geneid | 58478 |
---|---|
ensemblid | ENSG00000145293.17 |
hgncid | 24599 |
symbol | ENOPH1 |
name | enolase-phosphatase 1 |
refseq_nuc | NM_021204.5 |
refseq_prot | NP_067027.1 |
ensembl_nuc | ENST00000273920.8 |
ensembl_prot | ENSP00000273920.3 |
mane_status | MANE Select |
chr | chr4 |
start | 82430590 |
end | 82461177 |
strand | + |
ver | v1.2 |
region | chr4:82430590-82461177 |
region5000 | chr4:82425590-82466177 |
regionname0 | ENOPH1_chr4_82430590_82461177 |
regionname5000 | ENOPH1_chr4_82425590_82466177 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 261 | 364 | 95 | 63 | 154 | 12 | 38 | 120 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0002 | 0/0 | 261 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 786 | 363 | 95 | 63 | 153 | 12 | 38 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
c0002 | 0/0 | 786 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
c0003 | 0/0 | 786 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1298 | 258 | 57 | 53 | 107 | 10 | 29 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0002 | 0/0 | 1298 | 28 | 4 | 3 | 13 | 1 | 7 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0003 | 0/0 | 1298 | 22 | 1 | 2 | 19 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0004 | 0/0 | 1298 | 21 | 14 | 0 | 7 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0005 | 0/0 | 1298 | 13 | 0 | 6 | 6 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0006 | 0/0 | 1298 | 11 | 11 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0007 | 0/0 | 1298 | 9 | 9 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0008 | 0/0 | 1298 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0009 | 0/0 | 1298 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
t0010 | 0/0 | 1298 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 0 | 8 | 0 | 3 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0002 | 0/0 | 7 | 0 | 1 | 3 | 0 | 3 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0029 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 786 | 363 | 95 | 63 | 153 | 12 | 38 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0003 | 0/0 | 786 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0002c0002 | 0/0 | 786 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2083 | 256 | 56 | 52 | 107 | 10 | 29 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0002 | 0/0 | 2083 | 28 | 4 | 3 | 13 | 1 | 7 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0003 | 0/0 | 2083 | 22 | 1 | 2 | 19 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0004 | 0/0 | 2083 | 21 | 14 | 0 | 7 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0005 | 0/0 | 2083 | 12 | 0 | 6 | 5 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0006 | 0/0 | 2083 | 11 | 11 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0007 | 0/0 | 2083 | 9 | 9 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0008 | 0/0 | 2083 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0009 | 0/0 | 2083 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0001t0010 | 0/0 | 2083 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0001c0003t0005 | 0/0 | 2083 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
a0002c0002t0001 | 0/0 | 2083 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | copy fasta | chr4 | 82425590 | 82466177 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 3 | 0 | 3 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0029 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0001c0003t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0085 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | IBS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0087 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0091 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0289 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0088 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | CDX | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | CDX | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0069 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0065 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03491 | hp2 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03492 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18975 | hp2 | a0001 | c0003 | t0005 | g0101 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18990 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19066 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0095 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0074 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0167 | AFR | USA | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0029 | REF | REF | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0062 | REF | REF | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82451233
|
G | A | 1 | a0002 | 2 | HG01256.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.377G>A | p.Arg126His | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/6 | 617/2083 | 377/786 | 126/261 | chr4 | 82451233 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82460042
|
A | G | 1 | a0001c0003 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.708A>G | p.Ala236Ala | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 948/2083 | 708/786 | 236/261 | chr4 | 82460042 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82430668
|
A | G | 5 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(2): Show | 61 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-162A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/6 | 162 | chr4 | 82430668 | |||||
chr4:82430692
|
G | T | 3 | a0001c0001t0002a0001c0001t0005a0001c0003t0005 | 41 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(38): Show |
5_prime_UTR_variant | MODIFIER | c.-138G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/6 | 138 | chr4 | 82430692 | |||||
chr4:82460142
|
C | T | 2 | a0001c0001t0004a0001c0001t0006 | 32 | HG01891.hp1 HG02132.hp2 HG02145.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 22 | chr4 | 82460142 | |||||
chr4:82460411
|
C | A | 3 | a0001c0001t0003a0001c0001t0005a0001c0003t0005 | 35 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*291C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 291 | chr4 | 82460411 | |||||
chr4:82460746
|
T | C | 1 | a0001c0001t0009 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*626T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 626 | chr4 | 82460746 | |||||
chr4:82460851
|
A | G | 1 | a0001c0001t0010 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 731 | chr4 | 82460851 | |||||
chr4:82461126
|
C | T | 1 | a0001c0001t0008 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1006C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 1006 | chr4 | 82461126 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:82430996
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.84+83G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82430996 | ||||||
chr4:82430997
|
A | C | 1 | a0001c0001t0001g0296 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.84+84A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82430997 | ||||||
chr4:82431024
|
C | CTT | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.84+112_84+113insTT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82431024 | |||||
chr4:82431033
|
G | C | 50 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(47): Show | 55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+120G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431033 | ||||||
chr4:82431203
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.84+290G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431203 | ||||||
chr4:82431302
|
C | T | 2 | a0001c0001t0004g0293a0001c0001t0004g0294 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.84+389C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431302 | ||||||
chr4:82431305
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.84+392C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431305 | ||||||
chr4:82431617
|
G | T | 3 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109 | 3 | HG02559.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.84+704G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431617 | ||||||
chr4:82431704
|
T | A | 14 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(11): Show | 15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+791T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431704 | ||||||
chr4:82431834
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.84+921C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431834 | ||||||
chr4:82431891
|
A | T | 15 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(12): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.84+978A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431891 | ||||||
chr4:82431915
|
C | CT | 9 | a0001c0001t0001g0064a0001c0001t0001g0284a0001c0001t0001g0285others(6): Show | 9 | HG00323.hp2 HG01192.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+1016dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82431915 | |||||
chr4:82431915
|
CT | C | 39 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0018others(36): Show | 43 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.84+1016delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82431915 | |||||
chr4:82431948
|
G | C | 2 | a0001c0001t0004g0042a0001c0001t0004g0043 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.84+1035G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431948 | ||||||
chr4:82432017
|
A | G | 37 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(34): Show | 41 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.84+1104A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432017 | ||||||
chr4:82432644
|
C | CGTTTT | 10 | a0001c0001t0001g0012a0001c0001t0001g0288a0001c0001t0002g0077others(7): Show | 13 | HG01884.hp2 HG02717.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+1756_84+1760dup others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | |||||
chr4:82432644
|
