geneid | 55840 |
---|---|
ensemblid | ENSG00000145088.9 |
hgncid | 23115 |
symbol | EAF2 |
name | ELL associated factor 2 |
refseq_nuc | NM_018456.6 |
refseq_prot | NP_060926.2 |
ensembl_nuc | ENST00000273668.7 |
ensembl_prot | ENSP00000273668.2 |
mane_status | MANE Select |
chr | chr3 |
start | 121835209 |
end | 121886526 |
strand | + |
ver | v1.2 |
region | chr3:121835209-121886526 |
region5000 | chr3:121830209-121891526 |
regionname0 | EAF2_chr3_121835209_121886526 |
regionname5000 | EAF2_chr3_121830209_121891526 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 260 | 311 | 82 | 72 | 103 | 14 | 38 | 73 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0002 | 0/0 | 260 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0003 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0004 | 0/0 | 260 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 783 | 223 | 65 | 57 | 55 | 14 | 30 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
c0002 | 0/0 | 783 | 84 | 14 | 15 | 48 | 0 | 7 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
c0003 | 0/0 | 783 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
c0004 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
c0005 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
c0006 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
c0007 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
c0008 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 216 | 316 | 86 | 72 | 106 | 13 | 37 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
t0002 | 0/0 | 216 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
t0003 | 0/0 | 216 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 0 | 9 | 0 | 3 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0002 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 783 | 223 | 65 | 57 | 55 | 14 | 30 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0002 | 0/0 | 783 | 84 | 14 | 15 | 48 | 0 | 7 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0004 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0007 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0008 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0002c0003 | 0/0 | 783 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0003c0005 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0004c0006 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 998 | 221 | 65 | 57 | 55 | 13 | 29 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0001t0002 | 0/0 | 998 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0001t0003 | 0/0 | 998 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0002t0001 | 0/0 | 998 | 84 | 14 | 15 | 48 | 0 | 7 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0004t0001 | 0/0 | 998 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0007t0001 | 0/0 | 998 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0001c0008t0001 | 0/0 | 998 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0002c0003t0001 | 0/0 | 998 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0003c0005t0001 | 0/0 | 998 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
a0004c0006t0001 | 0/0 | 998 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | copy fasta | chr3 | 121830209 | 121891526 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0001 | 0/0 | 12 | 0 | 0 | 9 | 0 | 3 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0004t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0007t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0001c0008t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0003c0005t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
a0004c0006t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0237 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02027 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02074 | hp1 | a0002 | c0003 | t0001 | g0206 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02257 | hp1 | a0003 | c0005 | t0001 | g0029 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02965 | hp2 | a0004 | c0006 | t0001 | g0030 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03041 | hp2 | a0001 | c0008 | t0001 | g0185 | AFR | GWD | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03139 | hp2 | a0004 | c0006 | t0001 | g0030 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04199 | hp2 | a0001 | c0007 | t0001 | g0200 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | STU | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | CHB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18997 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | GIH | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02486 | hp1 | a0003 | c0005 | t0001 | g0029 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | ACB | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | MSL | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | USA | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0167 | REF | REF | EAF2_chr3_121830209_121891526 | EAF2 | chr3 | 121830209 | 121891526 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835362
|
A | G | 1 | a0004 | 2 | HG02965.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.77A>G | p.Gln26Arg | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 154/998 | 77/783 | 26/260 | chr3 | 121835362 | ||
chr3:121872672
|
C | T | 1 | a0002 | 3 | HG02027.hp2 HG02074.hp1 NA18997.hp1 |
missense_variant | MODERATE | c.620C>T | p.Ser207Phe | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/6 | 697/998 | 620/783 | 207/260 | chr3 | 121872672 | ||
chr3:121872760
|
C | G | 1 | a0003 | 2 | HG02257.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.708C>G | p.Asp236Glu | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/6 | 785/998 | 708/783 | 236/260 | chr3 | 121872760 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835300
|
G | A | 1 | a0001c0007 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.15G>A | p.Ala5Ala | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 92/998 | 15/783 | 5/260 | chr3 | 121835300 | ||
chr3:121844508
|
T | C | 1 | a0001c0002 | 84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
synonymous_variant | LOW | c.162T>C | p.Gly54Gly | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/6 | 239/998 | 162/783 | 54/260 | chr3 | 121844508 | ||
chr3:121854815
|
A | G | 1 | a0001c0008 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.330A>G | p.Lys110Lys | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/6 | 407/998 | 330/783 | 110/260 | chr3 | 121854815 | ||
chr3:121872769
|
C | A | 1 | a0001c0004 | 2 | HG02145.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.717C>A | p.Gly239Gly | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/6 | 794/998 | 717/783 | 239/260 | chr3 | 121872769 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835209
|
A | T | 1 | a0001c0001t0003 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 77 | chr3 | 121835209 | |||||
chr3:121835255
|
G | A | 1 | a0001c0001t0002 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/6 | 31 | chr3 | 121835255 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:121835482
|
C | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.106+91C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121835482 | ||||||
chr3:121835752
|
G | T | 1 | a0001c0001t0003g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.106+361G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121835752 | ||||||
chr3:121836133
|
T | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(2): Show | 7 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+742T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836133 | ||||||
chr3:121836336
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.106+945T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836336 | ||||||
chr3:121836536
|
G | A | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.106+1145G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836536 | ||||||
chr3:121836599
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.106+1208C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836599 | ||||||
chr3:121836934
|
A | G | 1 | a0001c0002t0001g0250 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.106+1543A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121836934 | ||||||
chr3:121837026
|
T | C | 6 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074others(3): Show | 6 | HG01952.hp1 NA18947.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+1635T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837026 | ||||||
chr3:121837049
|
TAAAC | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.106+1662_106+1665d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121837049 | |||||
chr3:121837160
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.106+1769C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837160 | ||||||
chr3:121837372
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.106+1981C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837372 | ||||||
chr3:121837426
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(1): Show | 6 | HG02258.hp2 HG02559.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+2035G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837426 | ||||||
chr3:121837496
|
A | G | 1 | a0001c0002t0001g0249 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.106+2105A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837496 | ||||||
chr3:121837623
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.106+2232A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837623 | ||||||
chr3:121837882
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.106+2491A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837882 | ||||||
chr3:121837904
|
G | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 36 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.106+2513G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121837904 | ||||||
chr3:121838052
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.106+2661G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838052 | ||||||
chr3:121838381
|
C | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.106+2990C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838381 | ||||||
chr3:121838404
|
A | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.106+3013A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838404 | ||||||
chr3:121838686
|
G | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.106+3295G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838686 | ||||||
chr3:121838859
|
A | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0247others(1): Show | 6 | HG01981.hp1 NA18957.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+3468A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838859 | ||||||
chr3:121838877
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.106+3486G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121838877 | ||||||
chr3:121839101
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106+3710A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839101 | ||||||
chr3:121839268
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.106+3877A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839268 | ||||||
chr3:121839290
|
G | T | 1 | a0001c0002t0001g0186 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.106+3899G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839290 | ||||||
chr3:121839499
|
G | A | 2 | a0001c0002t0001g0110a0001c0002t0001g0111 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.106+4108G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839499 | ||||||
chr3:121839925
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.107-4528G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121839925 | ||||||
chr3:121840047
|
G | GC | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.107-4405dupC | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840047 | |||||
chr3:121840064
|
A | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.107-4389A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840064 | ||||||
chr3:121840189
|
G | GA | 16 | a0001c0001t0001g0024a0001c0001t0001g0069a0001c0001t0001g0071others(13): Show | 17 | HG00597.hp1 HG00642.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.107-4242dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840189 | |||||
