Item | Value |
---|---|
geneid | 9695 |
ensemblid | ENSG00000134109.11 |
hgncid | 18967 |
symbol | EDEM1 |
name | ER degradation enhancing alpha-mannosidase like protein 1 |
refseq_nuc | NM_014674.3 |
refseq_prot | NP_055489.1 |
ensembl_nuc | ENST00000256497.9 |
ensembl_prot | ENSP00000256497.4 |
mane_status | MANE Select |
chr | chr3 |
start | 5187707 |
end | 5219958 |
strand | + |
ver | v1.2 |
region | chr3:5187707-5219958 |
region5000 | chr3:5182707-5224958 |
regionname0 | EDEM1_chr3_5187707_5219958 |
regionname5000 | EDEM1_chr3_5182707_5224958 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 657 | 361 | 92 | 66 | 149 | 14 | 38 | 119 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0002 | 0/0 | 657 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0003 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0004 | 0/0 | 657 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0005 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0006 | 0/0 | 657 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0007 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1974 | 315 | 75 | 64 | 133 | 14 | 28 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0002 | 1/0 | 1974 | 30 | 8 | 1 | 14 | 0 | 6 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0003 | 0/0 | 1974 | 8 | 0 | 0 | 8 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0004 | 0/0 | 1974 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0005 | 0/0 | 1974 | 3 | 1 | 1 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0006 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0007 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0008 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0009 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0010 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0011 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0012 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0013 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0014 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0015 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0016 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0017 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
c0018 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4140 | 84 | 7 | 25 | 43 | 2 | 7 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0002 | 0/0 | 4140 | 61 | 5 | 14 | 31 | 8 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0003 | 0/0 | 4140 | 39 | 0 | 6 | 30 | 0 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0004 | 0/0 | 4140 | 37 | 12 | 0 | 22 | 1 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0005 | 0/0 | 4138 | 18 | 4 | 1 | 11 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0006 | 0/0 | 4140 | 14 | 7 | 1 | 4 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0007 | 0/0 | 4140 | 11 | 6 | 0 | 3 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0008 | 0/1 | 4140 | 9 | 5 | 3 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0009 | 0/0 | 4140 | 8 | 0 | 3 | 4 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0010 | 0/0 | 4140 | 6 | 0 | 6 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0011 | 0/0 | 4141 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0012 | 0/0 | 4138 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0013 | 0/0 | 4140 | 5 | 1 | 2 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0014 | 0/0 | 4139 | 4 | 4 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0015 | 0/0 | 4139 | 4 | 1 | 0 | 1 | 1 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0016 | 0/0 | 4138 | 4 | 1 | 0 | 0 | 0 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0017 | 0/0 | 4139 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0018 | 0/0 | 4140 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0019 | 0/0 | 4140 | 3 | 2 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0020 | 0/0 | 4138 | 3 | 1 | 0 | 1 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0021 | 0/0 | 4140 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0022 | 0/0 | 4141 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0023 | 0/0 | 4141 | 2 | 0 | 1 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0024 | 0/0 | 4140 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0025 | 0/0 | 4140 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0026 | 0/0 | 4140 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0027 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0028 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0029 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0030 | 0/0 | 4138 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0031 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0032 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0033 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0034 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0035 | 0/0 | 4141 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0036 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0037 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0038 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0039 | 0/0 | 4141 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0040 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0041 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0042 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0043 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0044 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0045 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0046 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0047 | 0/0 | 4141 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0048 | 0/0 | 4138 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0049 | 0/0 | 4138 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0050 | 0/0 | 4138 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0051 | 0/0 | 4138 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0052 | 0/0 | 4138 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0053 | 0/0 | 4138 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0054 | 0/0 | 4138 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0055 | 1/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0056 | 0/0 | 4140 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0057 | 0/0 | 4140 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0058 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0059 | 0/0 | 4140 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0060 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0061 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
t0062 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 27 | 3 | 5 | 15 | 0 | 4 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0002 | 0/0 | 11 | 0 | 1 | 7 | 1 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0003 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0005 | 0/0 | 6 | 2 | 1 | 1 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0009 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0011 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1974 | 315 | 75 | 64 | 133 | 14 | 28 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0002 | 1/0 | 1974 | 30 | 8 | 1 | 14 | 0 | 6 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0004 | 0/0 | 1974 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0005 | 0/0 | 1974 | 3 | 1 | 1 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0006 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0007 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0008 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0012 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0013 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0014 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0016 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0001c0018 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0002c0003 | 0/0 | 1974 | 8 | 0 | 0 | 8 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0003c0017 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0004c0009 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0005c0011 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0006c0010 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 | |
a0007c0015 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6113 | 76 | 7 | 25 | 37 | 2 | 5 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0002 | 0/0 | 6113 | 59 | 5 | 14 | 29 | 8 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0003 | 0/0 | 6113 | 34 | 0 | 6 | 25 | 0 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0004 | 0/0 | 6113 | 36 | 11 | 0 | 22 | 1 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0005 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0006 | 0/0 | 6113 | 14 | 7 | 1 | 4 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0007 | 0/0 | 6113 | 11 | 6 | 0 | 3 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0008 | 0/1 | 6113 | 9 | 5 | 3 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0009 | 0/0 | 6113 | 6 | 0 | 2 | 3 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0010 | 0/0 | 6113 | 6 | 0 | 6 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0011 | 0/0 | 6114 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0012 | 0/0 | 6111 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0013 | 0/0 | 6113 | 5 | 1 | 2 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0015 | 0/0 | 6112 | 4 | 1 | 0 | 1 | 1 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0016 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0017 | 0/0 | 6112 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0018 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0019 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0020 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0021 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0022 | 0/0 | 6114 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0023 | 0/0 | 6114 | 2 | 0 | 1 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0024 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0025 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0027 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0030 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0032 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0033 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0035 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0036 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0038 | 0/0 | 6112 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0039 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0040 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0041 | 0/0 | 6112 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0042 | 0/0 | 6112 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0043 | 0/0 | 6112 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0044 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0045 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0046 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0047 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0048 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0050 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0052 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0056 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0057 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0059 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0060 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0061 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0001t0062 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0001 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0005 | 0/0 | 6111 | 17 | 4 | 1 | 10 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0016 | 0/0 | 6111 | 3 | 0 | 0 | 0 | 0 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0018 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0020 | 0/0 | 6111 | 2 | 1 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0026 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0051 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0053 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0054 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0002t0055 | 1/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0004t0014 | 0/0 | 6112 | 4 | 4 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0004t0029 | 0/0 | 6112 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0005t0001 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0005t0004 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0005t0009 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0006t0002 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0007t0028 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0008t0049 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0012t0058 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0013t0009 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0014t0037 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0016t0034 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0001c0018t0031 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0002c0003t0001 | 0/0 | 6113 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0002c0003t0003 | 0/0 | 6113 | 5 | 0 | 0 | 5 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0003c0017t0001 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0004c0009t0019 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0005c0011t0002 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0006c0010t0001 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
