22578185 | C | T | 78 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(75): Show | 83 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.823+1305C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578185 | ||||||
chr1:22578190 | A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0226 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.823+1310A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578190 | ||||||
chr1:22578191 | T | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0226 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.823+1311T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578191 | ||||||
chr1:22578191 | TGTGTGTG others(5): Show |
T | 35 | a0001c0002t0007g0173a0001c0002t0045g0172a0001c0010t0002g0093others(32): Show | 39 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.823+1313_823+1324d others(14): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578191 | |||||
chr1:22578191 | TGTGTGTG others(7): Show |
T | 9 | a0000c0007t0001g0269a0001c0001t0001g0015a0001c0001t0001g0198others(6): Show | 10 | HG01081.hp2 HG01109.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+1323_823+1336d others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578191 | |||||
chr1:22578193 | T | A | 2 | a0001c0001t0024g0162a0006c0038t0024g0161 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.823+1313T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578193 | ||||||
chr1:22578203 | C | CAT | 81 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(78): Show | 87 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.823+1323_823+1324i others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578203 | ||||||
chr1:22578204 | G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG02074.hp2 HG02129.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+1324G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578204 | ||||||
chr1:22578204 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.823+1324G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578204 | ||||||
chr1:22578205 | A | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG02074.hp2 HG02129.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+1325A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578205 | ||||||
chr1:22578207 | T | A | 2 | a0001c0009t0013g0044a0001c0011t0038g0069 | 2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+1327T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578207 | ||||||
chr1:22578213 | CGTGT | C | 18 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0007g0173others(15): Show | 18 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.823+1335_823+1338d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578213 | |||||
chr1:22578214 | G | A | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1334G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578214 | ||||||
chr1:22578217 | T | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG02074.hp2 HG02129.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+1337T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578217 | ||||||
chr1:22578219 | A | AGTGTGCA others(9): Show |
4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1354_823+1369d others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578219 | |||||
chr1:22578219 | AGT | A | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1343_823+1344d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578219 | |||||
chr1:22578219 | AGTGTGCA others(1): Show |
A | 6 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1345_823+1352d others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578219 | |||||
chr1:22578226 | ATG | A | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1352_823+1353d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578226 | |||||
chr1:22578226 | ATGTG | A | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.823+1350_823+1353d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578226 | |||||
chr1:22578242 | ATG | A | 16 | a0001c0001t0001g0202a0001c0001t0007g0108a0001c0001t0007g0115others(13): Show | 16 | HG00323.hp2 HG00438.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.823+1370_823+1371d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578242 | |||||
chr1:22578242 | ATGTG | A | 42 | a0000c0007t0035g0006a0000c0041t0001g0031a0000c0042t0003g0106others(39): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.823+1368_823+1371d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578242 | |||||
chr1:22578353 | T | C | 1 | a0001c0002t0008g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.823+1473T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578353 | ||||||
chr1:22578358 | G | A | 6 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1478G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578358 | ||||||
chr1:22578364 | G | A | 39 | a0000c0007t0010g0158a0001c0001t0002g0070a0001c0001t0010g0168others(36): Show | 41 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.823+1484G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578364 | ||||||
chr1:22578369 | C | T | 33 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+1489C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578369 | ||||||
chr1:22578382 | ATGTATGC others(13): Show |
A | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1521_823+1540d others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578382 | |||||
chr1:22578386 | A | C | 6 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1506A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578386 | ||||||
chr1:22578390 | A | G | 1 | a0001c0033t0006g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.823+1510A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578390 | ||||||
chr1:22578394 | C | G | 112 | a0000c0007t0010g0158a0000c0041t0001g0031a0000c0042t0003g0106others(109): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.823+1514C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578394 | ||||||
chr1:22578413 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.823+1533T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578413 | ||||||
chr1:22578436 | GTGTGTGC others(1): Show |
G | 21 | a0001c0001t0002g0070a0001c0001t0010g0168a0001c0001t0010g0170others(18): Show | 23 | HG01243.hp2 HG02055.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.823+1564_823+1571d others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578436 | |||||
chr1:22578472 | ATGTGCAT others(13): Show |
A | 1 | a0001c0006t0005g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.823+1605_823+1624d others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578472 | |||||
chr1:22578489 | C | T | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.823+1609C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578489 | ||||||
chr1:22578512 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+1632G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578512 | ||||||
chr1:22578528 | CAT | C | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1651_823+1652d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578528 | |||||
chr1:22578534 | C | T | 33 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+1654C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578534 | ||||||
chr1:22578547 | G | A | 33 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+1667G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578547 | ||||||
chr1:22578561 | T | TTG | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1683_823+1684d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578561 | |||||
chr1:22578571 | CTGCATGT others(9): Show |
C | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1695_823+1710d others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578571 | |||||
chr1:22578623 | G | A | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1743G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578623 | ||||||
chr1:22578626 | TGTGC | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1747_823+1750d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578626 | ||||||
chr1:22578630 | C | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1750C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578630 | ||||||
chr1:22578635 | GTGTA | G | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+1759_823+1762d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578635 | |||||
chr1:22578643 | G | GTGTT | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1764_823+1765i others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578643 | |||||
chr1:22578645 | ATG | A | 44 | a0000c0007t0010g0158a0001c0001t0002g0070a0001c0001t0010g0168others(41): Show | 46 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.823+1772_823+1773d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578645 | |||||
chr1:22578654 | C | A | 30 | a0001c0010t0002g0093a0001c0010t0007g0080a0001c0010t0009g0029others(27): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+1774C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578654 | ||||||
chr1:22578658 | TGA | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+1780_823+1781d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578658 | |||||
chr1:22578697 | C | CTG | 43 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0008g0006others(40): Show | 48 | HG00140.hp2 HG00642.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.823+1825_823+1826d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578697 | |||||
chr1:22578697 | C | CTGTG | 42 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(39): Show | 44 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.823+1823_823+1826d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578697 | |||||
chr1:22578697 | CTG | C | 27 | a0000c0007t0010g0158a0001c0001t0002g0070a0001c0001t0010g0168others(24): Show | 31 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.823+1825_823+1826d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578697 | |||||
chr1:22578697 | CTGTG | C | 14 | a0001c0002t0004g0110a0001c0002t0007g0173a0001c0002t0040g0060others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.823+1823_823+1826d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578697 | |||||
chr1:22578723 | G | A | 1 | a0001c0002t0026g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.823+1843G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578723 | ||||||
chr1:22578755 | ATG | A | 43 | a0001c0001t0002g0011a0001c0001t0002g0133a0001c0001t0002g0143others(40): Show | 44 | HG00438.hp2 HG00597.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.823+1882_823+1883d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578755 | |||||
chr1:22578776 | C | T | 1 | a0001c0002t0004g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.823+1896C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578776 | ||||||
chr1:22578782 | G | T | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+1902G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578782 | ||||||
chr1:22578792 | T | A | 3 | a0000c0041t0001g0031a0001c0005t0003g0032a0009c0039t0003g0310 | 3 | NA18975.hp1 NA18985.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.823+1912T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578792 | ||||||
chr1:22578798 | C | T | 2 | a0002c0004t0011g0061a0002c0004t0011g0178 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.823+1918C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578798 | ||||||
chr1:22578825 | A | G | 42 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(39): Show | 44 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.823+1945A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578825 | ||||||
chr1:22578855 | A | C | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1975A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578855 | ||||||
chr1:22578863 | A | G | 6 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+1983A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578863 | ||||||
chr1:22578869 | ACGTGTCC others(1): Show |
A | 20 | a0001c0001t0002g0070a0001c0001t0010g0168a0001c0001t0010g0170others(17): Show | 22 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(19): Show |
intron_variant | MODIFIER | c.823+1990_823+1997d others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578869 | ||||||
chr1:22578870 | C | T | 108 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(105): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.823+1990C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578870 | ||||||
chr1:22578875 | C | G | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1995C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578875 | ||||||
chr1:22578876 | C | CATGCATG others(9): Show |
3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1996_823+1997i others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578876 | ||||||
chr1:22578876 | C | CGT | 42 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(39): Show | 44 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.823+2001_823+2002d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578876 | |||||
chr1:22578878 | T | C | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1998T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578878 | ||||||
chr1:22578901 | ATGTG | A | 33 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301others(30): Show | 38 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.823+2023_823+2026d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578901 | |||||
chr1:22578923 | T | G | 117 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(114): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.823+2043T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578923 | ||||||
chr1:22578925 | A | G | 1 | a0001c0017t0008g0304 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.823+2045A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578925 | ||||||
chr1:22578929 | G | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+2049G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578929 | ||||||
chr1:22578937 | GTGTATGT others(111): Show |
G | 17 | a0001c0001t0007g0108a0001c0001t0007g0115a0001c0001t0007g0116others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+2077_823+2194d others(2): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578937 | |||||
chr1:22578949 | ATG | A | 30 | a0001c0010t0002g0093a0001c0010t0007g0080a0001c0010t0009g0029others(27): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+2075_823+2076d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22578949 | |||||
chr1:22578957 | C | A | 115 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(112): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.823+2077C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578957 | ||||||
chr1:22578976 | T | C | 130 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(127): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.823+2096T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578976 | ||||||
chr1:22578993 | A | G | 4 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0022g0156others(1): Show | 4 | HG00735.hp1 HG01106.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+2113A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22578993 | ||||||
chr1:22579005 | ATG | A | 22 | a0001c0001t0002g0070a0001c0001t0010g0168a0001c0001t0010g0170others(19): Show | 24 | HG01243.hp2 HG02055.hp2 HG02602.hp1 others(21): Show |
intron_variant | MODIFIER | c.823+2132_823+2133d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579005 | |||||
chr1:22579015 | A | G | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823+2135A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579015 | ||||||
chr1:22579030 | TG | T | 33 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+2151delG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579030 | ||||||
chr1:22579037 | ATG | A | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+2164_823+2165d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579037 | |||||
chr1:22579055 | A | ATGTG | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+2178_823+2179i others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579055 | |||||
chr1:22579059 | A | T | 4 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(1): Show | 4 | HG02451.hp1 HG02723.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+2179A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579059 | ||||||
chr1:22579059 | ATGTATGC others(3): Show |