chr3:121840189
|
GA | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(52): Show | 67 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.107-4242delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840189 | |||||
chr3:121840189
|
GAA | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 97 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.107-4243_107-4242d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840189 | |||||
chr3:121840319
|
C | A | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-4134C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840319 | ||||||
chr3:121840320
|
G | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-4133G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840320 | ||||||
chr3:121840413
|
C | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG02622.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.107-4040C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840413 | ||||||
chr3:121840428
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.107-4025T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840428 | ||||||
chr3:121840488
|
T | TA | 12 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0112others(9): Show | 16 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.107-3945dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | |||||
chr3:121840488
|
T | TAAAAAAA others(3): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0195 | 3 | HG01074.hp1 HG02922.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.107-3954_107-3945d others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | |||||
chr3:121840488
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107-3955_107-3945d others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | |||||
chr3:121840488
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0002t0001g0182 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.107-3955_107-3945d others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840488 | |||||
chr3:121840494
|
AAAAAAAA others(8): Show |
A | 36 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 43 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.107-3946_107-3932d others(17): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840494 | |||||
chr3:121840495
|
AAAAAAAA others(7): Show |
A | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0089others(2): Show | 5 | HG00280.hp1 HG01261.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-3945_107-3932d others(16): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840495 | |||||
chr3:121840498
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.107-3944_107-3934d others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840498 | |||||
chr3:121840504
|
AAAAAG | A | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-3944_107-3940d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840504 | |||||
chr3:121840505
|
A | G | 1 | a0001c0002t0001g0028 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.107-3948A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840505 | ||||||
chr3:121840505
|
AAAAG | A | 12 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0039others(9): Show | 14 | HG01256.hp1 HG02145.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-3944_107-3941d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840505 | |||||
chr3:121840506
|
AAAG | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 12 | HG00423.hp1 HG01109.hp1 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.107-3944_107-3942d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840506 | |||||
chr3:121840507
|
A | G | 1 | a0001c0008t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-3946A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840507 | ||||||
chr3:121840508
|
A | G | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-3945A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840508 | ||||||
chr3:121840509
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 100 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.107-3944G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840509 | ||||||
chr3:121840515
|
A | AAAAAAAA others(12): Show |
2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.107-3932_107-3931i others(21): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | |||||
chr3:121840515
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0196 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.107-3932_107-3931i others(15): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | |||||
chr3:121840515
|
A | AAAAAAAA others(5): Show |
9 | a0001c0001t0001g0031a0001c0001t0001g0191a0001c0001t0001g0198others(6): Show | 11 | HG01175.hp1 HG01515.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(14): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | |||||
chr3:121840515
|
A | AAAAAAAA others(4): Show |
17 | a0001c0001t0001g0032a0001c0001t0001g0201a0001c0001t0001g0202others(14): Show | 18 | HG00597.hp2 HG00673.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(13): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | |||||
chr3:121840515
|
A | AAAAAAAA others(3): Show |
22 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(19): Show | 40 | HG00609.hp2 HG00642.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | |||||
chr3:121840515
|
A | AAAAAAAA others(2): Show |
12 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0230others(9): Show | 14 | HG00323.hp1 HG01433.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-3932_107-3931i others(11): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | |||||
chr3:121840515
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.107-3932_107-3931i others(17): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840515 | |||||
chr3:121840515
|
A | C | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0247 | 3 | HG02040.hp1 HG03471.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.107-3938A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840515 | ||||||
chr3:121840664
|
G | A | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-3789G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840664 | ||||||
chr3:121840666
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0240 | 2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.107-3787G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840666 | ||||||
chr3:121840772
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107-3681C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840772 | ||||||
chr3:121840805
|
C | CA | 92 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(89): Show | 126 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.107-3628dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | |||||
chr3:121840805
|
C | CAA | 14 | a0001c0001t0001g0040a0001c0001t0001g0079a0001c0001t0001g0083others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.107-3629_107-3628d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | |||||
chr3:121840805
|
C | CAAA | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 83 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.107-3630_107-3628d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | |||||
chr3:121840805
|
C | CAAAA | 40 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 47 | HG00423.hp1 HG01109.hp1 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-3631_107-3628d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121840805 | |||||
chr3:121840922
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0103 | 3 | HG01169.hp2 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.107-3531C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121840922 | ||||||
chr3:121841048
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.107-3405C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841048 | ||||||
chr3:121841275
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107-3178G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841275 | ||||||
chr3:121841376
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.107-3077A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841376 | ||||||
chr3:121841496
|
C | A | 1 | a0001c0002t0001g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.107-2957C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841496 | ||||||
chr3:121841504
|
C | CAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 9 | HG00140.hp2 HG00323.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-2911_107-2910d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0001g0024a0001c0001t0001g0114a0001c0001t0001g0156others(2): Show | 6 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-2917_107-2910d others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107-2919_107-2910d others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0155a0001c0002t0001g0133a0001c0002t0001g0249 | 3 | HG01261.hp2 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.107-2921_107-2910d others(14): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.107-2923_107-2910d others(16): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAA | C | 6 | a0001c0002t0001g0110a0001c0002t0001g0112a0001c0002t0001g0116others(3): Show | 6 | HG00738.hp1 HG01081.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-2913_107-2910d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.107-2922_107-2910d others(15): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0008t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-2923_107-2910d others(16): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.107-2924_107-2910d others(17): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0002t0001g0142a0001c0002t0001g0186 | 2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.107-2925_107-2910d others(18): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(10): Show |
C | 6 | a0001c0002t0001g0025a0001c0002t0001g0072a0001c0002t0001g0073others(3): Show | 7 | HG01952.hp1 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-2926_107-2910d others(19): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(11): Show |
C | 25 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0010others(22): Show | 44 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.107-2927_107-2910d others(20): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(12): Show |
C | 3 | a0001c0002t0001g0077a0001c0002t0001g0153a0001c0002t0001g0154 | 3 | NA18946.hp1 NA18959.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.107-2928_107-2910d others(21): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841504
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.107-2929_107-2910d others(22): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841504 | |||||
chr3:121841517
|
AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01070.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.107-2932_107-2906d others(29): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841517 | |||||
chr3:121841518
|
AAAAAAAA others(19): Show |
A | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 93 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.107-2931_107-2906d others(28): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841518 | |||||
chr3:121841519
|
AAAAAAAA others(18): Show |
A | 36 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 41 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.107-2930_107-2906d others(27): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841519 | |||||
chr3:121841520
|
AAAAAAAA others(17): Show |
A | 8 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0091others(5): Show | 10 | HG01255.hp1 HG01261.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.107-2929_107-2906d others(26): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841520 | |||||
chr3:121841524
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107-2925_107-2906d others(22): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841524 | |||||
chr3:121841525
|
AAAAAAAA others(12): Show |
A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-2924_107-2906d others(21): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841525 | |||||
chr3:121841531
|
AAAAAAAA others(6): Show |
A | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(20): Show | 26 | HG00423.hp1 HG01256.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.107-2918_107-2906d others(15): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841531 | |||||
chr3:121841532
|
AAAAAAAA others(5): Show |
A | 7 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0047others(4): Show | 9 | HG01109.hp1 HG02280.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-2917_107-2906d others(14): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121841532 | |||||
chr3:121841567
|
G | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(6): Show | 11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-2886G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841567 | ||||||
chr3:121841621
|
C | A | 1 | a0001c0002t0001g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.107-2832C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841621 | ||||||
chr3:121841643
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.107-2810C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841643 | ||||||
chr3:121841794
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.107-2659G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841794 | ||||||
chr3:121841863
|
G | A | 1 | a0001c0007t0001g0200 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-2590G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841863 | ||||||
chr3:121841874
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.107-2579T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841874 | ||||||
chr3:121841875
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.107-2578G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841875 | ||||||
chr3:121841881
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.107-2572C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121841881 | ||||||
chr3:121842016
|
A | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(15): Show | 23 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.107-2437A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842016 | ||||||
chr3:121842024
|
A | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-2429A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842024 | ||||||
chr3:121842032
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.107-2421A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842032 | ||||||
chr3:121842051
|
T | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.107-2402T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842051 | ||||||
chr3:121842147
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.107-2306G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842147 | ||||||
chr3:121842148
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-2305C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842148 | ||||||
chr3:121842200
|
T | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.107-2253T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842200 | ||||||
chr3:121842250
|
G | A | 1 | a0001c0008t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-2203G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842250 | ||||||
chr3:121842256
|
C | T | 2 | a0001c0002t0001g0124a0001c0002t0001g0125 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.107-2197C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842256 | ||||||
chr3:121842287
|
T | C | 1 | a0001c0008t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-2166T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842287 | ||||||
chr3:121842552
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.107-1901G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842552 | ||||||
chr3:121842653
|
T | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 275 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.107-1800T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842653 | ||||||
chr3:121842772
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.107-1681G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842772 | ||||||
chr3:121842786
|
C | G | 1 | a0001c0001t0001g0006 | 3 | HG02280.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.107-1667C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842786 | ||||||
chr3:121842798
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.107-1655A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842798 | ||||||
chr3:121842888
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.107-1565C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842888 | ||||||
chr3:121842918
|
C | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-1535C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121842918 | ||||||
chr3:121843026
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107-1427C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843026 | ||||||
chr3:121843026
|
C | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-1427C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843026 | ||||||
chr3:121843068
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.107-1385T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843068 | ||||||
chr3:121843103
|
C | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.107-1350C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843103 | ||||||
chr3:121843243
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.107-1210C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843243 | ||||||
chr3:121843453
|
G | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-1000G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843453 | ||||||
chr3:121843457
|
C | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-996C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843457 | ||||||
chr3:121843587
|
A | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-866A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843587 | ||||||
chr3:121843633
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107-820G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121843633 | ||||||
chr3:121844073
|
T | A | 2 | a0001c0002t0001g0133a0001c0002t0001g0249 | 2 | HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.107-380T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844073 | ||||||
chr3:121844080
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.107-373G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844080 | ||||||
chr3:121844106
|
T | G | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-347T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844106 | ||||||
chr3:121844193
|
T | TG | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-259dupG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 121844193 | |||||
chr3:121844326
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.107-127G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844326 | ||||||
chr3:121844365
|
A | C | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.107-88A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844365 | ||||||
chr3:121844424
|
C | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-29C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844424 | ||||||
chr3:121844438
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.107-15T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 1/5 | chr3 | 121844438 | ||||||
chr3:121844647
|
G | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+100G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121844647 | ||||||
chr3:121844705
|
A | AT | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+158_201+159ins others(1): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121844705 | ||||||
chr3:121844881
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.201+334C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121844881 | ||||||
chr3:121845043
|
G | C | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.201+496G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845043 | ||||||
chr3:121845061
|
CA | C | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+517delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845061 | |||||
chr3:121845158
|
G | A | 9 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0112others(6): Show | 13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.201+611G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845158 | ||||||
chr3:121845221
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.201+674C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845221 | ||||||
chr3:121845268
|
A | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+721A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845268 | ||||||
chr3:121845440
|
C | CA | 53 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0002t0001g0001others(50): Show | 79 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.201+915dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845440 | |||||
chr3:121845459
|
A | AAAAAAAG | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01256.hp2 HG02738.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+915_201+916ins others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | |||||
chr3:121845459
|
A | AAAAAAG | 33 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 40 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.201+915_201+916ins others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | |||||
chr3:121845459
|
A | AAAAAAGA others(3): Show |
2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.201+915_201+916ins others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | |||||
chr3:121845459
|
A | AAAAAG | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 130 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.201+915_201+916ins others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845459 | |||||
chr3:121845459
|
A | AGAAAG | 3 | a0001c0001t0001g0192a0001c0001t0001g0240a0001c0001t0001g0242 | 3 | HG02055.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.201+912_201+913ins others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845459 | ||||||
chr3:121845459
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.201+912A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845459 | ||||||
chr3:121845789
|
AG | A | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+1246delG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121845789 | |||||
chr3:121845997
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.201+1450C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121845997 | ||||||
chr3:121846039
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.201+1492G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121846039 | ||||||
chr3:121846142
|
G | A | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+1595G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121846142 | ||||||
chr3:121846717
|
G | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+2170G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121846717 | ||||||
chr3:121846719
|
A | AT | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.201+2183dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121846719 | |||||
chr3:121847214
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.201+2667C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847214 | ||||||
chr3:121847349
|
T | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+2802T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847349 | ||||||
chr3:121847435
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.201+2888T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847435 | ||||||
chr3:121847522
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0001g0123 | 4 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+2975C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847522 | ||||||
chr3:121847613
|
A | G | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+3066A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847613 | ||||||
chr3:121847634
|
G | A | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+3087G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847634 | ||||||
chr3:121847646
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+3099G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847646 | ||||||
chr3:121847648
|
G | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0095a0001c0001t0001g0101 | 3 | HG01496.hp2 HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.201+3101G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847648 | ||||||
chr3:121847651
|
G | T | 31 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(28): Show | 35 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.201+3104G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847651 | ||||||
chr3:121847882
|
C | A | 32 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.201+3335C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847882 | ||||||
chr3:121847997
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0203a0001c0001t0001g0215others(4): Show | 8 | HG01255.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+3450C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121847997 | ||||||
chr3:121848012
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.201+3465G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848012 | ||||||
chr3:121848229
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+3682G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848229 | ||||||
chr3:121848352
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.201+3805C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848352 | ||||||
chr3:121848380
|
T | A | 1 | a0001c0001t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.201+3833T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848380 | ||||||
chr3:121848383
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.201+3836T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848383 | ||||||
chr3:121848439
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+3892T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848439 | ||||||
chr3:121848584
|
C | CT | 77 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 89 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.201+4046dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121848584 | |||||
chr3:121848613
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.201+4066G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848613 | ||||||
chr3:121848837
|
G | A | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+4290G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848837 | ||||||
chr3:121848850
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4303C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848850 | ||||||
chr3:121848851
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4304T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848851 | ||||||
chr3:121848852
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4305T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848852 | ||||||
chr3:121848853
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4306T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848853 | ||||||
chr3:121848856
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4309A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848856 | ||||||
chr3:121848858
|
A | T | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4311A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848858 | ||||||
chr3:121848859
|
A | C | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4312A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848859 | ||||||
chr3:121848860
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4313A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848860 | ||||||
chr3:121848861
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4314T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848861 | ||||||
chr3:121848862
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4315A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848862 | ||||||
chr3:121848863
|
A | T | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4316A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848863 | ||||||
chr3:121848865
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4318G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848865 | ||||||
chr3:121848866
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+4319G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848866 | ||||||
chr3:121848878
|
GC | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+4340delC | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121848878 | |||||
chr3:121848886
|
C | A | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+4339C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848886 | ||||||
chr3:121848931
|
G | A | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(35): Show | 43 | HG00423.hp1 HG01074.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+4384G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848931 | ||||||
chr3:121848942
|
A | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG02622.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.201+4395A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121848942 | ||||||
chr3:121849016
|
T | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 91 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.201+4469T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849016 | ||||||
chr3:121849190
|
G | C | 58 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0007others(55): Show | 84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.201+4643G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849190 | ||||||
chr3:121849308
|
G | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG02622.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.201+4761G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849308 | ||||||
chr3:121849330
|
T | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0095 | 2 | HG01496.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.201+4783T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849330 | ||||||
chr3:121849364
|
A | C | 1 | a0001c0001t0001g0027 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.201+4817A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849364 | ||||||
chr3:121849481
|
A | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.201+4934A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849481 | ||||||
chr3:121849667
|
G | A | 58 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0007others(55): Show | 84 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.202-5020G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849667 | ||||||
chr3:121849748
|
C | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 35 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.202-4939C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849748 | ||||||
chr3:121849849
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.202-4838A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849849 | ||||||
chr3:121849864
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.202-4823A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849864 | ||||||
chr3:121849921
|
GAT | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0236 | 5 | HG01433.hp2 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-4753_202-4752d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121849921 | |||||
chr3:121849937
|
T | C | 1 | a0001c0002t0001g0028 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.202-4750T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121849937 | ||||||
chr3:121849957
|
A | AACCTTTT others(312): Show |
19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(16): Show | 23 | HG00423.hp1 HG01109.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.202-4715_202-4714i others(321): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121849957 | |||||
chr3:121849957
|
A | AACCTTTT others(313): Show |
11 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-4715_202-4714i others(322): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121849957 | |||||
chr3:121850232
|
T | TTTTA | 245 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(242): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.202-4453_202-4450d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121850232 | |||||
chr3:121850358
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.202-4329A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850358 | ||||||
chr3:121850607
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.202-4080A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850607 | ||||||
chr3:121850619
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.202-4068A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850619 | ||||||
chr3:121850641
|
C | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0001t0001g0156others(4): Show | 8 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-4046C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850641 | ||||||
chr3:121850704
|
T | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-3983T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850704 | ||||||
chr3:121850714
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.202-3973T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850714 | ||||||
chr3:121850773
|
T | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-3914T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850773 | ||||||
chr3:121850891
|
G | C | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.202-3796G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121850891 | ||||||
chr3:121851052
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.202-3635T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851052 | ||||||
chr3:121851304
|
A | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.202-3383A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851304 | ||||||
chr3:121851351
|
G | GT | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(50): Show | 65 | HG00558.hp2 HG00642.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.202-3326dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121851351 | |||||
chr3:121851351
|
G | GTT | 13 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0037others(10): Show | 23 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-3327_202-3326d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121851351 | |||||
chr3:121851360
|
T | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0002t0001g0133others(1): Show | 4 | HG02647.hp1 HG02970.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-3327T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851360 | ||||||
chr3:121851457
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.202-3230A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851457 | ||||||
chr3:121851715
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202-2972A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851715 | ||||||
chr3:121851738
|
TG | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-2945delG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121851738 | |||||
chr3:121851848
|
T | C | 9 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0112others(6): Show | 13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.202-2839T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121851848 | ||||||
chr3:121852049
|
A | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0245 | 2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.202-2638A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852049 | ||||||
chr3:121852714
|
A | G | 2 | a0001c0002t0001g0128a0001c0002t0001g0131 | 2 | NA18967.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.202-1973A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852714 | ||||||
chr3:121852975
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202-1712T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852975 | ||||||
chr3:121852984
|
A | G | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.202-1703A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121852984 | ||||||
chr3:121853061
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202-1626T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853061 | ||||||
chr3:121853169
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-1518T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853169 | ||||||
chr3:121853247
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-1440C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853247 | ||||||
chr3:121853286
|