a0007c0015t0001 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | copy fasta | chr3 | 5182707 | 5224958 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 1 | 5 | 10 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0001 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0009g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0009g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0010g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0010g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0010g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0012g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0013g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0013g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0013g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0015g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0015g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0015g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0017g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0018g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0018g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0019g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0019g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0020g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0021g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0021g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0022g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0023g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0023g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0024g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0025g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0025g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0027g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0030g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0033g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0035g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0036g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0038g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0039g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0040g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0041g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0042g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0043g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0044g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0045g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0046g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0047g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0048g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0050g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0052g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0056g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0057g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0059g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0060g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0061g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0001t0062g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0016g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0016g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0016g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0018g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0020g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0020g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0026g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0051g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0053g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0054g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0002t0055g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0004t0014g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0004t0014g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0004t0029g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0005t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0005t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0006t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0007t0028g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0008t0049g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0012t0058g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0013t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0014t0037g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0016t0034g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0001c0018t0031g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0002c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0002c0003t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0002c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0003c0017t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0004c0009t0019g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0005c0011t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0006c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
a0007c0015t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0176 | EUR | GBR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00280 | hp2 | a0001 | c0001 | t0023 | g0009 | EUR | FIN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00438 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00558 | hp1 | a0001 | c0002 | t0005 | g0231 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00558 | hp2 | a0005 | c0011 | t0002 | g0026 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00639 | hp2 | a0001 | c0001 | t0056 | g0044 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00735 | hp2 | a0001 | c0001 | t0010 | g0045 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00738 | hp2 | a0001 | c0001 | t0023 | g0251 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01070 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01074 | hp2 | a0001 | c0001 | t0013 | g0006 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01106 | hp1 | a0001 | c0001 | t0048 | g0090 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01109 | hp1 | a0001 | c0002 | t0005 | g0083 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01169 | hp2 | a0001 | c0001 | t0013 | g0131 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01175 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01243 | hp1 | a0001 | c0001 | t0038 | g0060 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0051 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0011 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01256 | hp2 | a0001 | c0005 | t0009 | g0114 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01258 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01346 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01433 | hp1 | a0001 | c0001 | t0057 | g0048 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01433 | hp2 | a0001 | c0001 | t0010 | g0006 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01496 | hp2 | a0001 | c0001 | t0009 | g0254 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01515 | hp1 | a0001 | c0001 | t0015 | g0027 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01515 | hp2 | a0001 | c0001 | t0042 | g0206 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01891 | hp1 | a0001 | c0001 | t0019 | g0221 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01891 | hp2 | a0001 | c0001 | t0036 | g0155 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02027 | hp1 | a0001 | c0001 | t0025 | g0213 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02055 | hp2 | a0001 | c0001 | t0021 | g0093 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02071 | hp1 | a0002 | c0003 | t0003 | g0033 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02083 | hp2 | a0001 | c0001 | t0015 | g0166 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02129 | hp1 | a0001 | c0002 | t0005 | g0236 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02135 | hp1 | a0001 | c0002 | t0005 | g0013 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | CDX | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02258 | hp1 | a0001 | c0001 | t0027 | g0092 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02258 | hp2 | a0001 | c0001 | t0052 | g0217 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02280 | hp1 | a0001 | c0012 | t0058 | g0111 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0087 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02451 | hp2 | a0001 | c0005 | t0004 | g0113 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0204 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02572 | hp1 | a0001 | c0004 | t0029 | g0063 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0243 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02602 | hp1 | a0001 | c0002 | t0005 | g0077 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0193 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02622 | hp1 | a0001 | c0001 | t0045 | g0214 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02622 | hp2 | a0001 | c0001 | t0021 | g0094 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02630 | hp1 | a0001 | c0001 | t0061 | g0085 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0234 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02647 | hp1 | a0001 | c0002 | t0005 | g0246 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02647 | hp2 | a0001 | c0001 | t0024 | g0005 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0225 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0039 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02735 | hp2 | a0001 | c0001 | t0015 | g0252 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02738 | hp1 | a0001 | c0001 | t0022 | g0042 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02738 | hp2 | a0001 | c0005 | t0001 | g0165 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02809 | hp2 | a0001 | c0001 | t0024 | g0005 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02818 | hp2 | a0001 | c0001 | t0016 | g0056 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02886 | hp2 | a0001 | c0001 | t0017 | g0064 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0233 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02895 | hp2 | a0001 | c0002 | t0020 | g0245 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0215 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0232 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02922 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0039 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0224 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02976 | hp1 | a0001 | c0001 | t0015 | g0017 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02976 | hp2 | a0001 | c0004 | t0014 | g0012 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03017 | hp1 | a0001 | c0008 | t0049 | g0183 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03041 | hp1 | a0001 | c0001 | t0018 | g0091 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0229 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0223 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03195 | hp1 | a0001 | c0002 | t0054 | g0075 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03209 | hp1 | a0001 | c0004 | t0014 | g0012 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03225 | hp1 | a0001 | c0002 | t0005 | g0025 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0210 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03453 | hp1 | a0001 | c0001 | t0013 | g0050 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03490 | hp1 | a0006 | c0010 | t0001 | g0001 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0207 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03516 | hp1 | a0001 | c0004 | t0014 | g0012 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03540 | hp2 | a0001 | c0001 | t0011 | g0247 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03669 | hp2 | a0001 | c0002 | t0016 | g0078 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03688 | hp1 | a0001 | c0001 | t0009 | g0146 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03688 | hp2 | a0001 | c0002 | t0016 | g0013 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03704 | hp2 | a0001 | c0002 | t0016 | g0069 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03710 | hp1 | a0001 | c0001 | t0032 | g0001 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03710 | hp2 | a0001 | c0001 | t0013 | g0160 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03831 | hp1 | a0001 | c0002 | t0020 | g0081 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03831 | hp2 | a0001 | c0016 | t0034 | g0002 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03834 | hp1 | a0001 | c0001 | t0059 | g0047 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03834 | hp2 | a0001 | c0001 | t0033 | g0005 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03927 | hp1 | a0001 | c0001 | t0046 | g0226 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03942 | hp1 | a0001 | c0007 | t0028 | g0150 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04115 | hp2 | a0001 | c0001 | t0022 | g0042 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04204 | hp1 | a0001 | c0001 | t0007 | g0238 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04204 | hp2 | a0004 | c0009 | t0019 | g0001 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG04228 | hp2 | a0001 | c0002 | t0005 | g0084 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0237 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18747 | hp2 | a0003 | c0017 | t0001 | g0001 | EAS | CHB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0079 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18942 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18943 | hp1 | a0001 | c0002 | t0005 | g0024 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18943 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18945 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18950 | hp2 | a0001 | c0001 | t0025 | g0212 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18952 | hp1 | a0001 | c0002 | t0005 | g0013 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18957 | hp2 | a0001 | c0001 | t0009 | g0096 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18961 | hp2 | a0001 | c0001 | t0062 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18962 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18965 | hp1 | a0001 | c0006 | t0002 | g0163 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18966 | hp2 | a0001 | c0001 | t0043 | g0008 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18969 | hp1 | a0001 | c0002 | t0026 | g0082 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18975 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18986 | hp1 | a0001 | c0001 | t0060 | g0156 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18986 | hp2 | a0001 | c0002 | t0005 | g0074 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18989 | hp2 | a0001 | c0001 | t0041 | g0125 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18992 | hp1 | a0001 | c0002 | t0005 | g0072 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18993 | hp2 | a0001 | c0002 | t0051 | g0024 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19002 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19004 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19004 | hp2 | a0007 | c0015 | t0001 | g0128 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19011 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19012 | hp1 | a0001 | c0002 | t0005 | g0080 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19030 | hp1 | a0001 | c0004 | t0014 | g0062 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19030 | hp2 | a0001 | c0001 | t0030 | g0244 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19043 | hp2 | a0001 | c0001 | t0039 | g0242 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19056 | hp2 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19057 | hp2 | a0001 | c0002 | t0026 | g0076 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19063 | hp2 | a0001 | c0002 | t0005 | g0070 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19075 | hp1 | a0001 | c0002 | t0005 | g0073 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19075 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19076 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19077 | hp1 | a0001 | c0001 | t0035 | g0112 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19081 | hp1 | a0001 | c0013 | t0009 | g0007 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19081 | hp2 | a0001 | c0001 | t0020 | g0010 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20129 | hp1 | a0001 | c0001 | t0019 | g0227 | AFR | ASW | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0058 | AFR | ASW | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0041 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20905 | hp1 | a0001 | c0001 | t0013 | g0011 | SAS | GIH | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20905 | hp2 | a0001 | c0001 | t0050 | g0147 | SAS | GIH | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02109 | hp1 | a0001 | c0001 | t0047 | g0086 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02109 | hp2 | a0001 | c0014 | t0037 | g0065 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02486 | hp2 | a0001 | c0001 | t0018 | g0089 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02559 | hp1 | a0001 | c0001 | t0040 | g0216 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG02559 | hp2 | a0001 | c0018 | t0031 | g0055 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG03471 | hp2 | a0001 | c0001 | t0044 | g0172 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG06807 | hp1 | a0001 | c0002 | t0018 | g0068 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
HG06807 | hp2 | a0001 | c0001 | t0017 | g0023 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
NA21309 | hp2 | a0001 | c0002 | t0053 | g0071 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0011 | REF | REF | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0055 | g0067 | REF | REF | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:5187938 | C | T | 1 | a0003 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.133C>T | p.Arg45Cys | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 232/6113 | 133/1974 | 45/657 | chr3 | 5187938 | ||