A | 1 | a0018c0035t0008g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.823+2183_823+2192d others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579059 | |||||
chr1:22579069 | GTGTGTGC others(13): Show |
G | 32 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(29): Show | 33 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.823+2204_823+2223d others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579069 | |||||
chr1:22579078 | T | C | 2 | a0001c0001t0024g0162a0006c0038t0024g0161 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.823+2198T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579078 | ||||||
chr1:22579083 | A | G | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+2203A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579083 | ||||||
chr1:22579084 | CGTGCATG others(15): Show |
C | 38 | a0000c0007t0010g0158a0001c0001t0002g0070a0001c0001t0010g0168others(35): Show | 40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.823+2215_823+2236d others(24): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579084 | |||||
chr1:22579095 | GCATGTGT others(15): Show |
G | 1 | a0001c0001t0033g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823+2217_823+2238d others(24): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579095 | |||||
chr1:22579098 | T | G | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+2218T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579098 | ||||||
chr1:22579098 | TGTGTATG others(13): Show |
T | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+2237_823+2256d others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579098 | |||||
chr1:22579103 | ATGTGTGC others(19): Show |
A | 1 | a0001c0045t0019g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.823+2224_823+2249d others(28): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579103 | ||||||
chr1:22579108 | T | G | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+2228T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579108 | ||||||
chr1:22579111 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.823+2231A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579111 | ||||||
chr1:22579128 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.823+2248T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579128 | ||||||
chr1:22579131 | A | ATG | 22 | a0000c0007t0010g0158a0000c0007t0035g0006a0001c0001t0008g0006others(19): Show | 23 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+2260_823+2261d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579131 | |||||
chr1:22579131 | ATG | A | 10 | a0001c0001t0002g0070a0001c0001t0025g0026a0001c0011t0038g0069others(7): Show | 12 | HG02055.hp2 HG02818.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.823+2260_823+2261d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579131 | |||||
chr1:22579142 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+2262C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579142 | ||||||
chr1:22579145 | A | G | 7 | a0001c0006t0004g0288a0001c0006t0005g0282a0001c0006t0005g0283others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+2265A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579145 | ||||||
chr1:22579148 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.823+2268T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579148 | ||||||
chr1:22579159 | ATGTATGC others(3): Show |
A | 1 | a0002c0003t0002g0077 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.823+2283_823+2292d others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579159 | |||||
chr1:22579167 | ATG | A | 30 | a0001c0001t0001g0242a0001c0010t0002g0093a0001c0010t0007g0080others(27): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+2294_823+2295d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579167 | |||||
chr1:22579185 | G | T | 33 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+2305G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579185 | ||||||
chr1:22579186 | T | C | 1 | a0001c0002t0040g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.823+2306T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579186 | ||||||
chr1:22579188 | AAT | A | 3 | a0001c0010t0002g0093a0001c0010t0009g0029a0001c0010t0042g0094 | 3 | NA18965.hp1 NA19063.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.823+2313_823+2314d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579188 | |||||
chr1:22579209 | A | ATG | 39 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(36): Show | 40 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.823+2337_823+2338d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579209 | |||||
chr1:22579209 | ATG | A | 3 | a0001c0002t0004g0221a0001c0002t0006g0214a0003c0018t0047g0160 | 3 | HG02735.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.823+2337_823+2338d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579209 | |||||
chr1:22579219 | A | G | 1 | a0002c0003t0002g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.823+2339A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579219 | ||||||
chr1:22579226 | CAT | C | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+2347_823+2348d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579226 | ||||||
chr1:22579230 | T | C | 35 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(32): Show | 36 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+2350T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579230 | ||||||
chr1:22579342 | AGT | A | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+2465_823+2466d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579342 | |||||
chr1:22579354 | C | CGT | 91 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(88): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.823+2481_823+2482d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579354 | |||||
chr1:22579359 | GTGTA | G | 10 | a0001c0001t0002g0070a0001c0001t0025g0026a0001c0011t0038g0069others(7): Show | 12 | HG02055.hp2 HG02818.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.823+2483_823+2486d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579359 | |||||
chr1:22579361 | GTA | G | 12 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(9): Show | 12 | HG01243.hp2 HG02559.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.823+2483_823+2484d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579361 | |||||
chr1:22579408 | GTGTA | G | 36 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0200others(33): Show | 37 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.823+2536_823+2539d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579408 | |||||
chr1:22579503 | G | A | 1 | a0001c0002t0002g0154 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.823+2623G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579503 | ||||||
chr1:22579522 | G | A | 4 | a0001c0001t0003g0018a0001c0001t0003g0245a0001c0027t0003g0244others(1): Show | 5 | HG01433.hp2 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+2642G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579522 | ||||||
chr1:22579604 | C | T | 1 | a0004c0012t0002g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.823+2724C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579604 | ||||||
chr1:22579657 | G | C | 1 | a0001c0016t0006g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.823+2777G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579657 | ||||||
chr1:22579754 | A | C | 131 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(128): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.823+2874A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579754 | ||||||
chr1:22579761 | G | A | 3 | a0000c0007t0010g0158a0001c0002t0022g0156a0001c0002t0022g0159 | 3 | HG00735.hp1 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.823+2881G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579761 | ||||||
chr1:22579794 | C | G | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+2914C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579794 | ||||||
chr1:22579900 | G | A | 35 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(32): Show | 36 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+3020G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579900 | ||||||
chr1:22579911 | C | T | 1 | a0001c0006t0005g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.823+3031C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22579911 | ||||||
chr1:22579914 | T | TCCCTCTA | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+3037_823+3038i others(9): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22579914 | |||||
chr1:22580017 | G | C | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+3137G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580017 | ||||||
chr1:22580041 | C | G | 8 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(5): Show | 8 | HG01243.hp2 HG02896.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+3161C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580041 | ||||||
chr1:22580118 | T | C | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+3238T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580118 | ||||||
chr1:22580127 | C | CT | 23 | a0001c0001t0002g0143a0001c0001t0003g0186a0001c0001t0003g0196others(20): Show | 23 | HG01175.hp2 HG01358.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+3274dupT | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | C | CTT | 6 | a0000c0007t0003g0197a0001c0001t0003g0275a0001c0001t0003g0299others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+3273_823+3274d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CT | C | 22 | a0001c0001t0003g0272a0001c0001t0010g0168a0001c0001t0010g0170others(19): Show | 23 | HG00323.hp1 HG00642.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+3274delT | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTT | C | 15 | a0001c0001t0002g0070a0001c0001t0024g0162a0001c0002t0010g0165others(12): Show | 17 | HG01928.hp1 HG02027.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+3273_823+3274d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTT | C | 26 | a0000c0007t0035g0006a0001c0001t0007g0138a0001c0001t0008g0006others(23): Show | 31 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.823+3272_823+3274d others(5): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTT | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0198others(6): Show | 10 | HG01081.hp2 HG02071.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+3269_823+3274d others(8): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTTT | C | 73 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0001g0269others(70): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.823+3268_823+3274d others(9): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0242others(6): Show | 9 | HG02630.hp1 HG03516.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+3267_823+3274d others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTTT others(3): Show |
C | 3 | a0001c0002t0002g0152a0002c0004t0011g0061a0002c0037t0002g0078 | 3 | HG01361.hp1 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.823+3265_823+3274d others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTTT others(4): Show |
C | 38 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0002g0098others(35): Show | 40 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.823+3264_823+3274d others(13): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTTT others(6): Show |
C | 1 | a0001c0033t0006g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.823+3262_823+3274d others(15): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.823+3261_823+3274d others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580127 | CTTTTTTT others(11): Show |
C | 1 | a0001c0020t0048g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823+3257_823+3274d others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22580127 | |||||
chr1:22580130 | T | C | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.823+3250T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580130 | ||||||
chr1:22580136 | T | C | 6 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(3): Show | 7 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+3256T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580136 | ||||||
chr1:22580137 | T | C | 1 | a0001c0017t0008g0304 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.823+3257T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580137 | ||||||
chr1:22580161 | G | C | 1 | a0001c0001t0016g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.823+3281G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580161 | ||||||
chr1:22580213 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.823+3333C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580213 | ||||||
chr1:22580288 | G | A | 33 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+3408G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580288 | ||||||
chr1:22580435 | A | G | 7 | a0001c0002t0005g0022a0001c0002t0005g0064a0001c0013t0017g0306others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+3555A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580435 | ||||||
chr1:22580473 | A | G | 1 | a0001c0001t0027g0144 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.823+3593A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580473 | ||||||
chr1:22580607 | A | T | 1 | a0001c0002t0008g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.823+3727A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580607 | ||||||
chr1:22580683 | A | C | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+3803A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580683 | ||||||
chr1:22580729 | C | T | 3 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301 | 4 | HG01099.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+3849C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580729 | ||||||
chr1:22580893 | A | G | 42 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0002t0005g0022others(39): Show | 44 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.823+4013A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580893 | ||||||
chr1:22580906 | C | T | 1 | a0001c0001t0007g0136 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.823+4026C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580906 | ||||||
chr1:22580989 | A | G | 298 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0001g0269others(295): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.823+4109A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22580989 | ||||||
chr1:22581025 | A | G | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+4145A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581025 | ||||||
chr1:22581062 | G | A | 2 | a0003c0018t0003g0289a0003c0018t0047g0160 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+4182G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581062 | ||||||
chr1:22581149 | A | G | 1 | a0002c0004t0034g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.823+4269A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581149 | ||||||
chr1:22581221 | C | T | 1 | a0001c0001t0005g0268 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.823+4341C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581221 | ||||||
chr1:22581346 | G | A | 13 | a0001c0001t0010g0168a0001c0001t0010g0170a0001c0001t0016g0166others(10): Show | 13 | HG01243.hp2 HG02559.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.823+4466G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581346 | ||||||
chr1:22581350 | A | G | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+4470A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581350 | ||||||
chr1:22581378 | G | A | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0281 | 3 | HG02004.hp1 HG04184.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.823+4498G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581378 | ||||||
chr1:22581388 | A | G | 3 | a0003c0014t0015g0023a0003c0014t0015g0302a0008c0034t0002g0176 | 4 | HG00642.hp1 HG02486.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+4508A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581388 | ||||||
chr1:22581417 | A | G | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.823+4537A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581417 | ||||||
chr1:22581574 | G | T | 1 | a0001c0008t0006g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.823+4694G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581574 | ||||||
chr1:22581610 | T | C | 1 | a0001c0002t0004g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.823+4730T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581610 | ||||||