C | CGTTTTGT others(3): Show |
7 | a0001c0001t0001g0282a0001c0001t0006g0069a0001c0001t0006g0070others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+1751_84+1760dup others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | |||||
chr4:82432644
|
C | CGTTTTGT others(8): Show |
4 | a0001c0001t0001g0283a0001c0001t0002g0078a0001c0001t0002g0105others(1): Show | 4 | HG00621.hp1 HG03491.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+1746_84+1760dup others(15): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | |||||
chr4:82432644
|
C | CGTTTTGT others(13): Show |
30 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0079others(27): Show | 34 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+1741_84+1760dup others(20): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | |||||
chr4:82432688
|
T | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG03225.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.84+1775T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432688 | ||||||
chr4:82432791
|
C | A | 13 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 13 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+1878C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432791 | ||||||
chr4:82432805
|
A | G | 5 | a0001c0001t0007g0015a0001c0001t0007g0065a0001c0001t0007g0066others(2): Show | 6 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+1892A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432805 | ||||||
chr4:82432901
|
C | T | 1 | a0001c0001t0006g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+1988C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432901 | ||||||
chr4:82432985
|
CT | C | 50 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(47): Show | 55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+2081delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432985 | |||||
chr4:82433247
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.84+2334C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433247 | ||||||
chr4:82433307
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+2394G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433307 | ||||||
chr4:82433361
|
T | C | 14 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(11): Show | 15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+2448T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433361 | ||||||
chr4:82433388
|
T | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+2475T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433388 | ||||||
chr4:82433513
|
A | G | 2 | a0001c0001t0003g0040a0001c0001t0003g0280 | 3 | NA18991.hp1 NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.84+2600A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433513 | ||||||
chr4:82433682
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84+2769A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433682 | ||||||
chr4:82433742
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.84+2829C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433742 | ||||||
chr4:82433803
|
T | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+2890T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433803 | ||||||
chr4:82433868
|
T | C | 34 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0110others(31): Show | 36 | HG00558.hp2 HG00597.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+2955T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433868 | ||||||
chr4:82434185
|
G | A | 2 | a0001c0001t0004g0293a0001c0001t0004g0294 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.84+3272G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434185 | ||||||
chr4:82434348
|
C | T | 2 | a0001c0001t0004g0159a0001c0001t0004g0160 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.84+3435C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434348 | ||||||
chr4:82434474
|
G | A | 90 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 114 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.84+3561G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434474 | ||||||
chr4:82434479
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.84+3566C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434479 | ||||||
chr4:82434543
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.84+3630G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434543 | ||||||
chr4:82434571
|
G | A | 1 | a0001c0001t0004g0293 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.84+3658G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434571 | ||||||
chr4:82434721
|
G | A | 50 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(47): Show | 55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+3808G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434721 | ||||||
chr4:82434769
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84+3856T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434769 | ||||||
chr4:82434776
|
G | A | 32 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(29): Show | 36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+3863G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434776 | ||||||
chr4:82434822
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.84+3909G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434822 | ||||||
chr4:82434897
|
A | ACT | 50 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(47): Show | 55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+3985_84+3986dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82434897 | |||||
chr4:82434898
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+3985C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434898 | ||||||
chr4:82434905
|
TA | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0158a0001c0001t0001g0226others(4): Show | 7 | HG01168.hp2 HG02040.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+4006delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82434905 | |||||
chr4:82435054
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 8 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+4141C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435054 | ||||||
chr4:82435197
|
G | A | 1 | a0001c0001t0003g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.84+4284G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435197 | ||||||
chr4:82435294
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.84+4381G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435294 | ||||||
chr4:82435445
|
G | A | 14 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(11): Show | 15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+4532G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435445 | ||||||
chr4:82435535
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.84+4622A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435535 | ||||||
chr4:82435741
|
A | G | 2 | a0001c0001t0001g0278a0001c0001t0003g0277 | 2 | NA18977.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.84+4828A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435741 | ||||||
chr4:82435836
|
A | G | 14 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(11): Show | 15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+4923A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435836 | ||||||
chr4:82435846
|
A | G | 14 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(11): Show | 15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+4933A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435846 | ||||||
chr4:82435940
|
T | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(81): Show | 96 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.84+5027T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435940 | ||||||
chr4:82435944
|
A | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+5031A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435944 | ||||||
chr4:82435967
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0229 | 2 | NA18982.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.84+5054C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435967 | ||||||
chr4:82435999
|
T | A | 1 | a0001c0001t0001g0045 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.84+5086T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435999 | ||||||
chr4:82436163
|
C | T | 32 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(29): Show | 36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+5250C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436163 | ||||||
chr4:82436300
|
C | T | 1 | a0001c0001t0003g0280 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.84+5387C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436300 | ||||||
chr4:82436392
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.84+5479G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436392 | ||||||
chr4:82436483
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.84+5570C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436483 | ||||||
chr4:82436641
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.84+5728C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436641 | ||||||
chr4:82436686
|
C | CA | 33 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(30): Show | 39 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+5791dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | |||||
chr4:82436686
|
C | CAA | 9 | a0001c0001t0004g0042a0001c0001t0006g0070a0001c0001t0006g0071others(6): Show | 9 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+5790_84+5791dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | |||||
chr4:82436686
|
C | CAAA | 6 | a0001c0001t0006g0069a0001c0001t0007g0015a0001c0001t0007g0065others(3): Show | 7 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+5789_84+5791dup others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | |||||
chr4:82436686
|
CA | C | 34 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0002g0018others(31): Show | 38 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.84+5791delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | |||||
chr4:82436840