chr3:5195222 | A | G | 1 | a0007 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.523A>G | p.Ile175Val | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/12 | 622/6113 | 523/1974 | 175/657 | chr3 | 5195222 | ||
chr3:5202993 | G | A | 1 | a0002 | 8 | HG00438.hp1 HG02071.hp1 NA18943.hp2 others(5): Show |
missense_variant | MODERATE | c.886G>A | p.Asp296Asn | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/12 | 985/6113 | 886/1974 | 296/657 | chr3 | 5202993 | ||
chr3:5207202 | G | A | 1 | a0004 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1267G>A | p.Val423Met | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/12 | 1366/6113 | 1267/1974 | 423/657 | chr3 | 5207202 | ||
chr3:5213410 | G | A | 1 | a0006 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1772G>A | p.Arg591Gln | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1871/6113 | 1772/1974 | 591/657 | chr3 | 5213410 | ||
chr3:5213410 | G | C | 1 | a0005 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.1772G>C | p.Arg591Pro | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1871/6113 | 1772/1974 | 591/657 | chr3 | 5213410 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:5187922 | C | G | 1 | a0001c0018 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.117C>G | p.Leu39Leu | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 216/6113 | 117/1974 | 39/657 | chr3 | 5187922 | ||
chr3:5187958 | C | T | 1 | a0001c0005 | 3 | HG01256.hp2 HG02451.hp2 HG02738.hp2 |
synonymous_variant | LOW | c.153C>T | p.Gly51Gly | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 252/6113 | 153/1974 | 51/657 | chr3 | 5187958 | ||
chr3:5187967 | G | A | 1 | a0001c0006 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.162G>A | p.Ser54Ser | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 261/6113 | 162/1974 | 54/657 | chr3 | 5187967 | ||
chr3:5188138 | G | A | 1 | a0001c0007 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.333G>A | p.Pro111Pro | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 432/6113 | 333/1974 | 111/657 | chr3 | 5188138 | ||
chr3:5188222 | C | T | 1 | a0001c0016 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.417C>T | p.Val139Val | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 516/6113 | 417/1974 | 139/657 | chr3 | 5188222 | ||
chr3:5199618 | G | A | 1 | a0001c0008 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.609G>A | p.Gln203Gln | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/12 | 708/6113 | 609/1974 | 203/657 | chr3 | 5199618 | ||
chr3:5199624 | C | A | 17 | a0001c0001a0001c0004a0001c0005others(14): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
synonymous_variant | LOW | c.615C>A | p.Ala205Ala | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/12 | 714/6113 | 615/1974 | 205/657 | chr3 | 5199624 | ||
chr3:5201870 | G | A | 1 | a0001c0004 | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
synonymous_variant | LOW | c.804G>A | p.Ala268Ala | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/12 | 903/6113 | 804/1974 | 268/657 | chr3 | 5201870 | ||
chr3:5211129 | C | T | 3 | a0001c0004a0001c0014a0001c0018 | 7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.1593C>T | p.Tyr531Tyr | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/12 | 1692/6113 | 1593/1974 | 531/657 | chr3 | 5211129 | ||
chr3:5213492 | T | C | 1 | a0001c0012 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1854T>C | p.His618His | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1953/6113 | 1854/1974 | 618/657 | chr3 | 5213492 | ||
chr3:5213522 | C | T | 1 | a0001c0013 | 1 | NA19081.hp1 | splice_region_variant&synonymous_variant | LOW | c.1884C>T | p.Asn628Asn | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1983/6113 | 1884/1974 | 628/657 | chr3 | 5213522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:5187738 | C | A | 2 | a0001c0001t0021a0001c0001t0027 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-68C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 68 | chr3 | 5187738 | |||||
chr3:5187746 | G | A | 2 | a0001c0001t0021a0001c0001t0027 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-60G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 60 | chr3 | 5187746 | |||||
chr3:5187749 | G | A | 1 | a0001c0007t0028 | 1 | HG03942.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | chr3 | 5187749 | ||||||
chr3:5187764 | G | T | 1 | a0001c0001t0062 | 1 | NA18961.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 42 | chr3 | 5187764 | |||||
chr3:5187771 | C | T | 1 | a0001c0001t0061 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 35 | chr3 | 5187771 | |||||
chr3:5216059 | G | A | 2 | a0001c0004t0014a0001c0004t0029 | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 141 | chr3 | 5216059 | |||||
chr3:5216108 | T | C | 1 | a0001c0001t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*190T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 190 | chr3 | 5216108 | |||||
chr3:5216163 | T | C | 1 | a0001c0018t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 245 | chr3 | 5216163 | |||||
chr3:5216224 | A | G | 1 | a0001c0001t0060 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*306A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 306 | chr3 | 5216224 | |||||
chr3:5216283 | T | C | 1 | a0001c0001t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 365 | chr3 | 5216283 | |||||
chr3:5216286 | C | T | 7 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(4): Show | 24 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*368C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 368 | chr3 | 5216286 | |||||
chr3:5216290 | A | T | 7 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(4): Show | 24 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*372A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 372 | chr3 | 5216290 | |||||
chr3:5216296 | T | A | 7 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(4): Show | 24 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 378 | chr3 | 5216296 | |||||
chr3:5216393 | G | A | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 475 | chr3 | 5216393 | |||||
chr3:5216505 | T | G | 3 | a0001c0004t0014a0001c0004t0029a0001c0014t0037 | 6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*587T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 587 | chr3 | 5216505 | |||||
chr3:5216551 | G | C | 14 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(11): Show | 36 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*633G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 633 | chr3 | 5216551 | |||||
chr3:5216571 | C | T | 1 | a0001c0001t0036 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*653C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 653 | chr3 | 5216571 | |||||
chr3:5216595 | A | G | 7 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(4): Show | 24 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*677A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 677 | chr3 | 5216595 | |||||
chr3:5216746 | G | A | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*828G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 828 | chr3 | 5216746 | |||||
chr3:5216879 | T | C | 1 | a0001c0001t0048 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*961T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 961 | chr3 | 5216879 | |||||
chr3:5216887 | C | A | 3 | a0001c0001t0018a0001c0001t0061a0001c0002t0018 | 4 | HG02486.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*969C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 969 | chr3 | 5216887 | |||||
chr3:5217061 | A | G | 3 | a0001c0004t0014a0001c0004t0029a0001c0014t0037 | 6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1143A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1143 | chr3 | 5217061 | |||||
chr3:5217078 | A | T | 3 | a0001c0004t0014a0001c0004t0029a0001c0014t0037 | 6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1160A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1160 | chr3 | 5217078 | |||||
chr3:5217300 | T | C | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*1382T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1382 | chr3 | 5217300 | |||||
chr3:5217513 | A | G | 1 | a0001c0001t0059 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1595A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1595 | chr3 | 5217513 | |||||
chr3:5217549 | A | G | 2 | a0001c0001t0021a0001c0001t0027 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1631A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1631 | chr3 | 5217549 | |||||
chr3:5217737 | T | C | 1 | a0001c0001t0017 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1819T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1819 | chr3 | 5217737 | |||||
chr3:5217782 | T | C | 1 | a0001c0001t0040 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1864T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1864 | chr3 | 5217782 | |||||
chr3:5217795 | T | A | 7 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(4): Show | 24 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1877T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1877 | chr3 | 5217795 | |||||
chr3:5217878 | T | C | 2 | a0001c0004t0014a0001c0004t0029 | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1960T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1960 | chr3 | 5217878 | |||||
chr3:5217908 | G | A | 13 | a0001c0001t0005a0001c0001t0012a0001c0001t0016others(10): Show | 37 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1990G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1990 | chr3 | 5217908 | |||||
chr3:5217939 | C | T | 1 | a0001c0014t0037 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2021C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2021 | chr3 | 5217939 | |||||
chr3:5218123 | A | C | 14 | a0001c0001t0005a0001c0001t0012a0001c0001t0016others(11): Show | 38 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2205A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2205 | chr3 | 5218123 | |||||
chr3:5218270 | C | A | 1 | a0001c0012t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2352C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2352 | chr3 | 5218270 | |||||
chr3:5218271 | G | A | 1 | a0001c0004t0014 | 4 | HG02976.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2353G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2353 | chr3 | 5218271 | |||||
chr3:5218323 | G | T | 1 | a0001c0001t0057 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2405G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2405 | chr3 | 5218323 | |||||
chr3:5218353 | G | GT | 4 | a0001c0001t0011a0001c0001t0035a0001c0001t0039others(1): Show | 8 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2453dupT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2454 | INFO_REALIGN_3_PRIME | chr3 | 5218353 | ||||
chr3:5218353 | GT | G | 8 | a0001c0001t0015a0001c0001t0017a0001c0001t0038others(5): Show | 16 | HG01243.hp1 HG01515.hp1 HG01515.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2453delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2453 | INFO_REALIGN_3_PRIME | chr3 | 5218353 | ||||
chr3:5218353 | GTT | G | 15 | a0001c0001t0005a0001c0001t0012a0001c0001t0016others(12): Show | 38 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2452_*2453delTT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2452 | INFO_REALIGN_3_PRIME | chr3 | 5218353 | ||||
chr3:5218368 | T | C | 1 | a0001c0001t0025 | 2 | HG02027.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2450T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2450 | chr3 | 5218368 | |||||
chr3:5218371 | T | TA | 2 | a0001c0001t0022a0001c0001t0023 | 4 | HG00280.hp2 HG00738.hp2 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2456dupA | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2457 | INFO_REALIGN_3_PRIME | chr3 | 5218371 | ||||
chr3:5218427 | T | C | 1 | a0001c0002t0051 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2509T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2509 | chr3 | 5218427 | |||||
chr3:5218445 | A | C | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*2527A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2527 | chr3 | 5218445 | |||||
chr3:5218446 | C | A | 13 | a0001c0001t0005a0001c0001t0012a0001c0001t0016others(10): Show | 37 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2528C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2528 | chr3 | 5218446 | |||||
chr3:5218614 | G | A | 40 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(37): Show | 200 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*2696G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2696 | chr3 | 5218614 | |||||
chr3:5218658 | A | G | 1 | a0001c0001t0038 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2740A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2740 | chr3 | 5218658 | |||||
chr3:5218713 | T | A | 2 | a0001c0001t0021a0001c0001t0044 | 3 | HG02055.hp2 HG02622.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2795T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2795 | chr3 | 5218713 | |||||
chr3:5218714 | A | G | 2 | a0001c0001t0021a0001c0001t0044 | 3 | HG02055.hp2 HG02622.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2796A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2796 | chr3 | 5218714 | |||||
chr3:5218759 | T | G | 19 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(16): Show | 79 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2841T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2841 | chr3 | 5218759 | |||||
chr3:5218760 | C | A | 19 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(16): Show | 79 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2842C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2842 | chr3 | 5218760 | |||||
chr3:5218965 | A | G | 1 | a0001c0001t0050 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3047A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3047 | chr3 | 5218965 | |||||
chr3:5219095 | C | T | 1 | a0001c0016t0034 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3177C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3177 | chr3 | 5219095 | |||||
chr3:5219291 | A | G | 1 | a0001c0001t0045 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3373A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3373 | chr3 | 5219291 | |||||
chr3:5219424 | C | T | 1 | a0001c0001t0024 | 2 | HG02647.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3506C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3506 | chr3 | 5219424 | |||||
chr3:5219495 | G | A | 1 | a0001c0001t0046 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3577G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3577 | chr3 | 5219495 | |||||
chr3:5219654 | C | A | 1 | a0001c0012t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3736C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3736 | chr3 | 5219654 | |||||
chr3:5219684 | A | T | 1 | a0001c0012t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3766A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3766 | chr3 | 5219684 | |||||
chr3:5219700 | A | T | 1 | a0001c0001t0052 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3782A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3782 | chr3 | 5219700 | |||||
chr3:5219701 | C | A | 2 | a0001c0001t0012a0001c0001t0052 | 6 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3783C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3783 | chr3 | 5219701 | |||||
chr3:5219709 | A | T | 1 | a0001c0001t0033 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3791A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3791 | chr3 | 5219709 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:5188447 | G | A | 2 | a0001c0001t0002g0021a0001c0001t0003g0021 | 2 | NA18966.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.509+133G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188447 | ||||||
chr3:5188573 | A | T | 1 | a0001c0001t0004g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509+259A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188573 | ||||||