G | T | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.202-1401G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853286 | ||||||
chr3:121853405
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.202-1282T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853405 | ||||||
chr3:121853413
|
C | T | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.202-1274C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853413 | ||||||
chr3:121853475
|
G | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-1212G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853475 | ||||||
chr3:121853525
|
C | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-1162C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853525 | ||||||
chr3:121853852
|
T | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.202-835T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121853852 | ||||||
chr3:121854015
|
A | G | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.202-672A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854015 | ||||||
chr3:121854176
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-511C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854176 | ||||||
chr3:121854180
|
G | A | 3 | a0002c0003t0001g0190a0002c0003t0001g0197a0002c0003t0001g0206 | 3 | HG02027.hp2 HG02074.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.202-507G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854180 | ||||||
chr3:121854315
|
C | CA | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 141 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.202-353dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121854315 | |||||
chr3:121854315
|
C | CAA | 82 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 113 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.202-354_202-353dup others(2): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 121854315 | |||||
chr3:121854576
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.202-111G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854576 | ||||||
chr3:121854588
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.202-99A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854588 | ||||||
chr3:121854608
|
C | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-79C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 2/5 | chr3 | 121854608 | ||||||
chr3:121854882
|
T | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.338+59T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121854882 | ||||||
chr3:121855003
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 266 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.338+180T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855003 | ||||||
chr3:121855084
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.338+261C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855084 | ||||||
chr3:121855321
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(6): Show | 11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.338+498T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855321 | ||||||
chr3:121855325
|
C | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.338+502C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855325 | ||||||
chr3:121855368
|
T | C | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.338+545T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855368 | ||||||
chr3:121855372
|
C | T | 41 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(38): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.338+549C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855372 | ||||||
chr3:121855384
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0085 | 2 | HG01361.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.338+561T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855384 | ||||||
chr3:121855386
|
G | A | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.338+563G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855386 | ||||||
chr3:121855411
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.338+588G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855411 | ||||||
chr3:121855622
|
C | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+799C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121855622 | ||||||
chr3:121856242
|
G | A | 1 | a0001c0002t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.339-769G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856242 | ||||||
chr3:121856319
|
C | CT | 17 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0041others(14): Show | 19 | HG00280.hp1 HG01074.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.339-678dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 121856319 | |||||
chr3:121856319
|
C | CTTT | 32 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(29): Show | 37 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.339-680_339-678dup others(3): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 121856319 | |||||
chr3:121856365
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.339-646T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856365 | ||||||
chr3:121856395
|
T | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-616T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856395 | ||||||
chr3:121856696
|
G | A | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.339-315G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856696 | ||||||
chr3:121856929
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.339-82G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 3/5 | chr3 | 121856929 | ||||||
chr3:121857181
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.484+25C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857181 | ||||||
chr3:121857268
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.484+112C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857268 | ||||||
chr3:121857574
|
G | A | 2 | a0001c0002t0001g0124a0001c0002t0001g0125 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.484+418G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857574 | ||||||
chr3:121857591
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.484+435A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857591 | ||||||
chr3:121857649
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.484+493A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857649 | ||||||
chr3:121857655
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.484+499A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857655 | ||||||
chr3:121857673
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+517T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857673 | ||||||
chr3:121857705
|
G | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.484+549G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857705 | ||||||
chr3:121857856
|
T | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0096others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+700T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857856 | ||||||
chr3:121857894
|
C | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0240a0001c0001t0001g0242 | 3 | HG02055.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.484+738C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121857894 | ||||||
chr3:121858018
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.484+862C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858018 | ||||||
chr3:121858131
|
C | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 57 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.484+975C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858131 | ||||||
chr3:121858255
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.484+1099G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858255 | ||||||
chr3:121858786
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+1630C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858786 | ||||||
chr3:121858917
|
T | G | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.484+1761T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858917 | ||||||
chr3:121858921
|
C | T | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+1765C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121858921 | ||||||
chr3:121859054
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.484+1898G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859054 | ||||||
chr3:121859113
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 36 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.484+1957G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859113 | ||||||
chr3:121859121
|
T | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.484+1965T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859121 | ||||||
chr3:121859220
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.484+2064G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859220 | ||||||
chr3:121859362
|
T | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+2206T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859362 | ||||||
chr3:121859474
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+2318T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859474 | ||||||
chr3:121859569
|
G | T | 1 | a0001c0002t0001g0148 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.484+2413G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859569 | ||||||
chr3:121859693
|
G | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+2537G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859693 | ||||||
chr3:121859840
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.484+2684C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859840 | ||||||
chr3:121859900
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.484+2744G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859900 | ||||||
chr3:121859930
|
T | C | 52 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(49): Show | 59 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.484+2774T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859930 | ||||||
chr3:121859991
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01433.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+2835T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121859991 | ||||||
chr3:121860000
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0191a0001c0001t0001g0209others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.484+2844C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860000 | ||||||
chr3:121860104
|
G | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+2948G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860104 | ||||||
chr3:121860219
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG01884.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.484+3063C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860219 | ||||||
chr3:121860301
|
G | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(6): Show | 11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.484+3145G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860301 | ||||||
chr3:121860367
|
G | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0145 | 2 | NA18941.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.484+3211G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860367 | ||||||
chr3:121860389
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+3233T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860389 | ||||||
chr3:121860435
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+3279C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860435 | ||||||
chr3:121860679
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484+3523C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860679 | ||||||
chr3:121860752
|
C | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+3596C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860752 | ||||||
chr3:121860824
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.484+3668C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860824 | ||||||
chr3:121860916
|
A | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.484+3760A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860916 | ||||||
chr3:121860947
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.484+3791G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121860947 | ||||||