|
AGTTCCCT others(5): Show |
A | 1 | a0001c0001t0001g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.84+5928_84+5939del others(12): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436840 | ||||||
chr4:82437251
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0226others(1): Show | 4 | HG02080.hp2 NA18990.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+6338G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437251 | ||||||
chr4:82437512
|
G | A | 1 | a0001c0001t0006g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.84+6599G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437512 | ||||||
chr4:82437535
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.84+6622A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437535 | ||||||
chr4:82437609
|
T | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 34 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.84+6696T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437609 | ||||||
chr4:82437652
|
G | A | 3 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109 | 3 | HG02559.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.84+6739G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437652 | ||||||
chr4:82437826
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.84+6913A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437826 | ||||||
chr4:82437831
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0274a0001c0001t0001g0275 | 7 | HG00099.hp1 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+6918G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437831 | ||||||
chr4:82437884
|
C | T | 2 | a0001c0001t0007g0075a0001c0001t0007g0076 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.84+6971C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437884 | ||||||
chr4:82438035
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.84+7122T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438035 | ||||||
chr4:82438158
|
C | A | 1 | a0001c0001t0001g0135 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.84+7245C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438158 | ||||||
chr4:82438221
|
G | A | 2 | a0001c0001t0007g0065a0001c0001t0007g0066 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.84+7308G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438221 | ||||||
chr4:82438391
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.84+7478C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438391 | ||||||
chr4:82438420
|
A | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(71): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.84+7507A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438420 | ||||||
chr4:82438431
|
AT | A | 32 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(29): Show | 36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+7520delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82438431 | |||||
chr4:82438503
|
A | T | 1 | a0001c0001t0001g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.84+7590A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438503 | ||||||
chr4:82438505
|
T | G | 1 | a0001c0001t0001g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.84+7592T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438505 | ||||||
chr4:82438676
|
A | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0216a0001c0001t0004g0156 | 3 | HG01123.hp2 HG02027.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.84+7763A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438676 | ||||||
chr4:82438880
|
T | C | 32 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(29): Show | 36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+7967T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438880 | ||||||
chr4:82438892
|
C | T | 2 | a0001c0001t0007g0075a0001c0001t0007g0076 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.84+7979C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438892 | ||||||
chr4:82438999
|
C | T | 14 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(11): Show | 15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+8086C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438999 | ||||||
chr4:82439033
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.84+8120A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439033 | ||||||
chr4:82439051
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0004g0156 | 2 | HG01123.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.84+8138C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439051 | ||||||
chr4:82439054
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.84+8141G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439054 | ||||||
chr4:82439086
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.84+8173C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439086 | ||||||
chr4:82439305
|
C | T | 2 | a0001c0001t0007g0075a0001c0001t0007g0076 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.84+8392C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439305 | ||||||
chr4:82439631
|
A | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-8289A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439631 | ||||||
chr4:82439785
|
T | C | 2 | a0001c0001t0006g0020a0001c0001t0007g0289 | 3 | HG02055.hp1 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.85-8135T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439785 | ||||||
chr4:82439892
|
G | C | 1 | a0001c0001t0001g0023 | 2 | NA18941.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.85-8028G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439892 | ||||||
chr4:82440430
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.85-7490G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440430 | ||||||
chr4:82440477
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.85-7443C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440477 | ||||||
chr4:82440762
|
ATAATT | A | 5 | a0001c0001t0007g0015a0001c0001t0007g0065a0001c0001t0007g0066others(2): Show | 6 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-7153_85-7149del others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82440762 | |||||
chr4:82440784
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.85-7136G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440784 | ||||||
chr4:82440980
|
A | G | 14 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(11): Show | 14 | HG02258.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-6940A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440980 | ||||||
chr4:82440984
|
A | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.85-6936A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440984 | ||||||
chr4:82441039
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(82): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.85-6881A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441039 | ||||||
chr4:82441091
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-6829G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441091 | ||||||
chr4:82441210
|
C | T | 30 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(27): Show | 35 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.85-6710C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441210 | ||||||
chr4:82441303
|
C | T | 5 | a0001c0001t0004g0293a0001c0001t0004g0294a0001c0001t0006g0107others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-6617C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441303 | ||||||
chr4:82441360
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0285a0001c0001t0004g0136others(3): Show | 6 | HG02132.hp2 HG02165.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-6560T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441360 | ||||||
chr4:82441371
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.85-6549C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441371 | ||||||
chr4:82441405
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.85-6515G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441405 | ||||||
chr4:82441431
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0233a0001c0001t0001g0237 | 3 | HG01891.hp2 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.85-6489T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441431 | ||||||
chr4:82441432
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0233a0001c0001t0001g0237 | 3 | HG01891.hp2 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.85-6488T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441432 | ||||||
chr4:82441549
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.85-6371A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441549 | ||||||
chr4:82441591
|
G | A | 1 | a0001c0001t0003g0166 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.85-6329G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441591 | ||||||
chr4:82441637
|
A | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(27): Show | 36 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.85-6283A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441637 | ||||||
chr4:82441653
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.85-6267T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441653 | ||||||
chr4:82441715
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-6205G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441715 | ||||||
chr4:82441764
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.85-6156A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441764 | ||||||
chr4:82441776
|
AAAAC | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0033others(19): Show | 26 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.85-6141_85-6138del others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82441776 | |||||
chr4:82441777
|
A | AAAC | 6 | a0001c0001t0001g0157a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG00140.hp1 HG01123.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-6125_85-6123dup others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82441777 | |||||
chr4:82441801
|