chr3:5188658 | C | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.509+344C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188658 | ||||||
chr3:5188763 | C | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.509+449C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188763 | ||||||
chr3:5188857 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.509+543C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188857 | ||||||
chr3:5188980 | A | C | 3 | a0001c0001t0004g0255a0001c0001t0004g0256a0001c0001t0004g0257 | 3 | HG00544.hp2 NA18962.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.509+666A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188980 | ||||||
chr3:5189012 | C | T | 1 | a0001c0001t0009g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+698C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189012 | ||||||
chr3:5189038 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.509+724C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189038 | ||||||
chr3:5189044 | G | T | 1 | a0001c0002t0005g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.509+730G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189044 | ||||||
chr3:5189072 | C | T | 1 | a0001c0001t0015g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.509+758C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189072 | ||||||
chr3:5189114 | A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0250a0001c0001t0002g0009others(5): Show | 11 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+800A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189114 | ||||||
chr3:5189182 | C | T | 1 | a0001c0001t0011g0247 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.509+868C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189182 | ||||||
chr3:5189352 | G | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.509+1038G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189352 | ||||||
chr3:5189421 | C | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0250a0001c0001t0002g0009others(4): Show | 10 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.509+1107C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189421 | ||||||
chr3:5189692 | T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.509+1378T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189692 | ||||||
chr3:5189749 | T | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(16): Show | 24 | HG00140.hp1 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.509+1435T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189749 | ||||||
chr3:5189793 | G | A | 56 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(53): Show | 61 | HG00544.hp2 HG00558.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.509+1479G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189793 | ||||||
chr3:5189802 | G | C | 1 | a0001c0001t0004g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.509+1488G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189802 | ||||||
chr3:5189942 | A | C | 1 | a0001c0001t0007g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.509+1628A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189942 | ||||||
chr3:5189999 | T | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.509+1685T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189999 | ||||||
chr3:5189999 | TG | T | 50 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(47): Show | 55 | HG00544.hp2 HG00558.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.509+1695delG | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5189999 | |||||
chr3:5190001 | G | A | 1 | a0001c0018t0031g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.509+1687G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190001 | ||||||
chr3:5190002 | G | GT | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.509+1688_509+1689i others(3): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190002 | ||||||
chr3:5190086 | ACAT | A | 100 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(97): Show | 110 | HG00544.hp2 HG00558.hp1 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.509+1776_509+1778d others(5): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5190086 | |||||
chr3:5190141 | T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.509+1827T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190141 | ||||||
chr3:5190290 | T | G | 1 | a0001c0001t0061g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.509+1976T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190290 | ||||||
chr3:5190389 | A | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.509+2075A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190389 | ||||||
chr3:5190395 | C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.509+2081C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190395 | ||||||
chr3:5190464 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.509+2150C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190464 | ||||||
chr3:5190496 | G | A | 8 | a0001c0001t0002g0109a0001c0001t0003g0015a0001c0001t0003g0016others(5): Show | 12 | NA18939.hp1 NA18940.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.509+2182G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190496 | ||||||
chr3:5190545 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.509+2231C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190545 | ||||||
chr3:5190568 | C | T | 1 | a0001c0001t0008g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+2254C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190568 | ||||||
chr3:5190771 | T | G | 5 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0003g0200others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+2457T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190771 | ||||||
chr3:5190804 | C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.509+2490C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190804 | ||||||
chr3:5190836 | C | G | 2 | a0001c0001t0001g0037a0001c0001t0002g0037 | 2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.509+2522C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190836 | ||||||
chr3:5190867 | T | A | 2 | a0001c0001t0002g0095a0001c0001t0016g0056 | 2 | HG02818.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.509+2553T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190867 | ||||||
chr3:5190878 | T | A | 1 | a0001c0001t0009g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+2564T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190878 | ||||||
chr3:5190879 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.509+2565A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190879 | ||||||
chr3:5191224 | TTTTG | T | 6 | a0001c0001t0011g0057a0001c0001t0011g0058a0001c0001t0011g0059others(3): Show | 6 | HG02055.hp1 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+2922_509+2925d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5191224 | |||||
chr3:5191277 | G | T | 1 | a0001c0014t0037g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.509+2963G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191277 | ||||||
chr3:5191390 | AT | A | 6 | a0001c0001t0003g0200a0001c0001t0004g0205a0001c0001t0009g0096others(3): Show | 6 | HG01169.hp1 HG01256.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+3090delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5191390 | |||||
chr3:5191404 | T | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3090T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191404 | ||||||
chr3:5191429 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3115T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191429 | ||||||
chr3:5191494 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3180A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191494 | ||||||
chr3:5191597 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.509+3283G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191597 | ||||||
chr3:5191680 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3366C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191680 | ||||||
chr3:5191689 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3375T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191689 | ||||||
chr3:5191725 | G | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3411G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191725 | ||||||
chr3:5191734 | A | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.509+3420A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191734 | ||||||
chr3:5191777 | G | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3432G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191777 | ||||||
chr3:5191824 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3385T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191824 | ||||||
chr3:5191935 | A | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3274A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191935 | ||||||
chr3:5191973 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3236A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191973 | ||||||
chr3:5191978 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3231A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191978 | ||||||
chr3:5191991 | T | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01516.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.510-3218T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191991 | ||||||
chr3:5192009 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3200G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192009 | ||||||
chr3:5192102 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3107C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192102 | ||||||
chr3:5192112 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.510-3097C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192112 | ||||||
chr3:5192115 | G | C | 1 | a0001c0001t0042g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.510-3094G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192115 | ||||||
chr3:5192118 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3091A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192118 | ||||||
chr3:5192157 | C | T | 1 | a0001c0018t0031g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510-3052C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192157 | ||||||
chr3:5192231 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.510-2978G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192231 | ||||||
chr3:5192355 | C | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-2854C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192355 | ||||||
chr3:5192395 | A | T | 2 | a0001c0001t0030g0244a0001c0001t0039g0242 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-2814A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192395 | ||||||
chr3:5192416 | A | C | 6 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0004t0014g0012others(3): Show | 9 | HG02559.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.510-2793A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192416 | ||||||
chr3:5192746 | T | C | 2 | a0001c0001t0004g0116a0001c0001t0004g0117 | 2 | NA18998.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.510-2463T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192746 | ||||||
chr3:5192812 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-2397A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192812 | ||||||
chr3:5192870 | G | A | 1 | a0001c0001t0008g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-2339G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192870 | ||||||
chr3:5192870 | G | T | 2 | a0001c0001t0030g0244a0001c0001t0039g0242 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-2339G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192870 | ||||||
chr3:5192906 | A | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-2303A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192906 | ||||||
chr3:5192919 | A | G | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.510-2290A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192919 | ||||||
chr3:5193001 | A | G | 1 | a0001c0001t0006g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.510-2208A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193001 | ||||||
chr3:5193041 | A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.510-2168A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193041 | ||||||
chr3:5193211 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1998T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193211 | ||||||
chr3:5193231 | C | G | 1 | a0001c0001t0002g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.510-1978C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193231 | ||||||
chr3:5193247 | G | A | 2 | a0001c0001t0030g0244a0001c0001t0039g0242 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-1962G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193247 | ||||||
chr3:5193310 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1899G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193310 | ||||||
chr3:5193342 | C | G | 1 | a0001c0001t0004g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.510-1867C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193342 | ||||||
chr3:5193567 | T | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1642T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193567 | ||||||
chr3:5193616 | A | G | 3 | a0001c0001t0001g0190a0001c0001t0002g0191a0001c0001t0002g0192 | 3 | HG02717.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.510-1593A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193616 | ||||||
chr3:5193618 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.510-1591A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193618 | ||||||
chr3:5193675 | G | A | 1 | a0001c0001t0003g0105 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.510-1534G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193675 | ||||||
chr3:5193759 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1450A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193759 | ||||||
chr3:5193788 | G | A | 19 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(16): Show | 21 | HG00544.hp2 HG00738.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.510-1421G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193788 | ||||||
chr3:5193822 | T | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1387T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193822 | ||||||
chr3:5193919 | T | G | 1 | a0001c0014t0037g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.510-1290T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193919 | ||||||
chr3:5194112 | G | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1097G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194112 | ||||||
chr3:5194285 | T | A | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.510-924T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194285 | ||||||
chr3:5194313 | T | A | 1 | a0001c0001t0004g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.510-896T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194313 | ||||||
chr3:5194435 | G | C | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.510-774G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194435 | ||||||
chr3:5194435 | G | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-774G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194435 | ||||||
chr3:5194574 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.510-635A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194574 | ||||||
chr3:5194590 | T | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-619T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194590 | ||||||
chr3:5194630 | A | G | 1 | a0001c0005t0009g0114 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.510-579A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194630 | ||||||