chr1:22581648 | C | T | 1 | a0001c0005t0049g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.823+4768C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581648 | ||||||
chr1:22581792 | T | A | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-4688T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581792 | ||||||
chr1:22581864 | ACAAGGAA others(15): Show |
A | 1 | a0001c0001t0001g0231 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.824-4614_824-4593d others(24): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22581864 | |||||
chr1:22581936 | G | A | 1 | a0001c0002t0003g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.824-4544G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22581936 | ||||||
chr1:22582039 | C | T | 7 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-4441C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582039 | ||||||
chr1:22582057 | C | T | 22 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301others(19): Show | 23 | HG01099.hp2 HG01243.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-4423C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582057 | ||||||
chr1:22582162 | C | T | 1 | a0002c0040t0009g0030 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.824-4318C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582162 | ||||||
chr1:22582187 | G | A | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.824-4293G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582187 | ||||||
chr1:22582205 | A | G | 6 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0008g0006others(3): Show | 8 | HG01099.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-4275A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582205 | ||||||
chr1:22582221 | C | T | 50 | a0000c0007t0010g0158a0000c0041t0001g0031a0000c0042t0003g0106others(47): Show | 52 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.824-4259C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582221 | ||||||
chr1:22582228 | G | A | 131 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(128): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-4252G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582228 | ||||||
chr1:22582370 | C | T | 1 | a0001c0001t0007g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.824-4110C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582370 | ||||||
chr1:22582525 | CA | C | 131 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(128): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-3953delA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22582525 | |||||
chr1:22582577 | A | C | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-3903A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582577 | ||||||
chr1:22582590 | A | T | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-3890A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582590 | ||||||
chr1:22582750 | G | A | 1 | a0001c0011t0038g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.824-3730G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582750 | ||||||
chr1:22582762 | A | G | 1 | a0001c0001t0008g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-3718A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582762 | ||||||
chr1:22582816 | G | A | 1 | a0000c0041t0001g0031 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.824-3664G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582816 | ||||||
chr1:22582898 | A | G | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-3582A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582898 | ||||||
chr1:22582926 | G | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.824-3554G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582926 | ||||||
chr1:22582968 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.824-3512T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582968 | ||||||
chr1:22582986 | T | A | 1 | a0001c0006t0005g0207 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.824-3494T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22582986 | ||||||
chr1:22583111 | G | T | 1 | a0001c0005t0003g0038 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.824-3369G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583111 | ||||||
chr1:22583146 | G | A | 3 | a0001c0001t0002g0098a0004c0012t0002g0007a0004c0012t0002g0025 | 4 | HG02145.hp1 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-3334G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583146 | ||||||
chr1:22583148 | G | A | 3 | a0001c0046t0037g0297a0002c0043t0002g0298a0004c0044t0002g0296 | 3 | HG01106.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.824-3332G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583148 | ||||||
chr1:22583152 | C | T | 4 | a0001c0002t0007g0173a0001c0002t0045g0172a0002c0004t0041g0174others(1): Show | 4 | HG01123.hp1 HG03098.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-3328C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583152 | ||||||
chr1:22583224 | A | G | 131 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(128): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-3256A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583224 | ||||||
chr1:22583277 | C | T | 1 | a0001c0001t0024g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.824-3203C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583277 | ||||||
chr1:22583313 | T | C | 4 | a0001c0001t0008g0146a0005c0019t0004g0147a0005c0019t0004g0148others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-3167T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583313 | ||||||
chr1:22583376 | C | T | 15 | a0000c0007t0010g0158a0001c0001t0025g0157a0001c0002t0007g0173others(12): Show | 15 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.824-3104C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583376 | ||||||
chr1:22583387 | G | A | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-3093G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583387 | ||||||
chr1:22583682 | T | C | 72 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(69): Show | 75 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.824-2798T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583682 | ||||||
chr1:22583712 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-2768C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583712 | ||||||
chr1:22583733 | C | A | 52 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0008g0146others(49): Show | 54 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.824-2747C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583733 | ||||||
chr1:22583947 | C | T | 9 | a0001c0001t0003g0021a0001c0001t0003g0051a0001c0001t0003g0270others(6): Show | 10 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-2533C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583947 | ||||||
chr1:22583958 | C | G | 1 | a0001c0011t0010g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.824-2522C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22583958 | ||||||
chr1:22584042 | G | C | 1 | a0001c0002t0040g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.824-2438G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584042 | ||||||
chr1:22584061 | G | A | 2 | a0001c0001t0002g0143a0001c0002t0039g0300 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.824-2419G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584061 | ||||||
chr1:22584255 | C | T | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.824-2225C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584255 | ||||||
chr1:22584256 | G | A | 2 | a0001c0020t0012g0024a0001c0020t0048g0095 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.824-2224G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584256 | ||||||
chr1:22584315 | G | T | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.824-2165G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584315 | ||||||
chr1:22584316 | C | A | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.824-2164C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584316 | ||||||
chr1:22584544 | G | A | 1 | a0001c0002t0004g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.824-1936G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584544 | ||||||
chr1:22584548 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1932C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584548 | ||||||
chr1:22584549 | G | A | 1 | a0002c0003t0002g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.824-1931G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584549 | ||||||
chr1:22584608 | C | A | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.824-1872C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584608 | ||||||
chr1:22584670 | A | G | 126 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(123): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.824-1810A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584670 | ||||||
chr1:22584702 | T | C | 28 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(25): Show | 29 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.824-1778T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584702 | ||||||
chr1:22584734 | C | T | 6 | a0001c0001t0025g0157a0001c0013t0017g0306a0001c0013t0017g0307others(3): Show | 6 | HG01106.hp2 HG02040.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-1746C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584734 | ||||||
chr1:22584865 | T | C | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.824-1615T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584865 | ||||||
chr1:22584885 | G | A | 117 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(114): Show | 128 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.824-1595G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584885 | ||||||
chr1:22584994 | G | A | 2 | a0001c0002t0006g0208a0001c0002t0006g0215 | 2 | HG00639.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.824-1486G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22584994 | ||||||
chr1:22585023 | T | TTC | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1453_824-1452d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585023 | |||||
chr1:22585027 | C | CTG | 4 | a0001c0001t0001g0256a0001c0006t0005g0207a0001c0006t0005g0212others(1): Show | 4 | HG01074.hp1 HG01169.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1430_824-1429d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585027 | |||||
chr1:22585027 | C | CTGTG | 3 | a0001c0002t0003g0280a0004c0012t0002g0007a0004c0012t0002g0025 | 4 | HG02145.hp1 HG02257.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1432_824-1429d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585027 | |||||
chr1:22585027 | C | CTGTGTGT others(3): Show |
1 | a0001c0002t0026g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.824-1438_824-1429d others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585027 | |||||
chr1:22585027 | C | CTGTGTGT others(5): Show |
2 | a0001c0002t0002g0151a0001c0002t0039g0300 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.824-1440_824-1429d others(14): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585027 | |||||
chr1:22585027 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0234 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.824-1448_824-1429d others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585027 | |||||
chr1:22585042 | T | C | 1 | a0001c0009t0013g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.824-1438T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585042 | ||||||
chr1:22585046 | T | C | 1 | a0001c0009t0013g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.824-1434T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585046 | ||||||
chr1:22585048 | T | C | 2 | a0001c0009t0013g0045a0001c0045t0019g0047 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.824-1432T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585048 | ||||||
chr1:22585048 | T | TGC | 3 | a0001c0001t0002g0011a0001c0001t0002g0133a0001c0001t0002g0143 | 4 | HG01069.hp2 HG01071.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1431_824-1430i others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585048 | |||||
chr1:22585050 | T | C | 11 | a0001c0001t0002g0011a0001c0001t0002g0133a0001c0001t0002g0143others(8): Show | 12 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.824-1430T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585050 | ||||||
chr1:22585050 | T | TGC | 33 | a0001c0001t0001g0222a0001c0001t0001g0255a0001c0001t0007g0108others(30): Show | 33 | HG00438.hp2 HG00597.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.824-1427_824-1426d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGCGCG others(11): Show |
1 | a0001c0022t0004g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.824-1429_824-1428i others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGCG others(1): Show |
14 | a0000c0007t0035g0006a0001c0001t0003g0021a0001c0001t0003g0051others(11): Show | 16 | HG01099.hp2 HG01884.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGCG others(7): Show |
4 | a0001c0001t0025g0026a0001c0046t0037g0297a0002c0043t0002g0298others(1): Show | 4 | HG01106.hp1 HG01109.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(3): Show |
6 | a0001c0001t0003g0275a0001c0001t0025g0157a0001c0002t0002g0012others(3): Show | 6 | HG01106.hp2 HG01123.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(7): Show |
1 | a0001c0020t0048g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.824-1429_824-1428i others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(9): Show |
16 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(13): Show | 17 | HG00733.hp2 HG01192.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(11): Show |
1 | a0001c0005t0003g0033 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.824-1429_824-1428i others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(13): Show |
2 | a0001c0001t0002g0098a0001c0022t0004g0028 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.824-1429_824-1428i others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(3): Show |
9 | a0001c0001t0009g0062a0001c0002t0002g0149a0001c0002t0002g0150others(6): Show | 9 | HG02280.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0009g0132a0001c0002t0040g0060a0001c0011t0008g0134 | 3 | HG01884.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.824-1429_824-1428i others(14): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(7): Show |
9 | a0001c0002t0004g0127a0001c0006t0004g0288a0001c0006t0005g0282others(6): Show | 9 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(9): Show |
8 | a0001c0001t0010g0170a0001c0001t0016g0166a0001c0001t0016g0167others(5): Show | 8 | HG01243.hp2 HG02809.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(11): Show |
4 | a0001c0005t0003g0036a0001c0005t0003g0037a0001c0005t0020g0042others(1): Show | 4 | HG00735.hp2 NA18980.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(5): Show |
3 | a0000c0007t0010g0158a0001c0002t0002g0152a0001c0002t0022g0156 | 3 | HG00735.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.824-1429_824-1428i others(14): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(7): Show |
5 | a0001c0001t0002g0070a0001c0011t0038g0069a0002c0004t0041g0174others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(9): Show |
2 | a0002c0004t0009g0287a0010c0024t0046g0175 | 2 | NA21309.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.824-1429_824-1428i others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(11): Show |
1 | a0001c0002t0004g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.824-1429_824-1428i others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(11): Show |
6 | a0001c0001t0009g0257a0001c0010t0007g0080a0002c0003t0002g0002others(3): Show | 8 | HG00642.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(15): Show |
2 | a0002c0004t0011g0178a0002c0004t0034g0164 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.824-1429_824-1428i others(24): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(11): Show |
1 | a0001c0002t0004g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.824-1429_824-1428i others(20): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(13): Show |
3 | a0001c0001t0007g0138a0002c0003t0002g0091a0003c0014t0015g0302 | 3 | HG02027.hp1 HG02027.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.824-1429_824-1428i others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(15): Show |
