Item | Value |
---|---|
geneid | 121506 |
ensemblid | ENSG00000139055.7 |
hgncid | 26495 |
symbol | ERP27 |
name | endoplasmic reticulum protein 27 |
refseq_nuc | NM_152321.4 |
refseq_prot | NP_689534.1 |
ensembl_nuc | ENST00000266397.7 |
ensembl_prot | ENSP00000266397.2 |
mane_status | MANE Select |
chr | chr12 |
start | 14914039 |
end | 14938537 |
strand | - |
ver | v1.2 |
region | chr12:14914039-14938537 |
region5000 | chr12:14909039-14943537 |
regionname0 | ERP27_chr12_14914039_14938537 |
regionname5000 | ERP27_chr12_14909039_14943537 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 273 | 383 | 91 | 78 | 155 | 16 | 41 | 119 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0002 | 0/0 | 273 | 15 | 0 | 0 | 10 | 0 | 5 | 7 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0003 | 0/0 | 273 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0004 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 822 | 372 | 80 | 78 | 155 | 16 | 41 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
c0002 | 0/0 | 822 | 15 | 0 | 0 | 10 | 0 | 5 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
c0003 | 0/0 | 822 | 11 | 11 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
c0004 | 0/0 | 822 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
c0005 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 730 | 174 | 50 | 38 | 65 | 7 | 13 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0002 | 1/0 | 726 | 80 | 17 | 24 | 26 | 5 | 7 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0003 | 0/0 | 732 | 73 | 0 | 6 | 48 | 1 | 18 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0004 | 0/0 | 730 | 26 | 11 | 1 | 10 | 0 | 4 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0005 | 0/0 | 728 | 9 | 3 | 3 | 1 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0006 | 0/0 | 726 | 9 | 1 | 5 | 1 | 2 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0007 | 0/0 | 732 | 7 | 0 | 0 | 7 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0008 | 0/0 | 730 | 5 | 5 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0009 | 0/0 | 730 | 5 | 0 | 0 | 4 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0010 | 0/0 | 730 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0011 | 0/0 | 724 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0012 | 0/0 | 732 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0013 | 0/0 | 688 | 2 | 0 | 0 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0014 | 0/0 | 728 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0015 | 0/0 | 732 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
t0016 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 2 | 6 | 6 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0002 | 0/0 | 12 | 3 | 2 | 7 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0003 | 0/0 | 8 | 0 | 0 | 5 | 0 | 3 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0004 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0005 | 0/0 | 6 | 0 | 2 | 1 | 2 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0008 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0013 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0050 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
g0289 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 822 | 372 | 80 | 78 | 155 | 16 | 41 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
a0001c0003 | 0/0 | 822 | 11 | 11 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
a0002c0002 | 0/0 | 822 | 15 | 0 | 0 | 10 | 0 | 5 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
a0003c0004 | 0/0 | 822 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 | |
a0004c0005 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1551 | 165 | 42 | 38 | 64 | 7 | 13 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0002 | 1/0 | 1547 | 79 | 17 | 24 | 26 | 5 | 6 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0003 | 0/0 | 1553 | 73 | 0 | 6 | 48 | 1 | 18 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0004 | 0/0 | 1551 | 12 | 11 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0005 | 0/0 | 1549 | 9 | 3 | 3 | 1 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0006 | 0/0 | 1547 | 9 | 1 | 5 | 1 | 2 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0007 | 0/0 | 1553 | 7 | 0 | 0 | 7 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0008 | 0/0 | 1551 | 5 | 5 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0009 | 0/0 | 1551 | 5 | 0 | 0 | 4 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0011 | 0/0 | 1545 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0013 | 0/0 | 1509 | 2 | 0 | 0 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0014 | 0/0 | 1549 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0015 | 0/0 | 1553 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0001t0016 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0003t0001 | 0/0 | 1551 | 8 | 8 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0001c0003t0012 | 0/0 | 1553 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0002c0002t0002 | 0/0 | 1547 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0002c0002t0004 | 0/0 | 1551 | 14 | 0 | 0 | 10 | 0 | 4 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0003c0004t0010 | 0/0 | 1551 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
a0004c0005t0001 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | copy fasta | chr12 | 14909039 | 14943537 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 2 | 6 | 6 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0002 | 0/0 | 12 | 3 | 2 | 7 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0013 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0050 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0004 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0005 | 0/0 | 6 | 0 | 2 | 1 | 2 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0002g0289 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0003 | 0/0 | 8 | 0 | 0 | 5 | 0 | 3 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0007g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0008g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0009g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0009g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0009g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0011g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0013g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0013g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0014g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0015g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0001t0016g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0003t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0003t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0003t0012g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0001c0003t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0002c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0003c0004t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0003c0004t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0003c0004t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