chr3:5194655 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-554C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194655 | ||||||
chr3:5194764 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-445C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194764 | ||||||
chr3:5194791 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.510-418G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194791 | ||||||
chr3:5194836 | A | C | 3 | a0001c0001t0030g0244a0001c0001t0038g0060a0001c0001t0039g0242 | 3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-373A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194836 | ||||||
chr3:5194845 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-364T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194845 | ||||||
chr3:5195028 | A | G | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.510-181A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195028 | ||||||
chr3:5195054 | G | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-155G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195054 | ||||||
chr3:5195054 | G | T | 1 | a0001c0001t0023g0251 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.510-155G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195054 | ||||||
chr3:5195122 | C | T | 5 | a0001c0001t0008g0043a0001c0001t0008g0051a0001c0001t0008g0052others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-87C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195122 | ||||||
chr3:5195155 | T | C | 1 | a0001c0002t0018g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.510-54T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195155 | ||||||
chr3:5195293 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.582+12C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195293 | ||||||
chr3:5195301 | T | A | 6 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0004t0014g0012others(3): Show | 9 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.582+20T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195301 | ||||||
chr3:5195305 | A | G | 1 | a0001c0014t0037g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.582+24A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195305 | ||||||
chr3:5195500 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+219G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195500 | ||||||
chr3:5195564 | G | T | 8 | a0001c0001t0002g0003a0001c0001t0002g0186a0001c0001t0002g0187others(5): Show | 14 | HG02056.hp1 HG02083.hp1 HG03704.hp1 others(11): Show |
intron_variant | MODIFIER | c.582+283G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195564 | ||||||
chr3:5195599 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+318T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195599 | ||||||
chr3:5195710 | A | G | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+429A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195710 | ||||||
chr3:5195753 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+472C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195753 | ||||||
chr3:5195793 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+512C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195793 | ||||||
chr3:5195833 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+552C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195833 | ||||||
chr3:5195844 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.582+563G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195844 | ||||||
chr3:5195849 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.582+568C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195849 | ||||||
chr3:5195891 | G | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+610G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195891 | ||||||
chr3:5195976 | T | G | 1 | a0001c0001t0004g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.582+695T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195976 | ||||||
chr3:5196009 | T | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+728T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196009 | ||||||
chr3:5196165 | A | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+884A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196165 | ||||||
chr3:5196192 | C | T | 1 | a0001c0008t0049g0183 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.582+911C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196192 | ||||||
chr3:5196337 | G | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1056G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196337 | ||||||
chr3:5196375 | T | C | 1 | a0001c0001t0003g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.582+1094T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196375 | ||||||
chr3:5196387 | T | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1106T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196387 | ||||||
chr3:5196426 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1145T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196426 | ||||||
chr3:5196427 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.582+1146A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196427 | ||||||
chr3:5196461 | G | GAC | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.582+1202_582+1203d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | |||||
chr3:5196461 | G | GACAC | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0192others(2): Show | 5 | HG00597.hp2 HG02717.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.582+1200_582+1203d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | |||||
chr3:5196461 | G | GACACAC | 3 | a0001c0001t0006g0008a0001c0001t0043g0008a0001c0004t0014g0012 | 8 | HG00423.hp2 HG02080.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.582+1198_582+1203d others(8): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | |||||
chr3:5196461 | G | GACGCACA others(5): Show |
1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1182_582+1183i others(14): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | |||||
chr3:5196483 | C | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1202C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196483 | ||||||
chr3:5196489 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.582+1208T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196489 | ||||||
chr3:5196565 | A | G | 1 | a0001c0001t0003g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.582+1284A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196565 | ||||||
chr3:5196664 | A | G | 9 | a0001c0001t0002g0036a0001c0001t0002g0173a0001c0001t0002g0174others(6): Show | 9 | HG00140.hp2 HG00280.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.582+1383A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196664 | ||||||
chr3:5196856 | CA | C | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1577delA | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196856 | |||||
chr3:5196904 | A | G | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1623A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196904 | ||||||
chr3:5196913 | GTCTTT | G | 13 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0028others(10): Show | 18 | HG00642.hp2 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.582+1654_582+1658d others(7): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196913 | |||||
chr3:5196913 | GTCTTTTC others(3): Show |
G | 3 | a0001c0001t0012g0232a0001c0001t0012g0233a0001c0001t0012g0234 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.582+1649_582+1658d others(12): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196913 | |||||
chr3:5196920 | C | CTT | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.582+1642_582+1643d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196920 | |||||
chr3:5196930 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1649C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196930 | ||||||
chr3:5196935 | C | CT | 7 | a0001c0001t0003g0110a0001c0001t0017g0023a0001c0001t0017g0064others(4): Show | 8 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.582+1668dupT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196935 | |||||
chr3:5196935 | C | T | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1654C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196935 | ||||||
chr3:5196943 | T | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1662T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196943 | ||||||
chr3:5196990 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1709G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196990 | ||||||
chr3:5197019 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.582+1738C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197019 | ||||||
chr3:5197041 | G | A | 73 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(70): Show | 81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.582+1760G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197041 | ||||||
chr3:5197064 | CT | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.582+1801delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5197064 | |||||
chr3:5197064 | CTT | C | 6 | a0001c0001t0004g0020a0001c0001t0004g0038a0001c0001t0004g0259others(3): Show | 8 | HG02257.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.582+1800_582+1801d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5197064 | |||||
chr3:5197082 | T | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.582+1801T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197082 | ||||||
chr3:5197135 | A | G | 8 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0018g0091others(5): Show | 11 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+1854A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197135 | ||||||
chr3:5197420 | T | G | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+2139T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197420 | ||||||
chr3:5197485 | A | G | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.583-2107A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197485 | ||||||
chr3:5197596 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1996T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197596 | ||||||
chr3:5197680 | C | T | 1 | a0001c0001t0015g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.583-1912C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197680 | ||||||
chr3:5197739 | G | T | 1 | a0001c0001t0011g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.583-1853G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197739 | ||||||
chr3:5197855 | C | T | 1 | a0001c0001t0004g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.583-1737C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197855 | ||||||
chr3:5197890 | G | A | 1 | a0001c0001t0007g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583-1702G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197890 | ||||||
chr3:5197924 | A | G | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.583-1668A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197924 | ||||||
chr3:5197943 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1649A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197943 | ||||||
chr3:5198015 | C | T | 2 | a0001c0005t0001g0165a0001c0005t0004g0113 | 2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.583-1577C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198015 | ||||||
chr3:5198052 | CT | C | 14 | a0001c0001t0004g0061a0001c0001t0006g0087a0001c0001t0006g0088others(11): Show | 14 | HG01106.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.583-1530delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198052 | |||||
chr3:5198139 | A | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.583-1453A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198139 | ||||||
chr3:5198204 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1388C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198204 | ||||||
chr3:5198236 | A | G | 1 | a0001c0001t0039g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.583-1356A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198236 | ||||||
chr3:5198295 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.583-1297C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198295 | ||||||
chr3:5198347 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1245C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198347 | ||||||
chr3:5198373 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.583-1219C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198373 | ||||||
chr3:5198654 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-938G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198654 | ||||||
chr3:5198662 | CT | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.583-908delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198662 | |||||
chr3:5198662 | CTT | C | 57 | a0001c0001t0001g0017a0001c0001t0001g0130a0001c0001t0001g0167others(54): Show | 63 | HG00544.hp2 HG00738.hp1 HG01168.hp2 others(60): Show |
intron_variant | MODIFIER | c.583-909_583-908del others(2): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198662 | |||||
chr3:5198662 | CTTT | C | 6 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0003g0175others(3): Show | 6 | HG00280.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.583-910_583-908del others(3): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198662 | |||||
chr3:5198683 | T | C | 1 | a0001c0001t0030g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.583-909T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198683 | ||||||
chr3:5198719 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-873G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198719 | ||||||
chr3:5198747 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-845T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198747 | ||||||
chr3:5198804 | A | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-788A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198804 | ||||||
chr3:5198816 | C | A | 1 | a0001c0001t0001g0031 | 2 | NA18961.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.583-776C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198816 | ||||||
chr3:5198884 | G | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-708G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198884 | ||||||
chr3:5198946 | C | T | 3 | a0001c0001t0030g0244a0001c0001t0038g0060a0001c0001t0039g0242 | 3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.583-646C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198946 | ||||||
chr3:5198950 | G | A | 6 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0004t0014g0012others(3): Show | 9 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.583-642G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198950 | ||||||
chr3:5199043 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.583-549C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199043 | ||||||
chr3:5199069 | A | G | 1 | a0001c0001t0004g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.583-523A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199069 | ||||||
chr3:5199100 | T | A | 1 | a0001c0018t0031g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.583-492T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199100 | ||||||
chr3:5199416 | A | T | 10 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0021g0093others(7): Show | 11 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.583-176A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199416 | ||||||
chr3:5199437 | G | T | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-155G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199437 | ||||||
chr3:5199514 | C | T | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.583-78C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199514 | ||||||
chr3:5199538 | C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.583-54C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199538 | ||||||