T | C | 2 | a0001c0001t0005g0016a0001c0001t0005g0081 | 3 | HG00609.hp1 NA18960.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.85-6119T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441801 | ||||||
chr4:82441922
|
T | A | 6 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-5998T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441922 | ||||||
chr4:82442137
|
T | G | 4 | a0001c0001t0002g0078a0001c0001t0002g0082a0001c0001t0002g0084others(1): Show | 4 | HG00438.hp2 HG00621.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-5783T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442137 | ||||||
chr4:82442184
|
A | G | 28 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(25): Show | 33 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.85-5736A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442184 | ||||||
chr4:82442268
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(28): Show | 36 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.85-5652C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442268 | ||||||
chr4:82442306
|
G | C | 6 | a0001c0001t0001g0133a0001c0001t0001g0141a0001c0001t0004g0142others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-5614G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442306 | ||||||
chr4:82442420
|
C | T | 33 | a0001c0001t0001g0153a0001c0001t0001g0273a0001c0001t0002g0018others(30): Show | 37 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-5500C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442420 | ||||||
chr4:82442475
|
G | A | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0007g0015others(4): Show | 8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-5445G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442475 | ||||||
chr4:82442531
|
CAA | C | 8 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0006g0069others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-5382_85-5381del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442531 | |||||
chr4:82442547
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0060others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-5373G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442547 | ||||||
chr4:82442558
|
A | AT | 14 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(11): Show | 14 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-5352dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442558 | |||||
chr4:82442558
|
AT | A | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-5352delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442558 | |||||
chr4:82442629
|
A | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-5291A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442629 | ||||||
chr4:82442734
|
C | T | 14 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(11): Show | 14 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-5186C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442734 | ||||||
chr4:82442864
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 8 | HG02083.hp2 NA18945.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-5056G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442864 | ||||||
chr4:82442931
|
T | TCTCATGT others(3): Show |
1 | a0001c0001t0001g0238 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.85-4988_85-4979dup others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442931 | |||||
chr4:82442998
|
G | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0059others(28): Show | 33 | HG00323.hp2 HG01167.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.85-4922G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442998 | ||||||
chr4:82443071
|
G | A | 2 | a0001c0001t0004g0042a0001c0001t0004g0043 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.85-4849G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443071 | ||||||
chr4:82443094
|
C | T | 1 | a0001c0001t0006g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85-4826C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443094 | ||||||
chr4:82443100
|
C | T | 2 | a0001c0001t0004g0159a0001c0001t0004g0160 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.85-4820C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443100 | ||||||
chr4:82443243
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.85-4677C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443243 | ||||||
chr4:82443369
|
C | T | 1 | a0001c0001t0006g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-4551C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443369 | ||||||
chr4:82443410
|
C | CA | 30 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0117others(27): Show | 32 | HG00323.hp2 HG01167.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.85-4500dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443410 | |||||
chr4:82443525
|
G | A | 1 | a0001c0001t0004g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.85-4395G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443525 | ||||||
chr4:82443528
|
G | A | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4392G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443528 | ||||||
chr4:82443538
|
T | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4382T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443538 | ||||||
chr4:82443544
|
T | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4376T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443544 | ||||||
chr4:82443570
|
C | T | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4350C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443570 | ||||||
chr4:82443581
|
G | A | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4339G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443581 | ||||||
chr4:82443588
|
C | T | 6 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-4332C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443588 | ||||||
chr4:82443594
|
G | A | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4326G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443594 | ||||||
chr4:82443596
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.85-4324C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443596 | ||||||
chr4:82443606
|
A | T | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4314A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443606 | ||||||
chr4:82443618
|
C | T | 1 | a0001c0001t0006g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.85-4302C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443618 | ||||||
chr4:82443638
|
A | G | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4282A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443638 | ||||||
chr4:82443645
|
A | G | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4275A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443645 | ||||||
chr4:82443653
|
A | G | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4267A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443653 | ||||||
chr4:82443655
|
C | G | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4265C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443655 | ||||||
chr4:82443659
|
T | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4261T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443659 | ||||||
chr4:82443676
|
T | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4244T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443676 | ||||||
chr4:82443682
|
T | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4238T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443682 | ||||||
chr4:82443684
|
T | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4236T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443684 | ||||||
chr4:82443693
|
C | A | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4227C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443693 | ||||||
chr4:82443704
|
G | GGC | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4215_85-4214ins others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443704 | |||||
chr4:82443712
|
T | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4208T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443712 | ||||||
chr4:82443718
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0131others(4): Show | 7 | HG01167.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-4202T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443718 | ||||||
chr4:82443720
|
CA | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4199delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443720 | ||||||
chr4:82443726
|
C | CAAAAAAA others(7): Show |
24 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(21): Show | 27 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.85-4184_85-4183ins others(14): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443726 | |||||
chr4:82443726
|
C | CAAAAAAA others(8): Show |
9 | a0001c0001t0002g0079a0001c0001t0002g0089a0001c0001t0002g0090others(6): Show | 10 | HG01109.hp2 HG01175.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-4184_85-4183ins others(15): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443726 | |||||
chr4:82443771
|
GTTTAA | G | 6 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0205others(3): Show | 6 | NA18939.hp1 NA18939.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-4145_85-4141del others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443771 | |||||
chr4:82443827
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.85-4093T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443827 | ||||||
chr4:82444007
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85-3913C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444007 | ||||||
chr4:82444225
|
C | CT | 43 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(40): Show | 47 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.85-3681dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82444225 | |||||
chr4:82444243
|
A | G | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0007g0015others(4): Show | 8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-3677A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444243 | ||||||