a0004c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0071 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00140 | hp2 | a0001 | c0001 | t0013 | g0088 | EUR | GBR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00544 | hp2 | a0001 | c0001 | t0009 | g0238 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00597 | hp2 | a0001 | c0001 | t0016 | g0223 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0271 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0162 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0156 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0196 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0142 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0151 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01346 | hp2 | a0001 | c0001 | t0015 | g0259 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0163 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02015 | hp2 | a0002 | c0002 | t0004 | g0120 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02027 | hp2 | a0004 | c0005 | t0001 | g0132 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0267 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02083 | hp2 | a0002 | c0002 | t0004 | g0029 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02129 | hp2 | a0001 | c0001 | t0009 | g0229 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02135 | hp1 | a0001 | c0001 | t0011 | g0030 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02145 | hp1 | a0003 | c0004 | t0010 | g0057 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02165 | hp1 | a0002 | c0002 | t0004 | g0123 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CDX | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02258 | hp1 | a0001 | c0003 | t0012 | g0022 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0246 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02886 | hp2 | a0003 | c0004 | t0010 | g0058 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0049 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0111 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0272 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03239 | hp1 | a0001 | c0001 | t0009 | g0147 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03490 | hp2 | a0002 | c0002 | t0004 | g0118 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03491 | hp2 | a0002 | c0002 | t0004 | g0028 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03492 | hp1 | a0002 | c0002 | t0004 | g0122 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03492 | hp2 | a0002 | c0002 | t0004 | g0028 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03579 | hp2 | a0003 | c0004 | t0010 | g0056 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0119 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0235 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04184 | hp1 | a0001 | c0001 | t0013 | g0089 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | BEB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | STU | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18612 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | CHB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18939 | hp2 | a0002 | c0002 | t0004 | g0029 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18945 | hp1 | a0002 | c0002 | t0004 | g0117 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18948 | hp2 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18965 | hp1 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18968 | hp2 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18978 | hp1 | a0002 | c0002 | t0004 | g0124 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18990 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19012 | hp2 | a0002 | c0002 | t0004 | g0121 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0270 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19065 | hp1 | a0001 | c0001 | t0011 | g0030 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19066 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19066 | hp2 | a0002 | c0002 | t0004 | g0201 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19068 | hp1 | a0002 | c0002 | t0004 | g0215 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19075 | hp1 | a0002 | c0002 | t0004 | g0110 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19077 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | YRI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ASW | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20129 | hp2 | a0001 | c0003 | t0012 | g0113 | AFR | ASW | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0239 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0137 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0148 | EUR | TSI | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | GIH | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | GIH | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02486 | hp1 | a0001 | c0003 | t0012 | g0022 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18955 | hp1 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | LWK | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0166 | REF | REF | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0289 | REF | REF | ERP27_chr12_14909039_14943537 | ERP27 | chr12 | 14909039 | 14943537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14917253 | T | C | 1 | a0002 | 15 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(12): Show |
missense_variant | MODERATE | c.501A>G | p.Ile167Met | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/7 | 530/1547 | 501/822 | 167/273 | chr12 | 14917253 | ||
chr12:14917254 | A | G | 1 | a0004 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.500T>C | p.Ile167Thr | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/7 | 529/1547 | 500/822 | 167/273 | chr12 | 14917254 | ||