chr3:5199783 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+88A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5199783 | ||||||
chr3:5199905 | C | T | 8 | a0001c0001t0004g0199a0001c0001t0004g0205a0001c0001t0004g0222others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.686+210C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5199905 | ||||||
chr3:5199910 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.686+215G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5199910 | ||||||
chr3:5199940 | CT | C | 14 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0003g0203others(11): Show | 16 | HG01168.hp2 HG01256.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+262delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 5199940 | |||||
chr3:5200000 | A | G | 2 | a0001c0001t0002g0162a0001c0001t0038g0060 | 2 | HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.686+305A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200000 | ||||||
chr3:5200060 | A | T | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+365A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200060 | ||||||
chr3:5200125 | T | G | 62 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(59): Show | 70 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.686+430T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200125 | ||||||
chr3:5200151 | C | T | 1 | a0001c0001t0041g0125 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.686+456C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200151 | ||||||
chr3:5200174 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.686+479C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200174 | ||||||
chr3:5200240 | G | A | 16 | a0001c0001t0001g0004a0001c0001t0002g0004a0001c0001t0002g0021others(13): Show | 20 | HG00597.hp1 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.686+545G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200240 | ||||||
chr3:5200297 | T | A | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.686+602T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200297 | ||||||
chr3:5200316 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+621T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200316 | ||||||
chr3:5200459 | C | T | 1 | a0001c0002t0026g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.686+764C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200459 | ||||||
chr3:5200534 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+839T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200534 | ||||||
chr3:5200719 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+1024A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200719 | ||||||
chr3:5200852 | G | A | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.687-901G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200852 | ||||||
chr3:5200891 | A | C | 1 | a0001c0001t0002g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.687-862A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200891 | ||||||
chr3:5201011 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.687-742C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201011 | ||||||
chr3:5201071 | T | C | 1 | a0001c0001t0004g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.687-682T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201071 | ||||||
chr3:5201103 | G | A | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-650G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201103 | ||||||
chr3:5201199 | A | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.687-554A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201199 | ||||||
chr3:5201225 | G | A | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.687-528G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201225 | ||||||
chr3:5201250 | A | G | 1 | a0001c0001t0002g0137 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.687-503A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201250 | ||||||
chr3:5201258 | G | A | 6 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0004t0014g0012others(3): Show | 9 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.687-495G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201258 | ||||||
chr3:5201313 | G | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.687-440G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201313 | ||||||
chr3:5201316 | G | C | 1 | a0001c0001t0001g0014 | 3 | HG02071.hp2 NA18944.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.687-437G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201316 | ||||||
chr3:5201381 | C | T | 1 | a0001c0001t0035g0112 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.687-372C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201381 | ||||||
chr3:5201393 | G | C | 1 | a0001c0005t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.687-360G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201393 | ||||||
chr3:5201430 | G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.687-323G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201430 | ||||||
chr3:5201481 | A | G | 3 | a0001c0001t0030g0244a0001c0001t0038g0060a0001c0001t0039g0242 | 3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.687-272A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201481 | ||||||
chr3:5201497 | C | A | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-256C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201497 | ||||||
chr3:5201594 | A | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.687-159A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201594 | ||||||
chr3:5201721 | T | C | 2 | a0001c0001t0001g0017a0001c0001t0015g0017 | 3 | HG02976.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.687-32T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201721 | ||||||
chr3:5202120 | A | G | 1 | a0001c0004t0029g0063 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.858+196A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202120 | ||||||
chr3:5202171 | G | A | 2 | a0001c0002t0005g0246a0001c0002t0020g0245 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.858+247G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202171 | ||||||
chr3:5202227 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.858+303C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202227 | ||||||
chr3:5202396 | G | A | 1 | a0001c0001t0003g0138 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.858+472G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202396 | ||||||
chr3:5202400 | G | C | 1 | a0001c0002t0018g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.858+476G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202400 | ||||||
chr3:5202559 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-407T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202559 | ||||||
chr3:5202587 | G | A | 5 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0004t0014g0012others(2): Show | 8 | HG02572.hp1 HG02886.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.859-379G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202587 | ||||||
chr3:5202700 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.859-266G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202700 | ||||||
chr3:5202729 | C | G | 3 | a0001c0004t0014g0012a0001c0004t0014g0062a0001c0004t0029g0063 | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-237C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202729 | ||||||
chr3:5202737 | T | C | 3 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0018t0031g0055 | 4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-229T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202737 | ||||||
chr3:5202861 | G | A | 8 | a0001c0001t0004g0199a0001c0001t0004g0205a0001c0001t0004g0222others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.859-105G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202861 | ||||||
chr3:5202906 | C | G | 1 | a0001c0001t0006g0228 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.859-60C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202906 | ||||||
chr3:5203170 | A | G | 1 | a0001c0018t0031g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1042+21A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203170 | ||||||
chr3:5203224 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+75C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203224 | ||||||
chr3:5203254 | A | G | 5 | a0001c0001t0002g0109a0001c0001t0003g0016a0001c0001t0003g0105others(2): Show | 7 | NA18940.hp2 NA18956.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042+105A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203254 | ||||||
chr3:5203418 | C | T | 3 | a0001c0001t0007g0224a0001c0001t0007g0229a0001c0012t0058g0111 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1042+269C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203418 | ||||||
chr3:5203461 | T | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0037others(74): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1042+312T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203461 | ||||||
chr3:5203564 | G | A | 11 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1042+415G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203564 | ||||||
chr3:5203618 | T | C | 2 | a0001c0001t0050g0147a0001c0008t0049g0183 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1042+469T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203618 | ||||||
chr3:5203775 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+626T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203775 | ||||||
chr3:5203844 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+695A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203844 | ||||||
chr3:5203951 | C | G | 1 | a0001c0001t0001g0031 | 2 | NA18961.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1042+802C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203951 | ||||||
chr3:5204072 | A | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+923A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204072 | ||||||
chr3:5204200 | C | T | 1 | a0001c0001t0011g0058 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1043-867C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204200 | ||||||
chr3:5204298 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1043-769G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204298 | ||||||
chr3:5204306 | C | T | 1 | a0001c0002t0020g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1043-761C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204306 | ||||||
chr3:5204341 | T | C | 1 | a0001c0002t0053g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1043-726T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204341 | ||||||
chr3:5204373 | CT | C | 8 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0038g0060others(5): Show | 11 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1043-683delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr3 | 5204373 | |||||
chr3:5204386 | T | G | 1 | a0001c0001t0002g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1043-681T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204386 | ||||||
chr3:5204410 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1043-657A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204410 | ||||||
chr3:5204474 | A | G | 1 | a0001c0001t0003g0035 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1043-593A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204474 | ||||||
chr3:5204481 | C | T | 73 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0208others(70): Show | 81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1043-586C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204481 | ||||||
chr3:5204607 | G | C | 1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1043-460G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204607 | ||||||
chr3:5204612 | G | A | 4 | a0001c0004t0014g0012a0001c0004t0014g0062a0001c0004t0029g0063others(1): Show | 6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1043-455G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204612 | ||||||
chr3:5204681 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1043-386C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204681 | ||||||
chr3:5204775 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1043-292G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204775 | ||||||
chr3:5204844 | A | T | 1 | a0001c0001t0030g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1043-223A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204844 | ||||||
chr3:5204861 | A | G | 1 | a0001c0002t0005g0080 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1043-206A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204861 | ||||||
chr3:5204942 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1043-125C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204942 | ||||||
chr3:5205011 | T | C | 14 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0021g0093others(11): Show | 17 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1043-56T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5205011 | ||||||
chr3:5205027 | G | GT | 3 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0018t0031g0055 | 4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043-40_1043-39ins others(1): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5205027 | ||||||
chr3:5205426 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+185A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205426 | ||||||
chr3:5205531 | C | T | 2 | a0001c0001t0006g0215a0001c0001t0006g0220 | 2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1217+290C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205531 | ||||||
chr3:5205543 | T | G | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1217+302T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205543 | ||||||
chr3:5205586 | A | G | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1217+345A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205586 | ||||||
chr3:5205647 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+406T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205647 | ||||||
chr3:5205703 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+462T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205703 | ||||||
chr3:5205848 | A | G | 1 | a0001c0001t0059g0047 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1217+607A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205848 | ||||||
chr3:5205855 | G | A | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1217+614G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205855 | ||||||
chr3:5205875 | C | G | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+634C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205875 | ||||||
chr3:5205876 | G | A | 1 | a0001c0001t0004g0207 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1217+635G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205876 | ||||||
chr3:5205877 | T | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+636T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205877 | ||||||
chr3:5205881 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+640G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205881 | ||||||
chr3:5205890 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+649G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205890 | ||||||
chr3:5206020 | A | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+779A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206020 | ||||||
chr3:5206028 | C | T | 4 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+787C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206028 | ||||||
chr3:5206071 | A | G | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1217+830A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206071 | ||||||
chr3:5206129 | T | G | 14 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0021g0093others(11): Show | 17 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1217+888T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206129 | ||||||