1 | a0002c0003t0031g0081 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.824-1429_824-1428i others(24): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(17): Show |
4 | a0002c0004t0011g0061a0002c0004t0011g0181a0002c0004t0014g0003others(1): Show | 6 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(26): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(15): Show |
2 | a0002c0003t0002g0008a0003c0014t0015g0023 | 4 | HG00642.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(24): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(19): Show |
1 | a0002c0004t0011g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.824-1429_824-1428i others(28): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(17): Show |
15 | a0001c0010t0002g0093a0001c0010t0009g0029a0002c0003t0002g0009others(12): Show | 16 | HG00140.hp2 HG01074.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(26): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(19): Show |
4 | a0001c0010t0042g0094a0002c0003t0002g0075a0002c0003t0002g0076others(1): Show | 4 | HG04115.hp2 NA18965.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1429_824-1428i others(28): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585050 | T | TGTGTGTG others(21): Show |
1 | a0002c0003t0002g0090 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.824-1429_824-1428i others(30): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585050 | |||||
chr1:22585052 | C | CGCGCGCG others(3): Show |
1 | a0005c0019t0004g0148 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.824-1426_824-1425i others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585052 | |||||
chr1:22585052 | C | CGCGCGCG others(9): Show |
4 | a0001c0009t0003g0049a0001c0009t0013g0044a0001c0009t0013g0046others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1426_824-1425i others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585052 | |||||
chr1:22585052 | C | CGCGCGCT others(3): Show |
1 | a0001c0005t0028g0052 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.824-1426_824-1425i others(12): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585052 | |||||
chr1:22585052 | C | CGCGCGTG others(7): Show |
1 | a0001c0045t0019g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.824-1426_824-1425i others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585052 | |||||
chr1:22585052 | C | T | 117 | a0000c0007t0035g0006a0000c0041t0001g0031a0000c0042t0003g0106others(114): Show | 128 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.824-1428C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585052 | ||||||
chr1:22585053 | GCA | G | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.824-1425_824-1424d others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22585053 | |||||
chr1:22585055 | A | G | 126 | a0000c0007t0035g0006a0000c0041t0001g0031a0000c0042t0003g0106others(123): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.824-1425A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585055 | ||||||
chr1:22585056 | C | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.824-1424C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585056 | ||||||
chr1:22585058 | C | T | 2 | a0001c0002t0005g0022a0001c0002t0005g0064 | 3 | HG01070.hp2 HG01071.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.824-1422C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585058 | ||||||
chr1:22585159 | C | A | 1 | a0001c0006t0005g0284 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.824-1321C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585159 | ||||||
chr1:22585159 | C | G | 131 | a0000c0007t0035g0006a0000c0041t0001g0031a0000c0042t0003g0106others(128): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.824-1321C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585159 | ||||||
chr1:22585173 | C | T | 1 | a0002c0040t0009g0030 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.824-1307C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585173 | ||||||
chr1:22585206 | C | T | 3 | a0003c0014t0015g0023a0003c0014t0015g0302a0004c0044t0002g0296 | 4 | HG00642.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1274C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585206 | ||||||
chr1:22585341 | A | G | 131 | a0000c0007t0035g0006a0000c0041t0001g0031a0000c0042t0003g0106others(128): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.824-1139A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585341 | ||||||
chr1:22585512 | T | A | 6 | a0001c0002t0039g0300a0001c0013t0017g0306a0001c0013t0017g0307others(3): Show | 6 | HG02040.hp1 HG02615.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-968T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585512 | ||||||
chr1:22585519 | C | T | 1 | a0001c0002t0004g0110 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.824-961C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585519 | ||||||
chr1:22585629 | T | C | 27 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(24): Show | 28 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.824-851T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585629 | ||||||
chr1:22585741 | G | T | 3 | a0001c0002t0004g0221a0001c0002t0005g0022a0001c0002t0005g0064 | 4 | HG01070.hp2 HG01071.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-739G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585741 | ||||||
chr1:22585802 | C | T | 4 | a0001c0001t0003g0184a0001c0001t0003g0194a0001c0001t0003g0196others(1): Show | 4 | HG01346.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-678C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585802 | ||||||
chr1:22585819 | C | G | 17 | a0001c0002t0004g0221a0001c0002t0005g0022a0001c0002t0005g0064others(14): Show | 21 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.824-661C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585819 | ||||||
chr1:22585847 | C | G | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.824-633C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585847 | ||||||
chr1:22585882 | T | A | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.824-598T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585882 | ||||||
chr1:22585912 | A | G | 70 | a0000c0007t0010g0158a0000c0041t0001g0031a0000c0042t0003g0106others(67): Show | 72 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.824-568A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585912 | ||||||
chr1:22585947 | C | T | 84 | a0000c0007t0010g0158a0000c0041t0001g0031a0000c0042t0003g0106others(81): Show | 90 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.824-533C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585947 | ||||||
chr1:22585948 | A | G | 168 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(165): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.824-532A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22585948 | ||||||
chr1:22586085 | G | A | 7 | a0001c0006t0004g0288a0001c0006t0005g0282a0001c0006t0005g0283others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-395G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22586085 | ||||||
chr1:22586300 | GC | G | 30 | a0001c0001t0007g0138a0001c0010t0002g0093a0001c0010t0007g0080others(27): Show | 34 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.824-175delC | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 22586300 | |||||
chr1:22586326 | T | C | 310 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0001g0269others(307): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.824-154T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22586326 | ||||||
chr1:22586371 | C | T | 1 | a0001c0005t0003g0035 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.824-109C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22586371 | ||||||
chr1:22586372 | A | G | 168 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(165): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.824-108A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22586372 | ||||||
chr1:22586417 | C | T | 42 | a0000c0007t0010g0158a0001c0001t0002g0011a0001c0001t0002g0133others(39): Show | 43 | HG00438.hp2 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.824-63C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22586417 | ||||||
chr1:22586421 | C | T | 6 | a0001c0001t0001g0210a0001c0002t0006g0014a0001c0002t0006g0211others(3): Show | 7 | HG01123.hp2 HG01256.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-59C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 3/16 | chr1 | 22586421 | ||||||
chr1:22586660 | T | C | 174 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(171): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.979+25T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22586660 | ||||||
chr1:22586780 | T | TGG | 56 | a0000c0007t0010g0158a0001c0001t0002g0011a0001c0001t0002g0133others(53): Show | 58 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.979+152_979+153dup others(2): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 22586780 | |||||
chr1:22586780 | T | TGGG | 18 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0007g0136others(15): Show | 20 | HG00438.hp2 HG00597.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.979+151_979+153dup others(3): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 22586780 | |||||
chr1:22586781 | G | GGGGT | 81 | a0000c0007t0035g0006a0001c0001t0002g0070a0001c0001t0002g0098others(78): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.979+149_979+150ins others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 22586781 | |||||
chr1:22586805 | A | G | 1 | a0001c0001t0019g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.979+170A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22586805 | ||||||
chr1:22586857 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.979+222C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22586857 | ||||||
chr1:22586858 | T | G | 1 | a0001c0001t0003g0194 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.979+223T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22586858 | ||||||
chr1:22586937 | C | T | 1 | a0003c0047t0013g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.979+302C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22586937 | ||||||
chr1:22587037 | C | T | 1 | a0001c0001t0003g0260 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.979+402C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587037 | ||||||
chr1:22587040 | G | T | 1 | a0002c0003t0002g0090 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.979+405G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587040 | ||||||
chr1:22587113 | G | A | 69 | a0001c0001t0002g0070a0001c0001t0002g0098a0001c0001t0002g0143others(66): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.979+478G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587113 | ||||||
chr1:22587169 | G | A | 1 | a0001c0001t0016g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.979+534G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587169 | ||||||
chr1:22587203 | C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0201a0001c0001t0001g0246others(3): Show | 7 | HG00438.hp1 HG01952.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+568C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587203 | ||||||
chr1:22587213 | G | A | 1 | a0001c0002t0003g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.979+578G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587213 | ||||||
chr1:22587306 | T | G | 1 | a0001c0001t0003g0273 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.979+671T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587306 | ||||||
chr1:22587402 | C | T | 3 | a0001c0002t0004g0221a0001c0002t0005g0022a0001c0002t0005g0064 | 4 | HG01070.hp2 HG01071.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+767C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587402 | ||||||
chr1:22587427 | G | T | 69 | a0001c0001t0002g0070a0001c0001t0002g0098a0001c0001t0002g0143others(66): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.979+792G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587427 | ||||||
chr1:22587469 | C | T | 1 | a0001c0005t0003g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.979+834C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587469 | ||||||
chr1:22587490 | G | A | 70 | a0001c0001t0001g0303a0001c0001t0002g0070a0001c0001t0002g0098others(67): Show | 75 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.979+855G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587490 | ||||||
chr1:22587500 | A | G | 172 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(169): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.979+865A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587500 | ||||||
chr1:22587614 | G | T | 70 | a0000c0007t0010g0158a0000c0041t0001g0031a0000c0042t0003g0106others(67): Show | 72 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.979+979G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587614 | ||||||
chr1:22587667 | G | C | 22 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(19): Show | 23 | HG00733.hp2 HG00735.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.979+1032G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587667 | ||||||
chr1:22587888 | C | T | 1 | a0002c0003t0002g0002 | 3 | HG00642.hp2 HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.980-983C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22587888 | ||||||
chr1:22588223 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.980-648C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588223 | ||||||
chr1:22588251 | A | ACCCCAGC others(9): Show |
3 | a0001c0001t0024g0162a0001c0002t0004g0221a0001c0020t0012g0024 | 3 | HG01891.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.980-606_980-605ins others(16): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 22588251 | |||||
chr1:22588266 | A | G | 185 | a0000c0007t0003g0197a0000c0007t0010g0158a0000c0007t0035g0006others(182): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.980-605A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588266 | ||||||
chr1:22588280 | G | A | 71 | a0000c0007t0010g0158a0000c0041t0001g0031a0000c0042t0003g0106others(68): Show | 74 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.980-591G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588280 | ||||||
chr1:22588358 | G | A | 168 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(165): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.980-513G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588358 | ||||||
chr1:22588370 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-501C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588370 | ||||||
chr1:22588470 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.980-401G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588470 | ||||||
chr1:22588537 | T | C | 175 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(172): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.980-334T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588537 | ||||||
chr1:22588588 | G | A | 165 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(162): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.980-283G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588588 | ||||||
chr1:22588618 | C | T | 18 | a0001c0001t0002g0098a0001c0011t0010g0142a0001c0022t0004g0027others(15): Show | 21 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.980-253C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588618 | ||||||
chr1:22588680 | G | A | 21 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(18): Show | 22 | HG00733.hp2 HG01192.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.980-191G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588680 | ||||||
chr1:22588689 | G | A | 23 | a0001c0001t0002g0098a0001c0011t0010g0142a0001c0013t0017g0306others(20): Show | 26 | HG01109.hp1 HG02040.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.980-182G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 4/16 | chr1 | 22588689 | ||||||
chr1:22589260 | T | C | 173 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(170): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1315+54T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589260 | ||||||
chr1:22589295 | C | T | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1315+89C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589295 | ||||||