chr12:14921018 | C | T | 1 | a0003 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.364G>A | p.Glu122Lys | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/7 | 393/1547 | 364/822 | 122/273 | chr12 | 14921018 | ||
chr12:14937993 | A | G | 1 | a0003 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.154T>C | p.Phe52Leu | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/7 | 183/1547 | 154/822 | 52/273 | chr12 | 14937993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14917235 | T | A | 1 | a0001c0003 | 11 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
synonymous_variant | LOW | c.519A>T | p.Pro173Pro | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/7 | 548/1547 | 519/822 | 173/273 | chr12 | 14917235 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14914065 | A | G | 1 | a0001c0001t0015 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 670 | chr12 | 14914065 | |||||
chr12:14914092 | G | T | 1 | a0001c0001t0016 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 643 | chr12 | 14914092 | |||||
chr12:14914195 | C | G | 4 | a0001c0001t0004a0001c0001t0014a0002c0002t0004others(1): Show | 30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*540G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 540 | chr12 | 14914195 | |||||
chr12:14914242 | C | T | 1 | a0001c0001t0008 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*493G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 493 | chr12 | 14914242 | |||||
chr12:14914257 | G | A | 1 | a0001c0003t0012 | 3 | HG02258.hp1 HG02486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*478C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 478 | chr12 | 14914257 | |||||
chr12:14914284 | G | C | 1 | a0003c0004t0010 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*451C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 451 | chr12 | 14914284 | |||||
chr12:14914469 | G | A | 4 | a0001c0001t0004a0001c0001t0014a0002c0002t0004others(1): Show | 30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 266 | chr12 | 14914469 | |||||
chr12:14914531 | C | T | 4 | a0001c0001t0004a0001c0001t0014a0002c0002t0004others(1): Show | 30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 204 | chr12 | 14914531 | |||||
chr12:14914558 | CTG | C | 1 | a0001c0001t0011 | 3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*175_*176delCA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 175 | chr12 | 14914558 | |||||
chr12:14914573 | T | C | 4 | a0001c0001t0004a0001c0001t0014a0002c0002t0004others(1): Show | 30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 162 | chr12 | 14914573 | |||||
chr12:14914575 | T | C | 3 | a0001c0001t0004a0002c0002t0004a0003c0004t0010 | 29 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 160 | chr12 | 14914575 | |||||
chr12:14914575 | TGTGCGTG others(31): Show |
T | 1 | a0001c0001t0013 | 2 | HG00140.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*122_*159delGTGCAC others(32): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 122 | chr12 | 14914575 | |||||
chr12:14914577 | T | C | 2 | a0001c0001t0006a0001c0001t0014 | 10 | HG01081.hp1 HG01106.hp1 HG01261.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*158A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 158 | chr12 | 14914577 | |||||
chr12:14914577 | T | TGC | 1 | a0001c0001t0005 | 9 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*156_*157dupGC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | |||||
chr12:14914577 | T | TGCGC | 2 | a0001c0001t0008a0001c0001t0009 | 10 | HG00544.hp2 HG02055.hp1 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCGC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | |||||
chr12:14914577 | T | TGTGC | 4 | a0001c0001t0001a0001c0001t0016a0001c0003t0001others(1): Show | 175 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | |||||
chr12:14914577 | T | TGTGCGC | 1 | a0001c0001t0007 | 7 | NA18955.hp1 NA18965.hp1 NA19064.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCGCAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | |||||
chr12:14914577 | T | TGTGTGC | 3 | a0001c0001t0003a0001c0001t0015a0001c0003t0012 | 77 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*157_*158insGCACAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 157 | chr12 | 14914577 | |||||
chr12:14914579 | C | CGT | 3 | a0001c0001t0004a0002c0002t0004a0003c0004t0010 | 29 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*154_*155dupAC | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 155 | chr12 | 14914579 | |||||
chr12:14914579 | C | T | 1 | a0001c0001t0014 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*156G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 156 | chr12 | 14914579 | |||||
chr12:14914617 | C | CAT | 4 | a0001c0001t0004a0001c0001t0014a0002c0002t0004others(1): Show | 30 | HG00733.hp1 HG01891.hp1 HG02015.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*117_*118insAT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 7/7 | 117 | chr12 | 14914617 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:14914992 | CT | C | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(55): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.775-211delA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14914992 | ||||||
chr12:14915109 | T | C | 24 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0034others(21): Show | 30 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.775-327A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915109 | ||||||
chr12:14915187 | G | A | 11 | a0001c0001t0004g0060a0001c0001t0004g0061a0001c0001t0004g0102others(8): Show | 11 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.774+302C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915187 | ||||||
chr12:14915213 | A | G | 12 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0110others(9): Show | 14 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.774+276T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915213 | ||||||
chr12:14915381 | C | G | 2 | a0001c0001t0004g0108a0001c0001t0014g0272 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.774+108G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915381 | ||||||
chr12:14915432 | G | T | 1 | a0001c0001t0003g0207 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.774+57C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915432 | ||||||