chr3:5206162 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1217+921G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206162 | ||||||
chr3:5206220 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-933T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206220 | ||||||
chr3:5206221 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-932T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206221 | ||||||
chr3:5206311 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-842G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206311 | ||||||
chr3:5206311 | G | C | 1 | a0001c0001t0003g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1218-842G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206311 | ||||||
chr3:5206318 | C | T | 1 | a0001c0001t0003g0035 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1218-835C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206318 | ||||||
chr3:5206357 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-796A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206357 | ||||||
chr3:5206458 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-695G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206458 | ||||||
chr3:5206594 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-559G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206594 | ||||||
chr3:5206681 | T | G | 1 | a0001c0001t0005g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1218-472T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206681 | ||||||
chr3:5206682 | G | C | 1 | a0001c0001t0005g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1218-471G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206682 | ||||||
chr3:5206683 | C | T | 1 | a0001c0001t0005g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1218-470C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206683 | ||||||
chr3:5206706 | T | G | 1 | a0001c0001t0006g0228 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1218-447T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206706 | ||||||
chr3:5206719 | C | A | 3 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0018t0031g0055 | 4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-434C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206719 | ||||||
chr3:5206801 | C | A | 1 | a0001c0001t0002g0032 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1218-352C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206801 | ||||||
chr3:5206878 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-275A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206878 | ||||||
chr3:5206932 | A | G | 3 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0018t0031g0055 | 4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-221A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206932 | ||||||
chr3:5206962 | A | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-191A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206962 | ||||||
chr3:5206969 | T | C | 1 | a0001c0018t0031g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1218-184T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206969 | ||||||
chr3:5206991 | T | G | 1 | a0001c0001t0006g0019 | 3 | HG03579.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1218-162T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206991 | ||||||
chr3:5207014 | T | G | 2 | a0001c0001t0017g0023a0001c0001t0017g0064 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1218-139T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207014 | ||||||
chr3:5207039 | G | A | 1 | a0001c0001t0004g0122 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1218-114G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207039 | ||||||
chr3:5207040 | A | G | 1 | a0001c0001t0004g0122 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1218-113A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207040 | ||||||
chr3:5207041 | G | A | 1 | a0001c0001t0004g0122 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1218-112G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207041 | ||||||
chr3:5207062 | G | A | 12 | a0001c0001t0002g0191a0001c0001t0017g0023a0001c0001t0017g0064others(9): Show | 15 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1218-91G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207062 | ||||||
chr3:5207144 | G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0038a0001c0001t0004g0259others(2): Show | 7 | HG02257.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-9G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207144 | ||||||
chr3:5207355 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1338+82G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207355 | ||||||
chr3:5207551 | G | T | 1 | a0001c0002t0005g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1338+278G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207551 | ||||||
chr3:5207665 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1338+392T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207665 | ||||||
chr3:5207696 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1339-397C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207696 | ||||||
chr3:5207705 | A | C | 32 | a0001c0001t0006g0193a0001c0001t0008g0053a0001c0001t0021g0093others(29): Show | 34 | HG00558.hp1 HG01109.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1339-388A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207705 | ||||||
chr3:5207713 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1339-380G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207713 | ||||||
chr3:5207826 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-267A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207826 | ||||||
chr3:5207855 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-238C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207855 | ||||||
chr3:5207905 | A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1339-188A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207905 | ||||||
chr3:5208052 | G | A | 2 | a0001c0002t0005g0072a0001c0002t0005g0073 | 2 | NA18992.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1339-41G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5208052 | ||||||
chr3:5208060 | A | G | 1 | a0001c0001t0002g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1339-33A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5208060 | ||||||
chr3:5208277 | GT | G | 10 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(7): Show | 13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1509+27delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208277 | |||||
chr3:5208280 | T | G | 1 | a0001c0018t0031g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1509+17T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208280 | ||||||
chr3:5208600 | T | C | 1 | a0001c0001t0005g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1509+337T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208600 | ||||||
chr3:5208665 | A | C | 1 | a0001c0001t0005g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1509+402A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208665 | ||||||
chr3:5208743 | T | G | 3 | a0001c0001t0001g0027a0001c0001t0015g0027a0001c0012t0058g0111 | 3 | HG01515.hp1 HG01517.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1509+480T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208743 | ||||||
chr3:5208743 | T | TTG | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0004g0257 | 3 | HG00544.hp2 HG00597.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1509+496_1509+497d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208743 | |||||
chr3:5208757 | G | GTA | 3 | a0001c0004t0014g0012a0001c0004t0014g0062a0001c0014t0037g0065 | 5 | HG02109.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+495_1509+496i others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208757 | |||||
chr3:5208759 | G | A | 5 | a0001c0001t0030g0244a0001c0001t0039g0242a0001c0004t0014g0012others(2): Show | 7 | HG02109.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+496G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208759 | ||||||
chr3:5208768 | T | TAC | 6 | a0001c0001t0012g0039a0001c0001t0012g0232a0001c0001t0012g0233others(3): Show | 7 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+506_1509+507i others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208768 | |||||
chr3:5208770 | T | C | 8 | a0001c0001t0012g0039a0001c0001t0012g0232a0001c0001t0012g0233others(5): Show | 9 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+507T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208770 | ||||||
chr3:5208770 | T | TAC | 8 | a0001c0001t0004g0239a0001c0001t0008g0053a0001c0001t0017g0023others(5): Show | 9 | HG00408.hp1 HG01433.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+525_1509+526d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208770 | |||||
chr3:5208770 | TAC | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0098others(2): Show | 8 | HG00642.hp2 HG01168.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1509+525_1509+526d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208770 | |||||
chr3:5208772 | C | T | 5 | a0001c0001t0038g0060a0001c0004t0014g0012a0001c0004t0014g0062others(2): Show | 7 | HG01243.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+509C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208772 | ||||||
chr3:5208790 | T | C | 1 | a0001c0001t0008g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1509+527T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208790 | ||||||
chr3:5209039 | C | T | 4 | a0001c0001t0004g0255a0001c0001t0004g0256a0001c0001t0004g0257others(1): Show | 4 | HG00544.hp2 HG02523.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+776C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209039 | ||||||
chr3:5209040 | T | C | 2 | a0001c0001t0002g0249a0001c0001t0003g0105 | 2 | NA18984.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1509+777T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209040 | ||||||
chr3:5209429 | G | T | 1 | a0001c0001t0004g0257 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1510-746G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209429 | ||||||
chr3:5209617 | G | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0141a0001c0001t0001g0169others(2): Show | 6 | HG00544.hp1 HG02129.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-558G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209617 | ||||||
chr3:5209676 | G | A | 8 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0038g0060others(5): Show | 11 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1510-499G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209676 | ||||||
chr3:5209755 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-420C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209755 | ||||||
chr3:5209779 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-396C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209779 | ||||||
chr3:5209799 | T | C | 10 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(7): Show | 13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1510-376T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209799 | ||||||
chr3:5209882 | A | G | 1 | a0001c0001t0009g0096 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1510-293A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209882 | ||||||
chr3:5209930 | A | G | 1 | a0001c0004t0014g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1510-245A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209930 | ||||||
chr3:5209972 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-203A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209972 | ||||||
chr3:5210098 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-77C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5210098 | ||||||
chr3:5210394 | G | A | 1 | a0001c0001t0023g0251 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1583+146G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210394 | ||||||
chr3:5210428 | C | G | 1 | a0001c0001t0056g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1583+180C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210428 | ||||||
chr3:5210463 | G | T | 2 | a0001c0001t0025g0212a0001c0001t0025g0213 | 2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1583+215G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210463 | ||||||
chr3:5210491 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1583+243T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210491 | ||||||
chr3:5210505 | C | T | 5 | a0001c0004t0014g0012a0001c0004t0014g0062a0001c0004t0029g0063others(2): Show | 7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1583+257C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210505 | ||||||
chr3:5210634 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1583+386A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210634 | ||||||
chr3:5210655 | A | G | 1 | a0001c0001t0009g0146 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1583+407A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210655 | ||||||
chr3:5210673 | A | G | 1 | a0001c0002t0005g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1583+425A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210673 | ||||||
chr3:5210714 | GT | G | 10 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(7): Show | 13 | HG01243.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1584-395delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 5210714 | |||||
chr3:5210725 | T | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-395T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210725 | ||||||
chr3:5210750 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1584-370A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210750 | ||||||
chr3:5210831 | C | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-289C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210831 | ||||||
chr3:5210842 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-278G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210842 | ||||||
chr3:5210904 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-216C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210904 | ||||||
chr3:5210996 | A | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-124A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210996 | ||||||
chr3:5211006 | A | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-114A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5211006 | ||||||
chr3:5211103 | A | G | 11 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1584-17A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5211103 | ||||||
chr3:5211251 | A | T | 1 | a0001c0005t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1680+35A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211251 | ||||||
chr3:5211295 | G | A | 11 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1680+79G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211295 | ||||||
chr3:5211315 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+99T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211315 | ||||||
chr3:5211349 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+133G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211349 | ||||||
chr3:5211350 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1680+134C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211350 | ||||||
chr3:5211388 | T | G | 1 | a0001c0001t0061g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1680+172T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211388 | ||||||
chr3:5211472 | T | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+256T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211472 | ||||||
chr3:5211651 | TGA | T | 6 | a0001c0001t0030g0244a0001c0001t0038g0060a0001c0004t0014g0012others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1680+437_1680+438d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211651 | |||||