chr1:22589365 | C | T | 27 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(24): Show | 28 | HG00733.hp2 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1315+159C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589365 | ||||||
chr1:22589398 | A | T | 31 | a0001c0001t0007g0138a0001c0010t0002g0093a0001c0010t0007g0080others(28): Show | 35 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1315+192A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589398 | ||||||
chr1:22589446 | C | T | 1 | a0001c0002t0004g0141 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1315+240C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589446 | ||||||
chr1:22589473 | T | G | 1 | a0001c0002t0044g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1315+267T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589473 | ||||||
chr1:22589474 | C | G | 10 | a0001c0002t0040g0060a0001c0006t0004g0288a0001c0006t0005g0207others(7): Show | 10 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.1315+268C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589474 | ||||||
chr1:22589485 | A | T | 174 | a0000c0007t0010g0158a0000c0007t0035g0006a0000c0041t0001g0031others(171): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1315+279A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589485 | ||||||
chr1:22589506 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1315+300G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589506 | ||||||
chr1:22589699 | AG | A | 10 | a0001c0002t0040g0060a0001c0006t0004g0288a0001c0006t0005g0207others(7): Show | 10 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.1315+494delG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589699 | ||||||
chr1:22589799 | C | T | 1 | a0001c0002t0004g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1315+593C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589799 | ||||||
chr1:22589800 | G | A | 3 | a0001c0001t0002g0098a0001c0022t0004g0027a0001c0022t0004g0028 | 3 | HG02559.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1315+594G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589800 | ||||||
chr1:22589928 | C | T | 1 | a0001c0002t0004g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1315+722C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22589928 | ||||||
chr1:22590050 | A | G | 12 | a0000c0007t0035g0006a0001c0001t0003g0021a0001c0001t0003g0051others(9): Show | 14 | HG01099.hp2 HG01884.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1315+844A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590050 | ||||||
chr1:22590127 | G | A | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1315+921G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590127 | ||||||
chr1:22590175 | A | G | 1 | a0002c0003t0002g0096 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1315+969A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590175 | ||||||
chr1:22590178 | G | A | 41 | a0001c0001t0007g0138a0001c0002t0040g0060a0001c0006t0005g0207others(38): Show | 45 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1315+972G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590178 | ||||||
chr1:22590247 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+1041C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590247 | ||||||
chr1:22590364 | C | T | 1 | a0001c0001t0003g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1315+1158C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590364 | ||||||
chr1:22590371 | T | C | 106 | a0000c0007t0035g0006a0001c0001t0002g0011a0001c0001t0002g0070others(103): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1315+1165T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590371 | ||||||
chr1:22590419 | C | T | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+1213C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590419 | ||||||
chr1:22590526 | T | A | 3 | a0001c0011t0008g0134a0001c0011t0010g0142a0001c0011t0038g0069 | 3 | HG02622.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1315+1320T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590526 | ||||||
chr1:22590564 | G | C | 5 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308others(2): Show | 5 | HG02040.hp1 NA18957.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+1358G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590564 | ||||||
chr1:22590628 | C | T | 3 | a0005c0019t0004g0147a0005c0019t0004g0148a0018c0035t0008g0155 | 3 | HG01109.hp1 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1315+1422C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590628 | ||||||
chr1:22590747 | TTTG | T | 46 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0001t0001g0019others(43): Show | 48 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1315+1542_1315+154 others(7): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590747 | ||||||
chr1:22590785 | G | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0202a0001c0001t0001g0247others(3): Show | 6 | HG00323.hp2 HG02004.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1315+1579G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590785 | ||||||
chr1:22590808 | C | T | 1 | a0001c0005t0003g0033 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1315+1602C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590808 | ||||||
chr1:22590824 | C | A | 1 | a0001c0001t0002g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1315+1618C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590824 | ||||||
chr1:22590956 | C | A | 1 | a0001c0002t0007g0173 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1315+1750C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22590956 | ||||||
chr1:22591020 | C | T | 1 | a0001c0002t0004g0112 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1315+1814C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591020 | ||||||
chr1:22591066 | T | C | 43 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(40): Show | 44 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1315+1860T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591066 | ||||||
chr1:22591161 | G | A | 251 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0001g0269others(248): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1315+1955G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591161 | ||||||
chr1:22591235 | T | A | 58 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1315+2029T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591235 | ||||||
chr1:22591293 | C | T | 1 | a0001c0002t0026g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1316-2033C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591293 | ||||||
chr1:22591294 | G | A | 1 | a0001c0002t0039g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1316-2032G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591294 | ||||||
chr1:22591316 | C | T | 2 | a0001c0013t0017g0307a0001c0013t0017g0308 | 2 | NA18957.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1316-2010C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591316 | ||||||
chr1:22591317 | G | A | 16 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0003g0021others(13): Show | 18 | HG01069.hp1 HG01099.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1316-2009G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591317 | ||||||
chr1:22591332 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1316-1994C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591332 | ||||||
chr1:22591333 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1316-1993T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591333 | ||||||
chr1:22591350 | A | G | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1316-1976A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591350 | ||||||
chr1:22591388 | A | AT | 57 | a0001c0001t0001g0252a0001c0001t0007g0135a0001c0001t0007g0136others(54): Show | 58 | HG00438.hp2 HG00597.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1316-1925dupT | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 22591388 | |||||
chr1:22591388 | A | ATT | 42 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0003g0021others(39): Show | 48 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1316-1926_1316-192 others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 22591388 | |||||
chr1:22591444 | C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG02074.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1316-1882C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591444 | ||||||
chr1:22591574 | A | G | 1 | a0001c0002t0004g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1316-1752A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591574 | ||||||
chr1:22591616 | A | T | 11 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(8): Show | 11 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1316-1710A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591616 | ||||||
chr1:22591797 | C | T | 9 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(6): Show | 11 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1316-1529C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591797 | ||||||
chr1:22591874 | G | A | 7 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(4): Show | 9 | HG02055.hp2 HG02818.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1316-1452G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591874 | ||||||
chr1:22591954 | T | C | 1 | a0008c0034t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1316-1372T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591954 | ||||||
chr1:22591984 | A | T | 2 | a0000c0007t0010g0158a0001c0001t0008g0145 | 2 | HG00735.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1316-1342A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22591984 | ||||||
chr1:22592017 | C | T | 1 | a0001c0002t0006g0215 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1316-1309C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592017 | ||||||
chr1:22592085 | G | A | 1 | a0001c0028t0003g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1316-1241G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592085 | ||||||
chr1:22592317 | G | A | 1 | a0002c0043t0002g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1316-1009G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592317 | ||||||
chr1:22592353 | G | A | 1 | a0001c0046t0037g0297 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1316-973G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592353 | ||||||
chr1:22592448 | C | A | 11 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(8): Show | 11 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1316-878C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592448 | ||||||
chr1:22592582 | C | T | 1 | a0001c0010t0007g0080 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1316-744C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592582 | ||||||
chr1:22592595 | G | A | 15 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(12): Show | 16 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1316-731G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592595 | ||||||
chr1:22592673 | G | A | 11 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(8): Show | 11 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1316-653G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592673 | ||||||
chr1:22592739 | C | T | 1 | a0001c0002t0006g0295 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1316-587C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592739 | ||||||
chr1:22592787 | C | T | 1 | a0002c0004t0034g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1316-539C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592787 | ||||||
chr1:22592799 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1316-527G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592799 | ||||||
chr1:22592800 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1316-526A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592800 | ||||||
chr1:22592801 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1316-525G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592801 | ||||||
chr1:22592832 | C | T | 1 | a0002c0004t0034g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1316-494C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592832 | ||||||
chr1:22592836 | G | A | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1316-490G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592836 | ||||||
chr1:22592896 | C | T | 1 | a0001c0013t0017g0306 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1316-430C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592896 | ||||||
chr1:22592981 | T | C | 1 | a0018c0035t0008g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1316-345T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22592981 | ||||||
chr1:22593042 | C | T | 2 | a0001c0001t0003g0276a0011c0025t0003g0278 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1316-284C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22593042 | ||||||
chr1:22593211 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1316-115A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22593211 | ||||||
chr1:22593298 | G | A | 2 | a0000c0007t0001g0005a0001c0001t0001g0005 | 3 | NA18959.hp2 NA18982.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1316-28G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22593298 | ||||||
chr1:22593308 | C | T | 1 | a0002c0003t0002g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1316-18C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22593308 | ||||||
chr1:22593318 | C | T | 1 | a0001c0005t0003g0035 | 1 | NA18945.hp2 | splice_region_variant&intron_variant | LOW | c.1316-8C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 5/16 | chr1 | 22593318 | ||||||
chr1:22593467 | G | A | 1 | a0001c0002t0022g0159 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1440+17G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 6/16 | chr1 | 22593467 | ||||||
chr1:22593512 | G | A | 2 | a0001c0002t0002g0012a0007c0023t0002g0012 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1441-12G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 6/16 | chr1 | 22593512 | ||||||
chr1:22593764 | A | G | 1 | a0001c0006t0005g0282 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1603+78A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22593764 | ||||||
chr1:22593771 | G | A | 1 | a0005c0019t0004g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603+85G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22593771 | ||||||
chr1:22594022 | G | A | 16 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(13): Show | 17 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1603+336G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594022 | ||||||
chr1:22594133 | A | T | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1603+447A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594133 | ||||||
chr1:22594169 | A | G | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1603+483A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594169 | ||||||
chr1:22594261 | C | T | 7 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(4): Show | 9 | HG02055.hp2 HG02818.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603+575C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594261 | ||||||
chr1:22594330 | C | T | 11 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(8): Show | 11 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1603+644C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594330 | ||||||
chr1:22594407 | G | A | 2 | a0001c0002t0004g0123a0001c0002t0004g0131 | 2 | HG01081.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1603+721G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594407 | ||||||
chr1:22594435 | C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | NA18966.hp1 NA18967.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+749C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594435 | ||||||
chr1:22594511 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1604-719G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594511 | ||||||
chr1:22594647 | G | A | 1 | a0001c0002t0022g0159 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1604-583G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594647 | ||||||
chr1:22594679 | G | A | 1 | a0001c0002t0003g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1604-551G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594679 | ||||||
chr1:22594751 | A | G | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1604-479A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594751 | ||||||