chr12:14915483 | A | G | 1 | a0001c0001t0003g0239 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.774+6T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 6/6 | chr12 | 14915483 | ||||||
chr12:14915721 | T | C | 19 | a0001c0001t0004g0060a0001c0001t0004g0061a0001c0001t0004g0102others(16): Show | 20 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.577-35A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14915721 | ||||||
chr12:14915754 | T | C | 2 | a0001c0003t0001g0010a0001c0003t0001g0065 | 4 | HG02451.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-68A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14915754 | ||||||
chr12:14916008 | T | G | 5 | a0001c0003t0001g0010a0001c0003t0001g0065a0001c0003t0001g0270others(2): Show | 8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-322A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916008 | ||||||
chr12:14916029 | G | T | 24 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0034others(21): Show | 30 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.577-343C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916029 | ||||||
chr12:14916041 | G | C | 1 | a0001c0001t0006g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.577-355C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916041 | ||||||
chr12:14916068 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.577-382C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916068 | ||||||
chr12:14916324 | C | T | 2 | a0001c0001t0003g0045a0001c0001t0003g0222 | 3 | HG02698.hp2 HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.577-638G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916324 | ||||||
chr12:14916389 | G | A | 17 | a0001c0001t0002g0265a0001c0001t0004g0060a0001c0001t0004g0061others(14): Show | 17 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.577-703C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916389 | ||||||
chr12:14916449 | G | A | 4 | a0001c0001t0001g0195a0001c0001t0002g0093a0001c0001t0002g0178others(1): Show | 4 | HG00423.hp1 HG02155.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+729C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916449 | ||||||
chr12:14916724 | G | A | 1 | a0001c0001t0004g0136 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.576+454C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916724 | ||||||
chr12:14916828 | G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(158): Show | 239 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.576+350C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14916828 | ||||||
chr12:14917015 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.576+163T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14917015 | ||||||
chr12:14917080 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.576+98C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 5/6 | chr12 | 14917080 | ||||||
chr12:14917314 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.451-11C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917314 | ||||||
chr12:14917380 | A | G | 24 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0034others(21): Show | 30 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.451-77T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917380 | ||||||
chr12:14917502 | C | G | 2 | a0001c0001t0003g0204a0001c0001t0003g0212 | 2 | HG00597.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.451-199G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917502 | ||||||
chr12:14917647 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.451-344A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917647 | ||||||
chr12:14917688 | G | A | 12 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0110others(9): Show | 14 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-385C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917688 | ||||||
chr12:14917699 | A | G | 1 | a0001c0001t0003g0191 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.451-396T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917699 | ||||||
chr12:14917701 | C | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(188): Show | 277 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.451-398G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917701 | ||||||
chr12:14917722 | T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.451-419A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917722 | ||||||
chr12:14917741 | T | C | 1 | a0001c0001t0003g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.451-438A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917741 | ||||||
chr12:14917744 | A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.451-441T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917744 | ||||||
chr12:14917862 | C | T | 5 | a0001c0001t0002g0020a0001c0001t0002g0072a0001c0001t0002g0076others(2): Show | 6 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-559G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917862 | ||||||
chr12:14917876 | A | G | 3 | a0001c0001t0003g0129a0001c0001t0003g0244a0001c0001t0003g0245 | 3 | HG01346.hp1 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.451-573T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917876 | ||||||
chr12:14917931 | T | C | 11 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0110others(8): Show | 13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-628A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917931 | ||||||
chr12:14917961 | A | G | 1 | a0002c0002t0002g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.451-658T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14917961 | ||||||
chr12:14918016 | AC | A | 4 | a0001c0001t0001g0062a0001c0001t0008g0012a0001c0001t0008g0111others(1): Show | 6 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-714delG | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918016 | ||||||
chr12:14918020 | A | T | 4 | a0001c0001t0001g0062a0001c0001t0008g0012a0001c0001t0008g0111others(1): Show | 6 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-717T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918020 | ||||||
chr12:14918037 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.451-734A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918037 | ||||||
chr12:14918078 | C | T | 1 | a0001c0001t0003g0221 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.451-775G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918078 | ||||||