chr4:82444335
|
T | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(96): Show | 111 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.85-3585T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444335 | ||||||
chr4:82444438
|
C | T | 23 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0117others(20): Show | 24 | HG01167.hp2 HG02055.hp1 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.85-3482C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444438 | ||||||
chr4:82444447
|
A | G | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-3473A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444447 | ||||||
chr4:82444501
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(63): Show | 75 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.85-3419C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444501 | ||||||
chr4:82444563
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-3357G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444563 | ||||||
chr4:82444602
|
G | C | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-3318G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444602 | ||||||
chr4:82444645
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85-3275A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444645 | ||||||
chr4:82444833
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0269 | 6 | HG01255.hp2 HG01346.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-3087A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444833 | ||||||
chr4:82445155
|
G | T | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0007g0015others(4): Show | 8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-2765G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445155 | ||||||
chr4:82445215
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.85-2705C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445215 | ||||||
chr4:82445235
|
GA | G | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-2675delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82445235 | |||||
chr4:82445307
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85-2613T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445307 | ||||||
chr4:82445485
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(63): Show | 75 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.85-2435C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445485 | ||||||
chr4:82445520
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.85-2400A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445520 | ||||||
chr4:82445678
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.85-2242A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445678 | ||||||
chr4:82445876
|
A | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0276 | 2 | HG00408.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.85-2044A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445876 | ||||||
chr4:82445930
|
C | T | 41 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(38): Show | 45 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.85-1990C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445930 | ||||||
chr4:82446156
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1764G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446156 | ||||||
chr4:82446190
|
G | A | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-1730G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446190 | ||||||
chr4:82446413
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-1507C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446413 | ||||||
chr4:82446421
|
C | CA | 50 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(47): Show | 54 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.85-1487dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446421 | |||||
chr4:82446421
|
C | CAA | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1488_85-1487dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446421 | |||||
chr4:82446467
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.85-1453C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446467 | ||||||
chr4:82446662
|
C | CT | 69 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0117others(66): Show | 74 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.85-1244dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446662 | |||||
chr4:82446662
|
C | CTT | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1245_85-1244dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446662 | |||||
chr4:82446673
|
T | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0285a0001c0001t0003g0040others(1): Show | 5 | HG02027.hp2 NA18954.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-1247T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446673 | ||||||
chr4:82446675
|
T | G | 21 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0030others(18): Show | 25 | HG00438.hp1 HG00735.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.85-1245T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446675 | ||||||
chr4:82446676
|
TG | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0133others(27): Show | 32 | HG00140.hp2 HG00597.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.85-1243delG | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446676 | ||||||
chr4:82446677
|
G | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.85-1243G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446677 | ||||||
chr4:82446683
|
C | G | 1 | a0001c0001t0004g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.85-1237C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446683 | ||||||
chr4:82446689
|
C | CT | 69 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(66): Show | 82 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.85-1203dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | |||||
chr4:82446689
|
CT | C | 11 | a0001c0001t0001g0292a0001c0001t0002g0077a0001c0001t0002g0078others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-1203delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | |||||
chr4:82446689
|
CTT | C | 22 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0080others(19): Show | 26 | HG00558.hp1 HG00609.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.85-1204_85-1203del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | |||||
chr4:82446689
|
CTTTTTTT others(1): Show |
C | 29 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0117others(26): Show | 31 | HG00323.hp2 HG01167.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.85-1210_85-1203del others(8): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | |||||
chr4:82446689
|
CTTTTTTT others(7): Show |
C | 8 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0006g0069others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-1216_85-1203del others(14): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | |||||
chr4:82446689
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0014a0001c0001t0001g0055 | 3 | HG02809.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.85-1217_85-1203del others(15): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | |||||
chr4:82446689
|
CTTTTTTT others(9): Show |
C | 23 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 27 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.85-1218_85-1203del others(16): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | |||||
chr4:82446721
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.85-1199A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446721 | ||||||
chr4:82446722
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-1198C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446722 | ||||||
chr4:82446747
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.85-1173C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446747 | ||||||
chr4:82446778
|
C | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1142C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446778 | ||||||
chr4:82446792
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.85-1128C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446792 | ||||||
chr4:82446831
|
C | T | 1 | a0001c0001t0005g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.85-1089C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446831 | ||||||
chr4:82446852
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.85-1068G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446852 | ||||||
chr4:82446861
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1059C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446861 | ||||||
chr4:82446868
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0256 | 3 | HG02896.hp2 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.85-1052G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446868 | ||||||
chr4:82446875
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0256 | 3 | HG02896.hp2 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.85-1045T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446875 | ||||||
chr4:82446928
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-992G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446928 | ||||||
chr4:82446969
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.85-951G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446969 | ||||||
chr4:82447237
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.85-683C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447237 | ||||||
chr4:82447335
|
A | G | 1 | a0001c0001t0007g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.85-585A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447335 | ||||||
chr4:82447353
|
GTTTGT | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0131others(4): Show | 7 | HG01167.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-558_85-554delGT others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82447353 | |||||
chr4:82447464
|