chr1:22594763 | G | A | 8 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.1604-467G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594763 | ||||||
chr1:22594958 | C | G | 1 | a0001c0020t0012g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1604-272C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594958 | ||||||
chr1:22594970 | A | C | 36 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(33): Show | 39 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1604-260A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22594970 | ||||||
chr1:22595010 | T | C | 162 | a0000c0007t0035g0006a0001c0001t0002g0011a0001c0001t0002g0070others(159): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1604-220T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22595010 | ||||||
chr1:22595032 | T | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(17): Show | 21 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1604-198T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22595032 | ||||||
chr1:22595086 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1604-144C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 7/16 | chr1 | 22595086 | ||||||
chr1:22595430 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1697+107T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595430 | ||||||
chr1:22595533 | T | G | 161 | a0000c0007t0035g0006a0001c0001t0002g0011a0001c0001t0002g0070others(158): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1697+210T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595533 | ||||||
chr1:22595592 | G | A | 1 | a0001c0002t0044g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1697+269G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595592 | ||||||
chr1:22595707 | T | C | 2 | a0001c0027t0003g0244a0001c0028t0003g0243 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1697+384T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595707 | ||||||
chr1:22595808 | C | T | 1 | a0003c0018t0047g0160 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1698-298C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595808 | ||||||
chr1:22595817 | T | G | 2 | a0001c0001t0019g0261a0001c0045t0019g0047 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1698-289T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595817 | ||||||
chr1:22595897 | C | T | 1 | a0001c0021t0012g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1698-209C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595897 | ||||||
chr1:22595919 | G | A | 23 | a0001c0002t0006g0014a0001c0002t0006g0100a0001c0002t0006g0208others(20): Show | 24 | HG00639.hp1 HG01109.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1698-187G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595919 | ||||||
chr1:22595944 | C | G | 56 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0003g0021others(53): Show | 65 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1698-162C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595944 | ||||||
chr1:22595945 | C | T | 13 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(10): Show | 14 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1698-161C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22595945 | ||||||
chr1:22596000 | A | C | 1 | a0001c0001t0008g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1698-106A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22596000 | ||||||
chr1:22596011 | C | T | 1 | a0001c0002t0040g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1698-95C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22596011 | ||||||
chr1:22596053 | G | A | 128 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0003g0021others(125): Show | 138 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.1698-53G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22596053 | ||||||
chr1:22596067 | G | A | 190 | a0000c0007t0035g0006a0000c0041t0001g0031a0000c0042t0003g0106others(187): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1698-39G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 8/16 | chr1 | 22596067 | ||||||
chr1:22596229 | T | C | 56 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0003g0021others(53): Show | 65 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1765+56T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596229 | ||||||
chr1:22596292 | AG | A | 3 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308 | 3 | NA18957.hp2 NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1765+120delG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596292 | ||||||
chr1:22596307 | G | A | 48 | a0001c0001t0009g0257a0001c0002t0002g0149a0001c0002t0002g0150others(45): Show | 49 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.1765+134G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596307 | ||||||
chr1:22596339 | G | A | 2 | a0004c0012t0002g0007a0004c0012t0002g0025 | 3 | HG02145.hp1 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1765+166G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596339 | ||||||
chr1:22596344 | G | A | 3 | a0001c0001t0001g0222a0001c0001t0007g0101a0001c0001t0007g0102 | 3 | HG00099.hp1 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1765+171G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596344 | ||||||
chr1:22596535 | C | A | 7 | a0001c0002t0004g0107a0001c0002t0004g0110a0001c0002t0004g0111others(4): Show | 7 | HG00438.hp2 HG00738.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1765+362C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596535 | ||||||
chr1:22596535 | C | T | 62 | a0000c0007t0035g0006a0001c0001t0002g0098a0001c0001t0003g0021others(59): Show | 70 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1765+362C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596535 | ||||||
chr1:22596536 | A | G | 158 | a0000c0007t0035g0006a0001c0001t0002g0011a0001c0001t0002g0070others(155): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1765+363A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596536 | ||||||
chr1:22596568 | A | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0233 | 2 | NA18948.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1765+395A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596568 | ||||||
chr1:22596654 | T | A | 1 | a0001c0006t0005g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1765+481T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596654 | ||||||
chr1:22596670 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1765+497T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596670 | ||||||
chr1:22596718 | G | A | 1 | a0001c0002t0044g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1765+545G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596718 | ||||||
chr1:22596796 | A | G | 3 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308 | 3 | NA18957.hp2 NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1766-516A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596796 | ||||||
chr1:22596805 | G | A | 1 | a0001c0008t0012g0010 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1766-507G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596805 | ||||||
chr1:22596815 | T | C | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1766-497T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22596815 | ||||||
chr1:22597043 | A | G | 5 | a0003c0014t0015g0023a0003c0014t0015g0302a0004c0012t0002g0007others(2): Show | 7 | HG00642.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1766-269A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22597043 | ||||||
chr1:22597070 | G | GA | 4 | a0001c0001t0001g0222a0001c0001t0007g0101a0001c0001t0007g0102others(1): Show | 4 | HG00099.hp1 HG01123.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1766-238dupA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr1 | 22597070 | |||||
chr1:22597176 | C | T | 1 | a0001c0002t0005g0022 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1766-136C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22597176 | ||||||
chr1:22597196 | C | A | 8 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.1766-116C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22597196 | ||||||
chr1:22597239 | CCCAGGCC others(4): Show |
C | 8 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.1766-72_1766-62del others(11): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22597239 | ||||||
chr1:22597292 | G | A | 8 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.1766-20G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 9/16 | chr1 | 22597292 | ||||||
chr1:22597530 | C | T | 2 | a0001c0002t0005g0073a0001c0002t0005g0074 | 2 | NA18948.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1930+54C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 10/16 | chr1 | 22597530 | ||||||
chr1:22597631 | G | A | 8 | a0001c0006t0004g0288a0001c0006t0005g0207a0001c0006t0005g0212others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.1931-45G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 10/16 | chr1 | 22597631 | ||||||
chr1:22597871 | G | A | 12 | a0001c0002t0002g0012a0001c0006t0004g0288a0001c0006t0005g0207others(9): Show | 12 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.2116+10G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 11/16 | chr1 | 22597871 | ||||||
chr1:22597910 | G | T | 2 | a0001c0001t0024g0162a0006c0038t0024g0161 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2116+49G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 11/16 | chr1 | 22597910 | ||||||
chr1:22597925 | T | C | 59 | a0001c0001t0009g0257a0001c0001t0010g0168a0001c0002t0002g0149others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.2116+64T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 11/16 | chr1 | 22597925 | ||||||
chr1:22597940 | A | G | 1 | a0001c0046t0037g0297 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2116+79A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 11/16 | chr1 | 22597940 | ||||||
chr1:22597971 | T | C | 70 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(67): Show | 77 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2116+110T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 11/16 | chr1 | 22597971 | ||||||
chr1:22598043 | GT | G | 55 | a0001c0001t0009g0257a0001c0002t0002g0012a0001c0002t0002g0149others(52): Show | 58 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.2117-105delT | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 22598043 | |||||
chr1:22598250 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2178+38G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598250 | ||||||
chr1:22598254 | G | A | 1 | a0002c0003t0002g0082 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2178+42G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598254 | ||||||
chr1:22598255 | A | G | 1 | a0002c0003t0002g0082 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2178+43A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598255 | ||||||
chr1:22598290 | C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0202a0001c0001t0001g0247others(3): Show | 6 | HG00323.hp2 HG02004.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2178+78C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598290 | ||||||
chr1:22598314 | G | A | 12 | a0001c0002t0002g0012a0001c0002t0003g0280a0001c0002t0010g0165others(9): Show | 12 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2178+102G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598314 | ||||||
chr1:22598362 | G | A | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2178+150G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598362 | ||||||
chr1:22598802 | G | A | 2 | a0001c0002t0002g0012a0007c0023t0002g0012 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2179-36G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598802 | ||||||
chr1:22598824 | A | G | 1 | a0004c0044t0002g0296 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2179-14A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 12/16 | chr1 | 22598824 | ||||||
chr1:22599057 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2388+10C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599057 | ||||||
chr1:22599062 | C | G | 1 | a0001c0002t0003g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2388+15C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599062 | ||||||
chr1:22599120 | C | A | 95 | a0001c0001t0009g0257a0001c0002t0002g0012a0001c0002t0002g0149others(92): Show | 102 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2388+73C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599120 | ||||||
chr1:22599155 | G | A | 15 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(12): Show | 16 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.2388+108G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599155 | ||||||
chr1:22599271 | C | A | 14 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(11): Show | 15 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2388+224C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599271 | ||||||
chr1:22599528 | G | A | 96 | a0001c0001t0002g0098a0001c0001t0009g0257a0001c0001t0024g0162others(93): Show | 101 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.2388+481G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599528 | ||||||
chr1:22599603 | G | GAGGGAGG others(21): Show |
2 | a0001c0002t0006g0208a0001c0002t0006g0215 | 2 | HG00639.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2388+574_2388+575i others(30): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599603 | |||||
chr1:22599605 | GGGAGGGA others(46): Show |
G | 17 | a0001c0002t0003g0280a0001c0002t0010g0165a0001c0006t0004g0288others(14): Show | 18 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.2388+575_2388+627d others(55): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599605 | |||||
chr1:22599620 | AGAAGGGA others(14): Show |
A | 7 | a0001c0006t0005g0207a0001c0006t0005g0212a0001c0006t0005g0282others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2388+575_2388+595d others(23): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599620 | |||||
chr1:22599621 | G | A | 1 | a0002c0003t0002g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2388+574G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599621 | ||||||
chr1:22599622 | A | G | 114 | a0001c0001t0002g0098a0001c0001t0009g0257a0001c0001t0024g0162others(111): Show | 123 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.2388+575A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599622 | ||||||
chr1:22599631 | AAGGAAGG others(98): Show |
A | 1 | a0001c0002t0045g0172 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2388+588_2388+692d others(2): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599631 | |||||
chr1:22599635 | A | G | 18 | a0001c0002t0006g0014a0001c0002t0006g0100a0001c0002t0006g0209others(15): Show | 20 | HG00733.hp2 HG01192.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2388+588A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599635 | ||||||
chr1:22599635 | AAGGGAGG others(94): Show |
A | 2 | a0001c0002t0004g0221a0001c0002t0005g0064 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2388+600_2388+700d others(2): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599635 | |||||
chr1:22599637 | G | A | 2 | a0001c0002t0006g0208a0001c0002t0006g0215 | 2 | HG00639.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2388+590G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599637 | ||||||
chr1:22599637 | GGGAGGGA others(90): Show |
G | 44 | a0001c0001t0009g0257a0001c0002t0002g0149a0001c0002t0002g0150others(41): Show | 45 | HG00438.hp2 HG00738.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.2388+602_2388+698d others(99): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599637 | |||||
chr1:22599641 | G | GGGAGGGA others(25): Show |
1 | a0001c0001t0001g0259 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2388+641_2388+672d others(34): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599641 | |||||
chr1:22599641 | GGGAGGGA others(25): Show |
G | 33 | a0001c0002t0002g0012a0001c0002t0039g0300a0001c0002t0040g0060others(30): Show | 37 | HG00642.hp2 HG00733.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.2388+641_2388+672d others(34): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599641 | |||||
chr1:22599644 | AGGGAAGG others(67): Show |
A | 18 | a0001c0002t0006g0014a0001c0002t0006g0100a0001c0002t0006g0209others(15): Show | 20 | HG00733.hp2 HG01192.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2388+600_2388+673d others(76): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599644 | |||||