chr12:14918086 | G | A | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.451-783C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918086 | ||||||
chr12:14918161 | G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0152 | 3 | NA18952.hp2 NA18962.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.451-858C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918161 | ||||||
chr12:14918308 | G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.451-1005C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918308 | ||||||
chr12:14918336 | C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.451-1033G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918336 | ||||||
chr12:14918520 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.451-1217C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918520 | ||||||
chr12:14918552 | C | G | 1 | a0001c0001t0001g0242 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.451-1249G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918552 | ||||||
chr12:14918569 | CT | C | 30 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(27): Show | 45 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.451-1267delA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918569 | ||||||
chr12:14918678 | A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.451-1375T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918678 | ||||||
chr12:14918713 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.451-1410T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918713 | ||||||
chr12:14918799 | G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.451-1496C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14918799 | ||||||
chr12:14919080 | G | A | 11 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0110others(8): Show | 13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-1777C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919080 | ||||||
chr12:14919118 | C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0274 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.450+1814G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919118 | ||||||
chr12:14919130 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.450+1802T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919130 | ||||||
chr12:14919240 | T | C | 1 | a0001c0001t0002g0086 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.450+1692A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919240 | ||||||
chr12:14919318 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.450+1614A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919318 | ||||||
chr12:14919321 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.450+1611C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919321 | ||||||
chr12:14919420 | A | C | 1 | a0001c0001t0003g0017 | 3 | HG02040.hp1 NA18953.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.450+1512T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919420 | ||||||
chr12:14919475 | C | T | 4 | a0001c0001t0001g0062a0001c0001t0008g0012a0001c0001t0008g0111others(1): Show | 6 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+1457G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919475 | ||||||
chr12:14919476 | A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(285): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.450+1456T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919476 | ||||||
chr12:14919768 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.450+1164G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919768 | ||||||
chr12:14919816 | C | T | 21 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(18): Show | 27 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.450+1116G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919816 | ||||||
chr12:14919948 | C | CA | 18 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0046others(15): Show | 30 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.450+983dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14919948 | ||||||
chr12:14920073 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.450+859C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920073 | ||||||
chr12:14920098 | C | G | 1 | a0002c0002t0004g0124 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.450+834G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920098 | ||||||
chr12:14920145 | C | T | 5 | a0001c0001t0004g0060a0001c0001t0004g0061a0001c0001t0004g0102others(2): Show | 5 | HG00733.hp1 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+787G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920145 | ||||||
chr12:14920198 | T | A | 1 | a0001c0001t0014g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.450+734A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920198 | ||||||
chr12:14920209 | G | C | 5 | a0001c0003t0001g0010a0001c0003t0001g0049a0001c0003t0001g0065others(2): Show | 8 | HG02451.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+723C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920209 | ||||||
chr12:14920307 | C | A | 1 | a0001c0001t0002g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.450+625G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920307 | ||||||
chr12:14920310 | T | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(227): Show | 323 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.450+622A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920310 | ||||||
chr12:14920327 | G | A | 28 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0024others(25): Show | 33 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.450+605C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920327 | ||||||
chr12:14920376 | A | C | 1 | a0001c0001t0003g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.450+556T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920376 | ||||||
chr12:14920695 | C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 295 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.450+237G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920695 | ||||||
chr12:14920711 | C | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 295 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.450+221G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920711 | ||||||
chr12:14920730 | T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 295 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.450+202A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920730 | ||||||