G | A | 33 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(30): Show | 37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-456G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447464 | ||||||
chr4:82447573
|
C | T | 6 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-347C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447573 | ||||||
chr4:82447827
|
T | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(22): Show | 30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-93T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447827 | ||||||
chr4:82448134
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.186+113A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448134 | ||||||
chr4:82448223
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186+202T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448223 | ||||||
chr4:82448236
|
G | GT | 5 | a0001c0001t0001g0162a0001c0001t0007g0015a0001c0001t0007g0065others(2): Show | 6 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+224dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448236 | |||||
chr4:82448241
|
TTTTTGTT others(3): Show |
T | 1 | a0001c0003t0005g0101 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.186+235_186+244del others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448241 | |||||
chr4:82448251
|
GTTTTGTT others(7): Show |
G | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0002c0002t0001g0167 | 3 | HG00323.hp2 HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.186+240_186+253del others(14): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448251 | |||||
chr4:82448260
|
TG | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0054 | 7 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+240delG | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448260 | ||||||
chr4:82448266
|
T | G | 1 | a0002c0002t0001g0144 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.186+245T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448266 | ||||||
chr4:82448270
|
G | GT | 18 | a0001c0001t0001g0130a0001c0001t0001g0157a0001c0001t0001g0190others(15): Show | 18 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.186+258dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448270 | |||||
chr4:82448271
|
T | G | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.186+250T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448271 | ||||||
chr4:82448346
|
C | A | 6 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+325C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448346 | ||||||
chr4:82448507
|
C | A | 1 | a0001c0001t0001g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.186+486C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448507 | ||||||
chr4:82448545
|
A | C | 3 | a0001c0001t0004g0047a0001c0001t0004g0048a0001c0001t0004g0061 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.186+524A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448545 | ||||||
chr4:82448715
|
A | G | 41 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0077others(38): Show | 45 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.186+694A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448715 | ||||||
chr4:82448728
|
C | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 27 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.186+707C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448728 | ||||||
chr4:82448860
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.186+839C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448860 | ||||||
chr4:82448864
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.186+843T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448864 | ||||||
chr4:82449057
|
C | CA | 9 | a0001c0001t0001g0224a0001c0001t0002g0077a0001c0001t0002g0078others(6): Show | 9 | HG00621.hp1 HG01175.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+1060dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | |||||
chr4:82449057
|
CA | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(144): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.186+1060delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | |||||
chr4:82449057
|
CAA | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(66): Show | 75 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.186+1059_186+1060d others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | |||||
chr4:82449057
|
CAAA | C | 22 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0059others(19): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.186+1058_186+1060d others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | |||||
chr4:82449057
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0014a0001c0001t0001g0055 | 3 | HG02809.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.186+1051_186+1060d others(12): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | |||||
chr4:82449189
|
G | A | 16 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0117others(13): Show | 16 | HG01167.hp2 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+1168G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449189 | ||||||
chr4:82449212
|
C | T | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0007g0015others(4): Show | 8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+1191C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449212 | ||||||
chr4:82449274
|
A | G | 6 | a0001c0001t0006g0069a0001c0001t0006g0070a0001c0001t0006g0071others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+1253A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449274 | ||||||
chr4:82449421
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.186+1400C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449421 | ||||||
chr4:82449478
|
C | T | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0002c0002t0001g0167 | 3 | HG00323.hp2 HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.186+1457C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449478 | ||||||
chr4:82449536
|
T | C | 31 | a0001c0001t0001g0257a0001c0001t0002g0018a0001c0001t0002g0019others(28): Show | 35 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.187-1507T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449536 | ||||||
chr4:82449569
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.187-1474T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449569 | ||||||
chr4:82449658
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0055 | 3 | HG02809.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.187-1385T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449658 | ||||||
chr4:82449681
|
A | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0044others(26): Show | 34 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.187-1362A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449681 | ||||||
chr4:82449763
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187-1280T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449763 | ||||||
chr4:82449764
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187-1279C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449764 | ||||||
chr4:82449788
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.187-1255C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449788 | ||||||
chr4:82449942
|
A | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0133others(35): Show | 40 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.187-1101A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449942 | ||||||
chr4:82450144
|
T | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0241 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.187-899T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450144 | ||||||
chr4:82450163
|
G | A | 41 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0052others(38): Show | 44 | HG00140.hp2 HG00597.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.187-880G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450163 | ||||||
chr4:82450192
|
G | T | 8 | a0001c0001t0001g0013a0001c0001t0003g0243a0001c0001t0004g0159others(5): Show | 9 | HG02145.hp2 HG02559.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.187-851G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450192 | ||||||
chr4:82450234
|
T | C | 28 | a0001c0001t0001g0035a0001c0001t0001g0131a0001c0001t0001g0225others(25): Show | 32 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.187-809T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450234 | ||||||
chr4:82450244
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.187-799C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450244 | ||||||
chr4:82450323
|
G | A | 6 | a0001c0001t0001g0151a0001c0001t0001g0246a0001c0001t0004g0136others(3): Show | 6 | HG02132.hp2 HG02165.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-720G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450323 | ||||||
chr4:82450431
|
T | C | 1 | a0001c0001t0005g0094 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.187-612T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450431 | ||||||
chr4:82451318
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.389+73T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451318 | ||||||
chr4:82451492
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.389+247G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451492 | ||||||
chr4:82451812
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.389+567G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451812 | ||||||
chr4:82451815
|
C | G | 20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(17): Show | 24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+570C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451815 | ||||||
chr4:82451903
|
C | T | 12 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0038others(9): Show | 15 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.389+658C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451903 | ||||||
chr4:82451960
|
TAGTAC | T | 20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(17): Show | 24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+718_389+722del others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82451960 | |||||