chr1:22599648 | AAGGAAGG others(63): Show |
A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2388+602_2388+671d others(72): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599648 | ||||||
chr1:22599653 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+606A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599653 | ||||||
chr1:22599653 | AGGAAAGG others(62): Show |
A | 2 | a0001c0001t0024g0162a0006c0038t0024g0161 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2388+610_2388+678d others(71): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599653 | |||||
chr1:22599656 | A | AGGG | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+609_2388+610i others(5): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599656 | ||||||
chr1:22599658 | A | G | 7 | a0001c0006t0005g0207a0001c0006t0005g0212a0001c0006t0005g0282others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2388+611A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599658 | ||||||
chr1:22599660 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+613G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599660 | ||||||
chr1:22599660 | G | GA | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+614dupA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599660 | |||||
chr1:22599667 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+620G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599667 | ||||||
chr1:22599672 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+625A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599672 | ||||||
chr1:22599681 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+634A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599681 | ||||||
chr1:22599684 | AAGGAAAG others(1): Show |
A | 7 | a0001c0006t0005g0207a0001c0006t0005g0212a0001c0006t0005g0282others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2388+641_2388+648d others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599684 | |||||
chr1:22599684 | AAGGAAAG others(45): Show |
A | 1 | a0002c0003t0002g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2388+641_2388+692d others(54): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599684 | |||||
chr1:22599686 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+639G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599686 | ||||||
chr1:22599688 | A | G | 16 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(13): Show | 18 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2388+641A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599688 | ||||||
chr1:22599690 | A | G | 33 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(30): Show | 36 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.2388+643A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599690 | ||||||
chr1:22599696 | G | GA | 13 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(10): Show | 14 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2388+650dupA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599696 | |||||
chr1:22599696 | G | GAGGAAGG others(92): Show |
3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+652_2388+653i others(101): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599696 | |||||
chr1:22599698 | G | A | 2 | a0001c0001t0001g0249a0001c0001t0002g0098 | 2 | HG00609.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2388+651G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599698 | ||||||
chr1:22599700 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+653G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599700 | ||||||
chr1:22599702 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+655G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599702 | ||||||
chr1:22599706 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+659G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599706 | ||||||
chr1:22599709 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+662G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599709 | ||||||
chr1:22599711 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+664G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599711 | ||||||
chr1:22599715 | GA | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+670delA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599715 | |||||
chr1:22599716 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2388+669A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599716 | ||||||
chr1:22599716 | AAGGGAGG others(13): Show |
A | 47 | a0001c0002t0002g0012a0001c0002t0039g0300a0001c0002t0040g0060others(44): Show | 52 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2388+681_2388+700d others(22): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599716 | |||||
chr1:22599722 | G | A | 26 | a0001c0002t0006g0014a0001c0002t0006g0100a0001c0002t0006g0209others(23): Show | 30 | HG00733.hp2 HG01192.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.2388+675G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599722 | ||||||
chr1:22599724 | G | GA | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+678dupA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599724 | |||||
chr1:22599726 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2388+679G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599726 | ||||||
chr1:22599730 | A | G | 4 | a0001c0001t0009g0062a0001c0006t0004g0288a0003c0014t0015g0023others(1): Show | 5 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2388+683A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599730 | ||||||
chr1:22599731 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+684G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599731 | ||||||
chr1:22599733 | A | G | 13 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(10): Show | 14 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2388+686A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599733 | ||||||
chr1:22599733 | AAGG | A | 30 | a0001c0001t0001g0199a0001c0001t0024g0162a0001c0002t0006g0014others(27): Show | 34 | HG00733.hp2 HG01192.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.2388+690_2388+692d others(5): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599733 | |||||
chr1:22599736 | G | GA | 170 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0001g0269others(167): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2388+690dupA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599736 | |||||
chr1:22599736 | G | GAAGGAGG others(14): Show |
13 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(10): Show | 14 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2388+690_2388+691i others(23): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599736 | |||||
chr1:22599747 | G | T | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+700G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599747 | ||||||
chr1:22599749 | A | G | 4 | a0001c0001t0002g0098a0001c0001t0009g0062a0003c0014t0015g0023others(1): Show | 5 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2388+702A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599749 | ||||||
chr1:22599752 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+705A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599752 | ||||||
chr1:22599753 | G | A | 12 | a0001c0001t0002g0098a0001c0001t0009g0062a0002c0004t0011g0061others(9): Show | 15 | HG00642.hp1 HG02055.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2388+706G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599753 | ||||||
chr1:22599756 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+709A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599756 | ||||||
chr1:22599758 | A | G | 4 | a0001c0001t0002g0098a0001c0001t0009g0062a0003c0014t0015g0023others(1): Show | 5 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2388+711A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599758 | ||||||
chr1:22599760 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+713A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599760 | ||||||
chr1:22599766 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+719G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599766 | ||||||
chr1:22599767 | A | AGG | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+721_2388+722i others(4): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599767 | |||||
chr1:22599767 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+720A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599767 | ||||||
chr1:22599772 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+725G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599772 | ||||||
chr1:22599776 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+729A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599776 | ||||||
chr1:22599779 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+732G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599779 | ||||||
chr1:22599783 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+736A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599783 | ||||||
chr1:22599784 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+737G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599784 | ||||||
chr1:22599787 | A | AG | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+740_2388+741i others(3): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599787 | ||||||
chr1:22599788 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+741A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599788 | ||||||
chr1:22599792 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+745A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599792 | ||||||
chr1:22599798 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+751G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599798 | ||||||
chr1:22599802 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+755A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599802 | ||||||
chr1:22599806 | A | AGGCGGGA others(131): Show |
2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2388+761_2388+762i others(140): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599806 | |||||
chr1:22599806 | A | AGGCGGGA others(120): Show |
1 | a0001c0001t0009g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2388+761_2388+762i others(129): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599806 | |||||
chr1:22599809 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+762A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599809 | ||||||
chr1:22599811 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+764A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599811 | ||||||
chr1:22599813 | A | G | 4 | a0001c0001t0002g0098a0001c0001t0009g0062a0003c0014t0015g0023others(1): Show | 5 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2388+766A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599813 | ||||||
chr1:22599816 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+769A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599816 | ||||||
chr1:22599818 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+771A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599818 | ||||||
chr1:22599820 | A | G | 1 | a0001c0008t0006g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2388+773A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599820 | ||||||
chr1:22599827 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+780G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599827 | ||||||
chr1:22599827 | G | GA | 289 | a0000c0007t0001g0218a0000c0007t0001g0269a0000c0007t0010g0158others(286): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2388+781dupA | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599827 | |||||
chr1:22599827 | G | GAAGGGGA others(96): Show |
3 | a0000c0007t0001g0005a0001c0001t0001g0005a0001c0001t0001g0198 | 4 | NA18957.hp1 NA18959.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+781_2388+782i others(105): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599827 | |||||
chr1:22599827 | G | GAAGGGGA others(465): Show |
11 | a0000c0007t0003g0197a0001c0001t0001g0202a0001c0001t0003g0186others(8): Show | 11 | HG00323.hp2 HG00621.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2388+781_2388+782i others(474): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599827 | |||||
chr1:22599827 | G | GAAGGGGA others(903): Show |
1 | a0001c0001t0010g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2388+781_2388+782i others(912): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599827 | |||||
chr1:22599827 | G | GAAGGGGA others(462): Show |
4 | a0001c0001t0003g0184a0001c0001t0003g0194a0001c0001t0003g0196others(1): Show | 4 | HG01346.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+781_2388+782i others(471): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599827 | |||||
chr1:22599830 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+783G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599830 | ||||||
chr1:22599831 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+784G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599831 | ||||||
chr1:22599833 | AG | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+789delG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599833 | |||||
chr1:22599838 | A | G | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+791A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599838 | ||||||
chr1:22599844 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+797G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599844 | ||||||
chr1:22599850 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2388+803G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599850 | ||||||
chr1:22599850 | G | GGAT | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2388+804_2388+805i others(5): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599850 | |||||
chr1:22599861 | G | A | 3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389-800G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599861 | ||||||
chr1:22599861 | GAGGA | G | 3 | a0001c0001t0002g0098a0001c0005t0020g0042a0001c0005t0020g0043 | 3 | HG03453.hp1 NA18980.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2389-796_2389-793d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599861 | |||||
chr1:22599865 | A | AAGGGAAG others(9): Show |
15 | a0000c0007t0035g0006a0001c0001t0003g0021a0001c0001t0003g0051others(12): Show | 17 | HG01069.hp1 HG01099.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2389-787_2389-786i others(18): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599865 | |||||
chr1:22599865 | A | AGGGAAGG others(1): Show |
3 | a0001c0001t0009g0062a0003c0014t0015g0023a0003c0014t0015g0302 | 4 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2389-796_2389-795i others(10): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599865 | ||||||
chr1:22599868 | G | A | 6 | a0001c0001t0002g0098a0001c0001t0009g0062a0001c0005t0020g0042others(3): Show | 7 | HG00642.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2389-793G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599868 | ||||||
chr1:22599868 | G | GGAAGGAA others(306): Show |
1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-787_2389-786i others(315): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599868 | |||||
chr1:22599868 | G | GGAAGGAA others(30): Show |
23 | a0000c0042t0003g0106a0001c0001t0003g0189a0001c0002t0008g0118others(20): Show | 23 | HG00735.hp2 HG01106.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2389-787_2389-786i others(39): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599868 | |||||
chr1:22599868 | G | GGAAGGAA others(307): Show |
12 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(9): Show | 13 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2389-787_2389-786i others(316): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599868 | |||||
chr1:22599873 | G | GAAGGAAG others(40): Show |
1 | a0000c0041t0001g0031 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2389-787_2389-786i others(49): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599873 | |||||
chr1:22599894 | A | G | 1 | a0001c0033t0006g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2389-767A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599894 | ||||||
chr1:22599914 | A | G | 1 | a0001c0002t0002g0151 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2389-747A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599914 | ||||||