chr12:14920758 | C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(210): Show | 303 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.450+174G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920758 | ||||||
chr12:14920897 | G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 295 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.450+35C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920897 | ||||||
chr12:14920922 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.450+10A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 4/6 | chr12 | 14920922 | ||||||
chr12:14921108 | C | T | 1 | a0001c0003t0001g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-60G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921108 | ||||||
chr12:14921161 | A | G | 1 | a0001c0001t0006g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.334-113T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921161 | ||||||
chr12:14921193 | C | A | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-145G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921193 | ||||||
chr12:14921265 | A | G | 1 | a0001c0001t0005g0279 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.334-217T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921265 | ||||||
chr12:14921379 | A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(163): Show | 245 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.334-331T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921379 | ||||||
chr12:14921396 | A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-348T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921396 | ||||||
chr12:14921442 | G | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-394C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921442 | ||||||
chr12:14921505 | G | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0237 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.334-457C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921505 | ||||||
chr12:14921554 | C | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0126 | 3 | NA18965.hp2 NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.334-506G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921554 | ||||||
chr12:14921636 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.334-588C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921636 | ||||||
chr12:14921723 | G | A | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-675C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921723 | ||||||
chr12:14921748 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.334-700G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921748 | ||||||
chr12:14921828 | C | T | 2 | a0001c0001t0004g0116a0001c0001t0004g0268 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.334-780G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14921828 | ||||||
chr12:14922119 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.334-1071A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922119 | ||||||
chr12:14922144 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.334-1096T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922144 | ||||||
chr12:14922268 | C | T | 56 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0002g0004others(53): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.334-1220G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922268 | ||||||
chr12:14922299 | T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-1251A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922299 | ||||||
chr12:14922482 | T | TTC | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(285): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.334-1436_334-1435d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922482 | ||||||
chr12:14922496 | C | T | 24 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(21): Show | 32 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.334-1448G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922496 | ||||||
chr12:14922641 | G | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0126a0001c0001t0001g0182others(2): Show | 6 | NA18940.hp2 NA18961.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-1593C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922641 | ||||||
chr12:14922716 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.334-1668C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922716 | ||||||
chr12:14922804 | G | A | 8 | a0001c0003t0001g0010a0001c0003t0001g0049a0001c0003t0001g0065others(5): Show | 11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-1756C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922804 | ||||||
chr12:14922842 | G | A | 18 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0033others(15): Show | 22 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.334-1794C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922842 | ||||||
chr12:14922861 | A | T | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-1813T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922861 | ||||||
chr12:14922862 | G | A | 3 | a0001c0001t0005g0115a0001c0001t0005g0279a0001c0001t0006g0063 | 3 | HG01891.hp2 HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.334-1814C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922862 | ||||||
chr12:14922920 | C | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(162): Show | 244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.334-1872G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14922920 | ||||||
chr12:14923009 | G | C | 1 | a0001c0003t0012g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.334-1961C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923009 | ||||||
chr12:14923033 | C | T | 1 | a0001c0001t0004g0271 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.334-1985G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923033 | ||||||
chr12:14923043 | C | T | 1 | a0001c0001t0006g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.334-1995G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923043 | ||||||
chr12:14923067 | C | T | 18 | a0001c0001t0002g0138a0001c0001t0002g0266a0001c0001t0002g0277others(15): Show | 18 | HG00733.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-2019G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923067 | ||||||