chr4:82452015
|
G | C | 20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(17): Show | 24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+770G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452015 | ||||||
chr4:82452061
|
G | A | 3 | a0001c0001t0007g0015a0001c0001t0007g0067a0001c0001t0007g0068 | 4 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.389+816G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452061 | ||||||
chr4:82452082
|
AT | A | 20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(17): Show | 24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+850delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452082 | |||||
chr4:82452104
|
G | T | 6 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0048others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.389+859G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452104 | ||||||
chr4:82452334
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+1089G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452334 | ||||||
chr4:82452383
|
A | G | 20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(17): Show | 24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+1138A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452383 | ||||||
chr4:82452479
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.389+1234A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452479 | ||||||
chr4:82452516
|
T | C | 33 | a0001c0001t0001g0051a0001c0001t0002g0112a0001c0001t0002g0114others(30): Show | 38 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.389+1271T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452516 | ||||||
chr4:82452594
|
A | G | 65 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(62): Show | 76 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(73): Show |
intron_variant | MODIFIER | c.389+1349A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452594 | ||||||
chr4:82452707
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.389+1462C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452707 | ||||||
chr4:82452775
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0002g0100 | 2 | HG02015.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.389+1530C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452775 | ||||||
chr4:82452869
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.389+1624T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452869 | ||||||
chr4:82452877
|
T | C | 104 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(101): Show | 117 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.389+1632T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452877 | ||||||
chr4:82452885
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+1640G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452885 | ||||||
chr4:82452900
|
C | CT | 10 | a0001c0001t0001g0046a0001c0001t0001g0064a0001c0001t0001g0134others(7): Show | 10 | HG01243.hp1 HG02015.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+1674dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452900 | |||||
chr4:82452900
|
CT | C | 6 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0180others(3): Show | 6 | HG02451.hp2 HG02723.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+1674delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452900 | |||||
chr4:82452918
|
T | C | 29 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(26): Show | 34 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.389+1673T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452918 | ||||||
chr4:82452918
|
T | TC | 62 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0055others(59): Show | 69 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.389+1673_389+1674i others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452918 | ||||||
chr4:82452918
|
T | TTC | 13 | a0001c0001t0003g0161a0001c0001t0004g0042a0001c0001t0004g0043others(10): Show | 14 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+1674_389+1675i others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452918 | |||||
chr4:82452994
|
T | C | 2 | a0001c0001t0005g0016a0001c0001t0005g0081 | 3 | HG00609.hp1 NA18960.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.390-1728T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452994 | ||||||
chr4:82453059
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.390-1663G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453059 | ||||||
chr4:82453059
|
G | T | 6 | a0001c0001t0003g0026a0001c0001t0003g0166a0001c0001t0003g0183others(3): Show | 7 | HG00423.hp1 HG01109.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-1663G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453059 | ||||||
chr4:82453118
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.390-1604C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453118 | ||||||
chr4:82453118
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390-1604C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453118 | ||||||
chr4:82453178
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0219 | 2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.390-1544A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453178 | ||||||
chr4:82453316
|
T | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(14): Show | 24 | HG01106.hp1 HG01123.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.390-1406T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453316 | ||||||
chr4:82453320
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-1402T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453320 | ||||||
chr4:82453598
|
T | C | 1 | a0001c0001t0006g0020 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.390-1124T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453598 | ||||||
chr4:82453636
|
A | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 5 | HG02809.hp2 HG03209.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.390-1086A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453636 | ||||||
chr4:82453695
|
T | A | 10 | a0001c0001t0001g0126a0001c0001t0001g0141a0001c0001t0001g0195others(7): Show | 11 | HG00323.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.390-1027T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453695 | ||||||
chr4:82453732
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.390-990C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453732 | ||||||
chr4:82453884
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.390-838A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453884 | ||||||
chr4:82454050
|
TA | T | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.390-655delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82454050 | |||||
chr4:82454050
|
TAA | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0133others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-656_390-655del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82454050 | |||||
chr4:82454178
|
C | T | 10 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0047others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-544C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454178 | ||||||
chr4:82454257
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-465C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454257 | ||||||
chr4:82454258
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-464T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454258 | ||||||
chr4:82454259
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-463T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454259 | ||||||
chr4:82454260
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-462T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454260 | ||||||
chr4:82454261
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-461G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454261 | ||||||
chr4:82454262
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-460A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454262 | ||||||
chr4:82454263
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-459G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454263 | ||||||
chr4:82454265
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-457C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454265 | ||||||
chr4:82454266
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-456T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454266 | ||||||
chr4:82454270
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-452A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454270 | ||||||
chr4:82454272
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-450C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454272 | ||||||
chr4:82454273
|
T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0115others(4): Show | 8 | HG02886.hp1 HG03130.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-449T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454273 | ||||||
chr4:82454291
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.390-431G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454291 | ||||||
chr4:82454566
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.390-156T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454566 | ||||||
chr4:82454593
|
G | A | 20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(17): Show | 24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.390-129G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454593 | ||||||
chr4:82454945
|
CT | C | 36 | a0001c0001t0001g0051a0001c0001t0001g0270a0001c0001t0003g0026others(33): Show | 41 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.522+103delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82454945 | |||||
chr4:82454995
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.522+141T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82454995 | ||||||
chr4:82455149