chr3:121861018
|
C | T | 1 | a0001c0002t0001g0147 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.484+3862C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861018 | ||||||
chr3:121861119
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.484+3963T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861119 | ||||||
chr3:121861131
|
A | G | 1 | a0001c0001t0001g0006 | 3 | HG02280.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.484+3975A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861131 | ||||||
chr3:121861269
|
G | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+4113G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861269 | ||||||
chr3:121861365
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(6): Show | 11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.484+4209G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861365 | ||||||
chr3:121861486
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+4330T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861486 | ||||||
chr3:121861596
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+4440T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121861596 | ||||||
chr3:121862277
|
T | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+5121T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862277 | ||||||
chr3:121862344
|
G | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.484+5188G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862344 | ||||||
chr3:121862409
|
T | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.484+5253T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862409 | ||||||
chr3:121862436
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+5280A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862436 | ||||||
chr3:121862498
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.484+5342C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862498 | ||||||
chr3:121862576
|
C | CT | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+5426dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121862576 | |||||
chr3:121862688
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.484+5532C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121862688 | ||||||
chr3:121863171
|
C | T | 1 | a0001c0001t0001g0019 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.484+6015C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863171 | ||||||
chr3:121863293
|
G | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(35): Show | 43 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.484+6137G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863293 | ||||||
chr3:121863405
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.484+6249G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863405 | ||||||
chr3:121863459
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.484+6303A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863459 | ||||||
chr3:121863477
|
G | A | 1 | a0001c0008t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.484+6321G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863477 | ||||||
chr3:121863501
|
G | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0130 | 7 | HG02015.hp2 HG02027.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.484+6345G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863501 | ||||||
chr3:121863505
|
C | T | 7 | a0001c0001t0001g0115a0001c0001t0001g0139a0001c0001t0001g0175others(4): Show | 9 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.484+6349C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863505 | ||||||
chr3:121863789
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+6633G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121863789 | ||||||
chr3:121864367
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.484+7211C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864367 | ||||||
chr3:121864545
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+7389G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864545 | ||||||
chr3:121864568
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 266 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.484+7412T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864568 | ||||||
chr3:121864637
|
A | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01433.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+7481A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864637 | ||||||
chr3:121864652
|
CAA | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 119 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.484+7502_484+7503d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121864652 | |||||
chr3:121864659
|
A | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 119 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.484+7503A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864659 | ||||||
chr3:121864711
|
G | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.484+7555G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864711 | ||||||
chr3:121864738
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.484+7582C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864738 | ||||||
chr3:121864744
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.484+7588G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864744 | ||||||
chr3:121864848
|
G | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-7689G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121864848 | ||||||
chr3:121865218
|
G | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-7319G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865218 | ||||||
chr3:121865291
|
G | GGTTAA | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-7245_485-7241d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121865291 | |||||
chr3:121865622
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.485-6915G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865622 | ||||||
chr3:121865672
|
AT | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-6864delT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865672 | ||||||
chr3:121865673
|
TA | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01433.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-6863delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865673 | ||||||
chr3:121865675
|
T | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044 | 3 | HG01074.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.485-6862T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865675 | ||||||
chr3:121865731
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.485-6806A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865731 | ||||||
chr3:121865959
|
A | T | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485-6578A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865959 | ||||||
chr3:121865998
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485-6539G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121865998 | ||||||
chr3:121866152
|
C | T | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 52 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.485-6385C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866152 | ||||||
chr3:121866299
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 266 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.485-6238T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866299 | ||||||
chr3:121866304
|
C | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-6233C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866304 | ||||||
chr3:121866609
|
C | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-5928C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866609 | ||||||
chr3:121866732
|
T | TA | 9 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0112others(6): Show | 13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.485-5797dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121866732 | |||||
chr3:121866748
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.485-5789T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866748 | ||||||
chr3:121866754
|
G | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-5783G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866754 | ||||||
chr3:121866784
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.485-5753G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121866784 | ||||||
chr3:121867539
|
T | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-4998T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867539 | ||||||
chr3:121867639
|
G | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 266 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.485-4898G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867639 | ||||||
chr3:121867820
|
C | T | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-4717C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867820 | ||||||
chr3:121867830
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.485-4707A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867830 | ||||||
chr3:121867934
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0067 | 5 | NA18992.hp2 NA19005.hp2 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-4603G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121867934 | ||||||
chr3:121868017
|
A | T | 9 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0112others(6): Show | 13 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.485-4520A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868017 | ||||||
chr3:121868233
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.485-4304T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868233 | ||||||
chr3:121868235
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.485-4302T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868235 | ||||||
chr3:121868279
|
A | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-4258A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868279 | ||||||
chr3:121868320
|
C | T | 1 | a0001c0002t0001g0150 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.485-4217C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868320 | ||||||
chr3:121868365
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(6): Show | 11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-4172G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868365 | ||||||
chr3:121868425
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-4112C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868425 | ||||||
chr3:121868437
|
A | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0059a0001c0001t0001g0062others(6): Show | 9 | HG00673.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-4100A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868437 | ||||||
chr3:121868463
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.485-4074G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868463 | ||||||
chr3:121868537
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.485-4000G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868537 | ||||||
chr3:121868555
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485-3982G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868555 | ||||||
chr3:121868603
|
T | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-3934T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868603 | ||||||
chr3:121868686
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.485-3851C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868686 | ||||||
chr3:121868750
|
A | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485-3787A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868750 | ||||||
chr3:121868768
|
A | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG01884.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485-3769A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868768 | ||||||
chr3:121868787
|
C | G | 1 | a0001c0002t0001g0028 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.485-3750C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868787 | ||||||
chr3:121868890
|
A | T | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-3647A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121868890 | ||||||
chr3:121869027