chr3:5211653 | A | AGT | 25 | a0001c0001t0004g0199a0001c0001t0005g0121a0001c0001t0006g0193others(22): Show | 27 | HG00558.hp1 HG01109.hp1 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.1680+472_1680+473d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211653 | |||||
chr3:5211653 | A | T | 1 | a0001c0002t0005g0246 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1680+437A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211653 | ||||||
chr3:5211653 | AGT | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1680+472_1680+473d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211653 | |||||
chr3:5211653 | AGTGT | A | 3 | a0001c0001t0002g0191a0001c0001t0017g0023a0001c0001t0017g0064 | 4 | HG02886.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1680+470_1680+473d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211653 | |||||
chr3:5211676 | G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1680+460G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211676 | ||||||
chr3:5211721 | C | G | 1 | a0001c0001t0002g0188 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1680+505C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211721 | ||||||
chr3:5211794 | G | A | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1680+578G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211794 | ||||||
chr3:5211869 | C | T | 1 | a0001c0001t0005g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1680+653C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211869 | ||||||
chr3:5211876 | T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1680+660T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211876 | ||||||
chr3:5211884 | C | T | 1 | a0001c0002t0005g0079 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1680+668C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211884 | ||||||
chr3:5211890 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+674C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211890 | ||||||
chr3:5211901 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+685A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211901 | ||||||
chr3:5211985 | G | A | 14 | a0001c0001t0001g0004a0001c0001t0002g0004a0001c0001t0002g0021others(11): Show | 18 | HG00597.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1680+769G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211985 | ||||||
chr3:5212146 | G | A | 6 | a0001c0001t0002g0109a0001c0001t0003g0015a0001c0001t0003g0016others(3): Show | 10 | NA18939.hp1 NA18940.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.1680+930G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212146 | ||||||
chr3:5212239 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+1023C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212239 | ||||||
chr3:5212308 | C | T | 1 | a0001c0001t0008g0022 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1681-1011C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212308 | ||||||
chr3:5212362 | T | A | 1 | a0001c0001t0015g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1681-957T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212362 | ||||||
chr3:5212470 | A | G | 10 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(7): Show | 13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1681-849A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212470 | ||||||
chr3:5212639 | A | G | 1 | a0001c0001t0006g0215 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1681-680A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212639 | ||||||
chr3:5212708 | G | C | 3 | a0001c0001t0021g0093a0001c0001t0021g0094a0001c0001t0027g0092 | 3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1681-611G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212708 | ||||||
chr3:5212708 | G | T | 1 | a0001c0001t0013g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1681-611G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212708 | ||||||
chr3:5212770 | T | A | 8 | a0001c0001t0004g0199a0001c0001t0004g0205a0001c0001t0004g0222others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-549T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212770 | ||||||
chr3:5212818 | C | T | 10 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(7): Show | 13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1681-501C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212818 | ||||||
chr3:5213000 | A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(249): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1681-319A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213000 | ||||||
chr3:5213051 | T | C | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1681-268T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213051 | ||||||
chr3:5213054 | A | G | 11 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0030g0244others(8): Show | 14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1681-265A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213054 | ||||||
chr3:5213084 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1681-235G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213084 | ||||||
chr3:5213164 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1681-155C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213164 | ||||||
chr3:5213195 | G | C | 1 | a0001c0001t0004g0123 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1681-124G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213195 | ||||||
chr3:5213659 | C | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884+137C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213659 | ||||||
chr3:5213684 | A | G | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884+162A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213684 | ||||||
chr3:5213768 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1884+246G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213768 | ||||||
chr3:5213768 | G | C | 5 | a0001c0001t0001g0197a0001c0001t0006g0215a0001c0001t0006g0220others(2): Show | 7 | HG00408.hp2 HG02896.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884+246G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213768 | ||||||
chr3:5213809 | C | T | 2 | a0001c0001t0001g0144a0001c0001t0002g0145 | 2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1884+287C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213809 | ||||||
chr3:5214033 | G | T | 5 | a0001c0001t0004g0040a0001c0001t0004g0041a0001c0001t0004g0239others(2): Show | 7 | HG00408.hp1 HG00423.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884+511G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214033 | ||||||
chr3:5214107 | T | G | 1 | a0001c0018t0031g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1884+585T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214107 | ||||||
chr3:5214164 | G | A | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884+642G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214164 | ||||||
chr3:5214216 | T | C | 2 | a0001c0001t0001g0151a0001c0001t0015g0166 | 2 | HG02083.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1884+694T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214216 | ||||||
chr3:5214238 | T | C | 6 | a0001c0001t0011g0057a0001c0001t0011g0058a0001c0001t0011g0059others(3): Show | 6 | HG02055.hp1 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1884+716T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214238 | ||||||
chr3:5214305 | C | T | 2 | a0001c0001t0004g0211a0001c0001t0004g0257 | 2 | HG00544.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1884+783C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214305 | ||||||
chr3:5214484 | G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1884+962G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214484 | ||||||
chr3:5214509 | C | T | 1 | a0001c0001t0022g0042 | 2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1884+987C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214509 | ||||||
chr3:5214555 | C | T | 3 | a0001c0001t0030g0244a0001c0001t0038g0060a0001c0001t0039g0242 | 3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1884+1033C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214555 | ||||||
chr3:5214655 | T | G | 7 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0004t0014g0012others(4): Show | 10 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884+1133T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214655 | ||||||
chr3:5214710 | G | C | 6 | a0001c0001t0008g0049a0001c0002t0005g0024a0001c0002t0005g0074others(3): Show | 6 | NA18943.hp1 NA18969.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885-1119G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214710 | ||||||
chr3:5214719 | G | T | 1 | a0001c0001t0002g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1885-1110G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214719 | ||||||
chr3:5214850 | C | T | 1 | a0001c0001t0010g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1885-979C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214850 | ||||||
chr3:5214900 | C | T | 1 | a0001c0001t0019g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1885-929C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214900 | ||||||
chr3:5214995 | C | T | 4 | a0001c0001t0006g0087a0001c0001t0006g0088a0001c0002t0005g0025others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1885-834C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214995 | ||||||
chr3:5215014 | G | C | 16 | a0001c0001t0006g0215a0001c0001t0006g0220a0001c0001t0011g0057others(13): Show | 16 | HG01106.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1885-815G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215014 | ||||||
chr3:5215033 | C | G | 1 | a0001c0001t0003g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1885-796C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215033 | ||||||
chr3:5215034 | A | T | 1 | a0001c0001t0002g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1885-795A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215034 | ||||||
chr3:5215078 | G | A | 1 | a0001c0001t0030g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1885-751G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215078 | ||||||
chr3:5215080 | G | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0182 | 3 | HG01952.hp1 HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1885-749G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215080 | ||||||
chr3:5215097 | A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(242): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1885-732A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215097 | ||||||
chr3:5215099 | G | T | 1 | a0001c0001t0005g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1885-730G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215099 | ||||||
chr3:5215107 | C | T | 3 | a0001c0001t0002g0118a0001c0001t0003g0138a0002c0003t0001g0034 | 4 | NA18964.hp2 NA18975.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1885-722C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215107 | ||||||
chr3:5215171 | G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1885-658G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215171 | ||||||
chr3:5215223 | A | G | 1 | a0001c0001t0040g0216 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1885-606A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215223 | ||||||
chr3:5215271 | G | C | 2 | a0001c0001t0061g0085a0001c0002t0018g0068 | 2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1885-558G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215271 | ||||||
chr3:5215294 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1885-535G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215294 | ||||||
chr3:5215299 | G | A | 2 | a0001c0004t0029g0063a0001c0012t0058g0111 | 2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1885-530G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215299 | ||||||
chr3:5215312 | T | TA | 27 | a0001c0001t0001g0028a0001c0001t0001g0100a0001c0001t0001g0103others(24): Show | 29 | HG00408.hp2 HG00642.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1885-514dupA | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 5215312 | |||||
chr3:5215316 | G | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0100a0001c0001t0001g0103others(24): Show | 29 | HG00408.hp2 HG00642.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1885-513G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215316 | ||||||
chr3:5215341 | T | C | 1 | a0001c0001t0003g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1885-488T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215341 | ||||||
chr3:5215341 | TAGTG | T | 8 | a0001c0001t0004g0199a0001c0001t0004g0205a0001c0001t0004g0222others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1885-484_1885-481d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 5215341 | |||||
chr3:5215345 | G | T | 7 | a0001c0001t0002g0018a0001c0001t0021g0094a0001c0001t0027g0092others(4): Show | 9 | HG00642.hp1 HG01433.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1885-484G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215345 | ||||||
chr3:5215393 | G | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0115a0001c0001t0001g0141others(89): Show | 108 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1885-436G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215393 | ||||||
chr3:5215422 | C | T | 2 | a0001c0001t0006g0215a0001c0001t0006g0220 | 2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1885-407C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215422 | ||||||
chr3:5215430 | G | C | 16 | a0001c0001t0001g0097a0001c0001t0008g0022a0001c0001t0008g0043others(13): Show | 20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1885-399G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215430 | ||||||
chr3:5215463 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1885-366C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215463 | ||||||
chr3:5215464 | G | A | 1 | a0001c0001t0004g0255 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1885-365G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215464 | ||||||
chr3:5215477 | C | T | 2 | a0001c0001t0038g0060a0001c0012t0058g0111 | 2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1885-352C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215477 | ||||||
chr3:5215482 | C | T | 1 | a0001c0012t0058g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1885-347C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215482 | ||||||
chr3:5215491 | T | C | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1885-338T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215491 | ||||||
chr3:5215493 | C | T | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1885-336C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215493 | ||||||
chr3:5215528 | G | A | 1 | a0001c0001t0038g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1885-301G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215528 | ||||||
chr3:5215530 | T | C | 1 | a0001c0001t0039g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1885-299T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215530 | ||||||
chr3:5215690 | G | A | 12 | a0001c0001t0017g0023a0001c0001t0017g0064a0001c0001t0021g0093others(9): Show | 15 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1885-139G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215690 | ||||||
chr3:5215700 | C | T | 2 | a0001c0001t0004g0116a0001c0001t0004g0117 | 2 | NA18998.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1885-129C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215700 | ||||||
chr3:5215729 | T | C | 1 | a0001c0002t0026g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1885-100T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215729 | ||||||
chr3:5215813 | G | A | 2 | a0001c0001t0003g0175a0001c0001t0003g0179 | 2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1885-16G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215813 |