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.522+295C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455149 | ||||||
chr4:82455503
|
G | A | 10 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0047others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+649G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455503 | ||||||
chr4:82455528
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.522+674T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455528 | ||||||
chr4:82455556
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.522+702G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455556 | ||||||
chr4:82455596
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.522+742T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455596 | ||||||
chr4:82455608
|
G | A | 1 | a0001c0001t0006g0020 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.522+754G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455608 | ||||||
chr4:82455624
|
CA | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 256 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.522+782delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82455624 | |||||
chr4:82455626
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.522+772A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455626 | ||||||
chr4:82455647
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.522+793G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455647 | ||||||
chr4:82455741
|
G | A | 6 | a0001c0001t0004g0047a0001c0001t0004g0048a0001c0001t0004g0061others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+887G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455741 | ||||||
chr4:82455785
|
C | CA | 7 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0217others(4): Show | 10 | HG01123.hp1 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+944dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82455785 | |||||
chr4:82455817
|
C | A | 6 | a0001c0001t0004g0047a0001c0001t0004g0048a0001c0001t0004g0061others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+963C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455817 | ||||||
chr4:82456054
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.523-861C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456054 | ||||||
chr4:82456178
|
A | AT | 9 | a0001c0001t0001g0141a0001c0001t0001g0154a0001c0001t0001g0195others(6): Show | 10 | HG00323.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-736dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82456178 | |||||
chr4:82456215
|
CT | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.523-684delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82456215 | |||||
chr4:82456215
|
CTT | C | 8 | a0001c0001t0001g0051a0001c0001t0001g0119a0001c0001t0001g0124others(5): Show | 9 | HG02145.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.523-685_523-684del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82456215 | |||||
chr4:82456257
|
T | G | 1 | a0001c0001t0001g0197 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.523-658T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456257 | ||||||
chr4:82456353
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.523-562A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456353 | ||||||
chr4:82456527
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 8 | HG02809.hp2 HG02886.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.523-388C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456527 | ||||||
chr4:82456528
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.523-387G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456528 | ||||||
chr4:82456768
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.523-147A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456768 | ||||||
chr4:82456866
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0129others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-49G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456866 | ||||||
chr4:82457432
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.646+394T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457432 | ||||||
chr4:82457480
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(11): Show | 20 | HG01106.hp1 HG01123.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.646+442C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457480 | ||||||
chr4:82457530
|
T | C | 8 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0060others(5): Show | 9 | HG01167.hp1 HG01515.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.646+492T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457530 | ||||||
chr4:82457571
|
C | T | 2 | a0001c0001t0004g0047a0001c0001t0004g0061 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.646+533C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457571 | ||||||
chr4:82457618
|
T | TAC | 6 | a0001c0001t0004g0047a0001c0001t0004g0048a0001c0001t0004g0061others(3): Show | 7 | HG02145.hp2 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.646+595_646+596dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82457618 | |||||
chr4:82457618
|
T | TACAC | 5 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0122others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.646+593_646+596dup others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82457618 | |||||
chr4:82457719
|
G | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.646+681G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457719 | ||||||
chr4:82457755
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.646+717G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457755 | ||||||
chr4:82457768
|
T | C | 17 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(14): Show | 24 | HG01106.hp1 HG01123.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.646+730T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457768 | ||||||
chr4:82457777
|
C | T | 4 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0122others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+739C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457777 | ||||||
chr4:82458009
|
C | T | 6 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0129others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.646+971C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458009 | ||||||
chr4:82458073
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.646+1035A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458073 | ||||||
chr4:82458077
|
A | AGGCGGTG others(1): Show |
178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.646+1042_646+1043i others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82458077 | |||||
chr4:82458249
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.646+1211A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458249 | ||||||
chr4:82458380
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.646+1342G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458380 | ||||||
chr4:82458489
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.646+1451G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458489 | ||||||
chr4:82458650
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.647-1331G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458650 | ||||||
chr4:82458659
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.647-1322C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458659 | ||||||
chr4:82458673
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.647-1308T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458673 | ||||||
chr4:82458914
|
TGAG | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 8 | HG02809.hp2 HG02886.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.647-1062_647-1060d others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82458914 | |||||
chr4:82458948
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.647-1033C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458948 | ||||||
chr4:82459061
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.647-920C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459061 | ||||||
chr4:82459087
|
A | G | 3 | a0001c0001t0001g0231a0001c0001t0002g0092a0001c0001t0002g0097 | 3 | HG01361.hp2 HG02055.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.647-894A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459087 | ||||||
chr4:82459148
|
C | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0193others(4): Show | 10 | HG00597.hp2 HG02015.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.647-833C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459148 | ||||||
chr4:82459512
|
C | T | 1 | a0001c0001t0006g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.647-469C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459512 | ||||||
chr4:82459655
|
A | G | 11 | a0001c0001t0001g0126a0001c0001t0001g0141a0001c0001t0001g0154others(8): Show | 12 | HG00323.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.647-326A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459655 | ||||||
chr4:82459728
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.647-253G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459728 | ||||||
chr4:82459757
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.647-224C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459757 | ||||||
chr4:82459803
|
C | CTTT | 4 | a0001c0001t0001g0249a0001c0001t0001g0266a0001c0001t0001g0276others(1): Show | 4 | HG00408.hp2 HG02015.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-178_647-177ins others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459803 | ||||||
chr4:82459804
|
A | T | 4 | a0001c0001t0001g0249a0001c0001t0001g0266a0001c0001t0001g0276others(1): Show | 4 | HG00408.hp2 HG02015.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-177A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459804 | ||||||
chr4:82459916
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G | A | 1 | a0001c0001t0006g0071 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.647-65G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459916 |