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.485-3510A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869027 | ||||||
chr3:121869157
|
C | T | 1 | a0001c0002t0001g0144 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.485-3380C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869157 | ||||||
chr3:121869416
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-3121A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869416 | ||||||
chr3:121869463
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 40 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.485-3074A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869463 | ||||||
chr3:121869494
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.485-3043C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869494 | ||||||
chr3:121869654
|
G | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2883G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869654 | ||||||
chr3:121869717
|
T | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2820T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869717 | ||||||
chr3:121869718
|
T | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-2819T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869718 | ||||||
chr3:121869937
|
G | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.485-2600G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869937 | ||||||
chr3:121869996
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.485-2541G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121869996 | ||||||
chr3:121870061
|
A | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2476A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870061 | ||||||
chr3:121870065
|
C | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-2472C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870065 | ||||||
chr3:121870097
|
A | ATTT | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-2439_485-2437d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121870097 | |||||
chr3:121870538
|
A | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 44 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.485-1999A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870538 | ||||||
chr3:121870566
|
A | C | 1 | a0001c0002t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.485-1971A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870566 | ||||||
chr3:121870705
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01074.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.485-1832A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870705 | ||||||
chr3:121870750
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-1787T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870750 | ||||||
chr3:121870756
|
G | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(6): Show | 11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-1781G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870756 | ||||||
chr3:121870813
|
T | C | 1 | a0001c0002t0001g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.485-1724T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870813 | ||||||
chr3:121870828
|
G | T | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-1709G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870828 | ||||||
chr3:121870867
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.485-1670C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121870867 | ||||||
chr3:121871169
|
T | TATATA | 2 | a0001c0001t0001g0018a0001c0001t0001g0168 | 3 | HG01069.hp2 HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-1348_485-1344d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121871169 | |||||
chr3:121871180
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.485-1357A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871180 | ||||||
chr3:121871285
|
C | T | 3 | a0001c0001t0001g0205a0001c0002t0001g0118a0001c0002t0001g0144 | 3 | HG00673.hp2 HG03927.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.485-1252C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871285 | ||||||
chr3:121871317
|
AGAATAGA others(1): Show |
A | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 56 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.485-1211_485-1204d others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121871317 | |||||
chr3:121871326
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.485-1211G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871326 | ||||||
chr3:121871523
|
G | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-1014G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871523 | ||||||
chr3:121871564
|
A | G | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-973A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871564 | ||||||
chr3:121871706
|
A | G | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-831A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121871706 | ||||||
chr3:121872087
|
GA | G | 36 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(33): Show | 41 | HG00423.hp1 HG00673.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.485-447delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 121872087 | |||||
chr3:121872112
|
T | C | 1 | a0001c0002t0001g0143 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.485-425T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121872112 | ||||||
chr3:121872158
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.485-379T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121872158 | ||||||
chr3:121872223
|
A | G | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.485-314A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 4/5 | chr3 | 121872223 | ||||||
chr3:121873052
|
G | C | 1 | a0001c0001t0001g0231 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.736+264G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873052 | ||||||
chr3:121873115
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0098 | 4 | HG02280.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+327C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873115 | ||||||
chr3:121873560
|
A | T | 32 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(29): Show | 37 | HG00423.hp1 HG00673.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.736+772A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873560 | ||||||
chr3:121873574
|
T | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0202others(8): Show | 13 | HG00673.hp1 HG01975.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.736+786T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873574 | ||||||
chr3:121873575
|
T | A | 1 | a0001c0001t0001g0139 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.736+787T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873575 | ||||||
chr3:121873807
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.736+1019T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121873807 | ||||||
chr3:121873817
|
TTTAGA | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.736+1033_736+1037d others(7): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121873817 | |||||
chr3:121874421
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.736+1633G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121874421 | ||||||
chr3:121874468
|
T | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.736+1680T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121874468 | ||||||
chr3:121874922
|
G | A | 48 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(45): Show | 54 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.736+2134G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121874922 | ||||||
chr3:121875196
|
G | T | 1 | a0001c0002t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.736+2408G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875196 | ||||||
chr3:121875414
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.736+2626T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875414 | ||||||
chr3:121875421
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0172 | 2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.736+2633G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875421 | ||||||
chr3:121875676
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.736+2888C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875676 | ||||||
chr3:121875755
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.736+2967A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875755 | ||||||
chr3:121875844
|
AG | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.736+3057delG | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121875844 | ||||||
chr3:121876646
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG00140.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.736+3858G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121876646 | ||||||
chr3:121876881
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.736+4093G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121876881 | ||||||
chr3:121876889
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+4101G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121876889 | ||||||
chr3:121877008
|
GAGAT | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+4224_736+4227d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121877008 | |||||
chr3:121877010
|
GAT | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+4224_736+4225d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121877010 | |||||
chr3:121877029
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.736+4241G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877029 | ||||||
chr3:121877089
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.736+4301G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877089 | ||||||
chr3:121877648
|
G | GAAC | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.736+4862_736+4864d others(5): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121877648 | |||||
chr3:121877875
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.736+5087G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877875 | ||||||
chr3:121877897
|
T | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+5109T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877897 | ||||||
chr3:121877960
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.736+5172T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121877960 | ||||||
chr3:121878175
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.736+5387G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878175 | ||||||
chr3:121878191
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.736+5403G>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878191 | ||||||
chr3:121878447
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.736+5659A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878447 | ||||||
chr3:121878475
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736+5687T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878475 | ||||||
chr3:121878596
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.736+5808C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878596 | ||||||
chr3:121878699
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+5911C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878699 | ||||||
chr3:121878802
|
T | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.736+6014T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878802 | ||||||
chr3:121878833
|
A | G | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.736+6045A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878833 | ||||||
chr3:121878935
|
T | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0069others(6): Show | 11 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.736+6147T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878935 | ||||||
chr3:121878948
|
T | C | 1 | a0001c0002t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.736+6160T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121878948 | ||||||
chr3:121879030
|
T | A | 1 | a0001c0002t0001g0146 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.736+6242T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879030 | ||||||
chr3:121879041
|