chr1:22599922 | G | A | 313 | a0000c0007t0001g0005a0000c0007t0001g0218a0000c0007t0001g0269others(310): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2389-739G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599922 | ||||||
chr1:22599938 | GGGGA | G | 19 | a0001c0001t0001g0250a0001c0001t0002g0011a0001c0001t0002g0070others(16): Show | 21 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2389-704_2389-701d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22599938 | |||||
chr1:22599970 | C | A | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-691C>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599970 | ||||||
chr1:22599981 | G | A | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-680G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599981 | ||||||
chr1:22599984 | A | C | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-677A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599984 | ||||||
chr1:22599987 | A | G | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-674A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599987 | ||||||
chr1:22599993 | A | G | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-668A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599993 | ||||||
chr1:22599999 | G | A | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-662G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22599999 | ||||||
chr1:22600024 | G | A | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-637G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600024 | ||||||
chr1:22600031 | A | G | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-630A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600031 | ||||||
chr1:22600034 | G | A | 14 | a0000c0007t0035g0006a0001c0001t0003g0021a0001c0001t0003g0051others(11): Show | 16 | HG01069.hp1 HG01099.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2389-627G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600034 | ||||||
chr1:22600048 | A | T | 1 | a0010c0024t0046g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2389-613A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600048 | ||||||
chr1:22600067 | T | C | 84 | a0001c0001t0002g0098a0001c0001t0024g0162a0001c0001t0025g0026others(81): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.2389-594T>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600067 | ||||||
chr1:22600067 | TGGAG | T | 12 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(9): Show | 12 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2389-588_2389-585d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600067 | |||||
chr1:22600073 | G | A | 14 | a0000c0007t0035g0006a0001c0001t0003g0021a0001c0001t0003g0051others(11): Show | 16 | HG01069.hp1 HG01099.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2389-588G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600073 | ||||||
chr1:22600088 | G | A | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-573G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600088 | ||||||
chr1:22600091 | G | A | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-570G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600091 | ||||||
chr1:22600098 | A | G | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-563A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600098 | ||||||
chr1:22600103 | A | T | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-558A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600103 | ||||||
chr1:22600105 | A | G | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-556A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600105 | ||||||
chr1:22600120 | A | G | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-541A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600120 | ||||||
chr1:22600125 | A | C | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-536A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600125 | ||||||
chr1:22600132 | A | G | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-529A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600132 | ||||||
chr1:22600137 | A | G | 1 | a0001c0010t0042g0094 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2389-524A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600137 | ||||||
chr1:22600139 | G | A | 1 | a0001c0010t0042g0094 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2389-522G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600139 | ||||||
chr1:22600140 | A | AGGAG | 21 | a0001c0002t0004g0120a0001c0002t0006g0014a0001c0002t0006g0100others(18): Show | 23 | HG00639.hp1 HG01192.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.2389-509_2389-506d others(6): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600140 | |||||
chr1:22600156 | A | G | 9 | a0001c0001t0002g0098a0001c0006t0005g0207a0001c0006t0005g0212others(6): Show | 9 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2389-505A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600156 | ||||||
chr1:22600157 | GGAGGGAG others(16): Show |
G | 1 | a0001c0013t0017g0306 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2389-501_2389-479d others(25): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600157 | |||||
chr1:22600159 | AGGGAGGC others(48): Show |
A | 8 | a0001c0001t0002g0098a0001c0006t0005g0207a0001c0006t0005g0212others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.2389-495_2389-441d others(57): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600159 | |||||
chr1:22600160 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-501G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600160 | ||||||
chr1:22600161 | G | A | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-500G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600161 | ||||||
chr1:22600164 | G | A | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-497G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600164 | ||||||
chr1:22600164 | GGCA | G | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-495_2389-493d others(5): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600164 | |||||
chr1:22600166 | C | G | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-495C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600166 | ||||||
chr1:22600171 | A | C | 1 | a0001c0001t0018g0227 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2389-490A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600171 | ||||||
chr1:22600172 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-489G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600172 | ||||||
chr1:22600177 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-484G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600177 | ||||||
chr1:22600179 | A | G | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-482A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600179 | ||||||
chr1:22600180 | A | G | 9 | a0001c0006t0004g0288a0002c0004t0011g0061a0002c0004t0011g0177others(6): Show | 11 | HG02055.hp2 HG02559.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2389-481A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600180 | ||||||
chr1:22600183 | A | G | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-478A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600183 | ||||||
chr1:22600187 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-474G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600187 | ||||||
chr1:22600188 | G | A | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-473G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600188 | ||||||
chr1:22600190 | A | G | 3 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308 | 3 | NA18957.hp2 NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2389-471A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600190 | ||||||
chr1:22600195 | A | C | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-466A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600195 | ||||||
chr1:22600196 | AG | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-463delG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600196 | |||||
chr1:22600200 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-461G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600200 | ||||||
chr1:22600206 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-455G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600206 | ||||||
chr1:22600211 | A | G | 1 | a0001c0006t0004g0288 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389-450A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600211 | ||||||
chr1:22600213 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-448G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600213 | ||||||
chr1:22600214 | T | A | 9 | a0001c0006t0004g0288a0002c0004t0011g0061a0002c0004t0011g0177others(6): Show | 11 | HG02055.hp2 HG02559.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.2389-447T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600214 | ||||||
chr1:22600215 | G | A | 9 | a0001c0001t0002g0098a0001c0006t0004g0288a0001c0006t0005g0207others(6): Show | 9 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2389-446G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600215 | ||||||
chr1:22600219 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-442G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600219 | ||||||
chr1:22600222 | AAAG | A | 4 | a0000c0007t0035g0006a0001c0001t0008g0006a0001c0001t0008g0301others(1): Show | 5 | HG01069.hp1 HG01099.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2389-433_2389-431d others(5): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600222 | |||||
chr1:22600224 | A | G | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-437A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600224 | ||||||
chr1:22600229 | A | G | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-432A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600229 | ||||||
chr1:22600230 | A | G | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-431A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600230 | ||||||
chr1:22600232 | G | T | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-429G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600232 | ||||||
chr1:22600237 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-424G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600237 | ||||||
chr1:22600240 | G | A | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-421G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600240 | ||||||
chr1:22600242 | A | T | 3 | a0001c0013t0017g0306a0001c0013t0017g0307a0001c0013t0017g0308 | 3 | NA18957.hp2 NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2389-419A>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600242 | ||||||
chr1:22600244 | GGACAGAA | G | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2389-415_2389-409d others(9): Show |
EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 22600244 | |||||
chr1:22600246 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2389-415A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600246 | ||||||
chr1:22600438 | G | A | 1 | a0001c0005t0028g0052 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2389-223G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600438 | ||||||
chr1:22600483 | G | A | 1 | a0002c0004t0011g0177 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2389-178G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600483 | ||||||
chr1:22600574 | C | G | 1 | a0001c0006t0005g0285 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2389-87C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600574 | ||||||
chr1:22600633 | C | T | 17 | a0000c0041t0001g0031a0000c0042t0003g0106a0001c0005t0003g0032others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.2389-28C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 13/16 | chr1 | 22600633 | ||||||
chr1:22600821 | A | G | 191 | a0000c0007t0001g0218a0000c0007t0035g0006a0000c0041t0001g0031others(188): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.2538+11A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 14/16 | chr1 | 22600821 | ||||||
chr1:22600833 | T | G | 168 | a0000c0007t0001g0218a0000c0007t0035g0006a0001c0001t0002g0011others(165): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2538+23T>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 14/16 | chr1 | 22600833 | ||||||
chr1:22600870 | G | A | 1 | a0001c0002t0006g0295 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2539-28G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 14/16 | chr1 | 22600870 | ||||||
chr1:22600891 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01993.hp1 | splice_region_variant&intron_variant | LOW | c.2539-7C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 14/16 | chr1 | 22600891 | ||||||
chr1:22601140 | C | T | 1 | a0002c0037t0002g0078 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2729+52C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601140 | ||||||
chr1:22601141 | C | T | 14 | a0000c0007t0035g0006a0001c0001t0003g0021a0001c0001t0003g0051others(11): Show | 16 | HG01069.hp1 HG01099.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2729+53C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601141 | ||||||
chr1:22601165 | T | A | 3 | a0001c0002t0004g0221a0001c0002t0005g0022a0001c0002t0005g0064 | 4 | HG01070.hp2 HG01071.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.2729+77T>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601165 | ||||||
chr1:22601179 | G | A | 21 | a0001c0002t0006g0014a0001c0002t0006g0100a0001c0002t0006g0208others(18): Show | 23 | HG00639.hp1 HG00733.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.2729+91G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601179 | ||||||
chr1:22601218 | G | T | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2730-82G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601218 | ||||||
chr1:22601221 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2730-79C>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601221 | ||||||
chr1:22601260 | C | T | 2 | a0001c0002t0004g0123a0001c0002t0004g0131 | 2 | HG01081.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2730-40C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601260 | ||||||
chr1:22601274 | A | C | 1 | a0000c0007t0010g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2730-26A>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601274 | ||||||
chr1:22601285 | G | A | 2 | a0003c0014t0015g0023a0003c0014t0015g0302 | 3 | HG00642.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2730-15G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 15/16 | chr1 | 22601285 | ||||||
chr1:22601515 | A | AG | 33 | a0000c0007t0003g0197a0001c0001t0001g0017a0001c0001t0001g0193others(30): Show | 34 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.2903+51dupG | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr1 | 22601515 | |||||
chr1:22601515 | A | G | 1 | a0001c0001t0024g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2903+42A>G | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | chr1 | 22601515 | ||||||
chr1:22601518 | G | C | 1 | a0001c0020t0012g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2903+45G>C | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | chr1 | 22601518 | ||||||
chr1:22601518 | G | T | 1 | a0001c0002t0005g0074 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2903+45G>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | chr1 | 22601518 | ||||||
chr1:22601571 | G | A | 13 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(10): Show | 14 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2904-56G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | chr1 | 22601571 | ||||||
chr1:22601576 | C | T | 13 | a0001c0001t0002g0011a0001c0001t0002g0070a0001c0001t0002g0133others(10): Show | 14 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2904-51C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | chr1 | 22601576 | ||||||
chr1:22601593 | G | A | 3 | a0002c0003t0002g0075a0002c0003t0002g0084a0002c0003t0002g0092 | 3 | HG03831.hp1 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2904-34G>A | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | chr1 | 22601593 | ||||||
chr1:22601604 | C | T | 8 | a0002c0004t0011g0061a0002c0004t0011g0177a0002c0004t0011g0178others(5): Show | 10 | HG02055.hp2 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2904-23C>T | EPHA8 | ENSG00000070886.12 | transcript | ENST00000166244.8 | protein_coding | 16/16 | chr1 | 22601604 |