T | C | 48 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(45): Show | 54 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.736+6253T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879041 | ||||||
chr3:121879051
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.736+6263A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879051 | ||||||
chr3:121879153
|
T | C | 48 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(45): Show | 54 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.736+6365T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879153 | ||||||
chr3:121879155
|
TA | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0199 | 4 | HG02015.hp1 NA18941.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+6371delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121879155 | |||||
chr3:121879292
|
G | T | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.736+6504G>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879292 | ||||||
chr3:121879450
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 87 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.736+6662A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879450 | ||||||
chr3:121879467
|
T | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.736+6679T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121879467 | ||||||
chr3:121879620
|
C | CTT | 192 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.737-6712_737-6711d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121879620 | |||||
chr3:121880308
|
AT | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.737-6020delT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880308 | |||||
chr3:121880455
|
G | GGTGTGT | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0070others(6): Show | 11 | HG00735.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-5854_737-5849d others(8): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | |||||
chr3:121880455
|
G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0069a0001c0001t0001g0108a0001c0001t0001g0166others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.737-5856_737-5849d others(10): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | |||||
chr3:121880455
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0027 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.737-5858_737-5849d others(12): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | |||||
chr3:121880455
|
GGT | G | 83 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(80): Show | 115 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.737-5850_737-5849d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | |||||
chr3:121880455
|
GGTGT | G | 47 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(44): Show | 53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.737-5852_737-5849d others(6): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | |||||
chr3:121880455
|
GGTGTGT | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 78 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.737-5854_737-5849d others(8): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121880455 | |||||
chr3:121880461
|
T | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0177 | 2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.737-5881T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880461 | ||||||
chr3:121880463
|
T | G | 1 | a0001c0001t0001g0005 | 4 | HG02257.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.737-5879T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880463 | ||||||
chr3:121880465
|
T | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0058 | 2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.737-5877T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880465 | ||||||
chr3:121880501
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.737-5841A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880501 | ||||||
chr3:121880784
|
C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.737-5558C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880784 | ||||||
chr3:121880785
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.737-5557G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880785 | ||||||
chr3:121880825
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.737-5517G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121880825 | ||||||
chr3:121881074
|
T | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(2): Show | 5 | HG01074.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.737-5268T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881074 | ||||||
chr3:121881129
|
C | T | 40 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0026others(37): Show | 45 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.737-5213C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881129 | ||||||
chr3:121881264
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.737-5078C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881264 | ||||||
chr3:121881465
|
A | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 7 | HG00735.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-4877A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881465 | ||||||
chr3:121881845
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.737-4497A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881845 | ||||||
chr3:121881984
|
T | C | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(13): Show | 19 | HG00735.hp2 HG02258.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-4358T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121881984 | ||||||
chr3:121882147
|
A | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.737-4195A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882147 | ||||||
chr3:121882314
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.737-4028A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882314 | ||||||
chr3:121882348
|
CAA | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.737-3980_737-3979d others(4): Show |
EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121882348 | |||||
chr3:121882529
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.737-3813T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882529 | ||||||
chr3:121882663
|
A | G | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 118 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.737-3679A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882663 | ||||||
chr3:121882685
|
C | A | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.737-3657C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882685 | ||||||
chr3:121882730
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(13): Show | 19 | HG00735.hp2 HG02258.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-3612C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882730 | ||||||
chr3:121882787
|
G | GT | 131 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0020others(128): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.737-3543dupT | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121882787 | |||||
chr3:121882947
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.737-3395C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121882947 | ||||||
chr3:121883207
|
C | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.737-3135C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883207 | ||||||
chr3:121883284
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.737-3058A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883284 | ||||||
chr3:121883495
|
T | C | 1 | a0003c0005t0001g0029 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.737-2847T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883495 | ||||||
chr3:121883572
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.737-2770G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883572 | ||||||
chr3:121883733
|
A | G | 4 | a0001c0001t0001g0198a0001c0001t0001g0211a0001c0001t0001g0221others(1): Show | 5 | HG02723.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-2609A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883733 | ||||||
chr3:121883775
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.737-2567C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883775 | ||||||
chr3:121883813
|
C | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.737-2529C>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121883813 | ||||||
chr3:121884156
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.737-2186G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884156 | ||||||
chr3:121884179
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-2163A>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884179 | ||||||
chr3:121884217
|
G | A | 2 | a0001c0002t0001g0142a0001c0002t0001g0186 | 2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.737-2125G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884217 | ||||||
chr3:121884288
|
T | C | 16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(13): Show | 19 | HG00735.hp2 HG02258.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-2054T>C | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884288 | ||||||
chr3:121884312
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 36 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.737-2030C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884312 | ||||||
chr3:121884340
|
C | CA | 53 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0021others(50): Show | 61 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.737-1985dupA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121884340 | |||||
chr3:121884340
|
CA | C | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(21): Show | 27 | HG00423.hp1 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.737-1985delA | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 121884340 | |||||
chr3:121884435
|
A | T | 7 | a0001c0002t0001g0008a0001c0002t0001g0112a0001c0002t0001g0116others(4): Show | 9 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-1907A>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884435 | ||||||
chr3:121884439
|
T | A | 1 | a0001c0008t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.737-1903T>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884439 | ||||||
chr3:121884616
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.737-1726G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884616 | ||||||
chr3:121884679
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.737-1663C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884679 | ||||||
chr3:121884685
|
G | A | 2 | a0001c0002t0001g0110a0001c0002t0001g0111 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.737-1657G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884685 | ||||||
chr3:121884715
|
GC | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0020others(127): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.737-1626delC | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884715 | ||||||
chr3:121884724
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.737-1618A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121884724 | ||||||
chr3:121885209
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.737-1133A>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885209 | ||||||
chr3:121885376
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.737-966C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885376 | ||||||
chr3:121885617
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.737-725C>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885617 | ||||||
chr3:121885773
|
C | T | 2 | a0001c0002t0001g0142a0001c0002t0001g0186 | 2 | NA19062.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.737-569C>T | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121885773 | ||||||
chr3:121886057
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.737-285G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121886057 | ||||||
chr3:121886089
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.737-253G>A | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121886089 | ||||||
chr3:121886093
|
T | G | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.737-249T>G | EAF2 | ENSG00000145088.9 | transcript | ENST00000273668.7 | protein_coding | 5/5 | chr3 | 121886093 |