chr12:14923068 | T | C | 1 | a0001c0001t0003g0009 | 4 | NA18944.hp2 NA18948.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-2020A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923068 | ||||||
chr12:14923073 | C | CA | 26 | a0001c0001t0002g0019a0001c0001t0002g0023a0001c0001t0002g0077others(23): Show | 33 | HG01123.hp2 HG02015.hp2 HG02083.hp2 others(30): Show |
intron_variant | MODIFIER | c.334-2026dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | ||||||
chr12:14923073 | CA | C | 22 | a0001c0001t0001g0200a0001c0001t0002g0074a0001c0001t0002g0109others(19): Show | 22 | HG00733.hp1 HG01168.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.334-2026delT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | ||||||
chr12:14923073 | CAA | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(164): Show | 250 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.334-2027_334-2026d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | ||||||
chr12:14923073 | CAAA | C | 19 | a0001c0001t0001g0062a0001c0001t0001g0099a0001c0001t0001g0101others(16): Show | 22 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.334-2028_334-2026d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923073 | ||||||
chr12:14923092 | AT | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0170 | 3 | HG00609.hp1 NA18967.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.334-2045delA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923092 | ||||||
chr12:14923396 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.334-2348T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923396 | ||||||
chr12:14923400 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334-2352T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923400 | ||||||
chr12:14923479 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.334-2431A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923479 | ||||||
chr12:14923484 | C | A | 1 | a0001c0001t0002g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2436G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923484 | ||||||
chr12:14923485 | T | A | 1 | a0001c0001t0002g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2437A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923485 | ||||||
chr12:14923486 | A | T | 1 | a0001c0001t0002g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2438T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923486 | ||||||
chr12:14923487 | T | C | 1 | a0001c0001t0002g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-2439A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923487 | ||||||
chr12:14923487 | TAATC | T | 38 | a0001c0001t0001g0053a0001c0001t0001g0140a0001c0001t0001g0153others(35): Show | 44 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.334-2443_334-2440d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923487 | ||||||
chr12:14923488 | A | AATCT | 83 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(80): Show | 123 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.334-2441_334-2440i others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | ||||||
chr12:14923488 | A | AATCTATC others(1): Show |
43 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0031others(40): Show | 55 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.334-2441_334-2440i others(10): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | ||||||
chr12:14923488 | A | AATCTATC others(5): Show |
1 | a0001c0001t0003g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.334-2441_334-2440i others(14): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | ||||||
chr12:14923488 | A | T | 2 | a0001c0001t0002g0266a0001c0001t0002g0277 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.334-2440T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923488 | ||||||
chr12:14923492 | A | AATCT | 21 | a0001c0001t0001g0090a0001c0001t0002g0019a0001c0001t0002g0020others(18): Show | 25 | HG00280.hp1 HG01070.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.334-2448_334-2445d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | ||||||
chr12:14923492 | A | AATCTATC others(1): Show |
17 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0033others(14): Show | 24 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.334-2452_334-2445d others(10): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | ||||||
chr12:14923492 | A | AATCTATC others(5): Show |
1 | a0001c0001t0002g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.334-2456_334-2445d others(14): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | ||||||
chr12:14923492 | A | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(189): Show | 279 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.334-2444T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923492 | ||||||
chr12:14923495 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.334-2447G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923495 | ||||||
chr12:14923496 | T | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0284 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.334-2448A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923496 | ||||||
chr12:14923500 | T | A | 1 | a0001c0001t0002g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.334-2452A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923500 | ||||||
chr12:14923825 | C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-2777G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923825 | ||||||
chr12:14923831 | T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-2783A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14923831 | ||||||
chr12:14924022 | A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 295 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.334-2974T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924022 | ||||||
chr12:14924081 | T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-3033A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924081 | ||||||
chr12:14924088 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.334-3040G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924088 | ||||||
chr12:14924196 | A | G | 12 | a0002c0002t0002g0119a0002c0002t0004g0028a0002c0002t0004g0029others(9): Show | 14 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-3148T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924196 | ||||||
chr12:14924209 | A | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-3161T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924209 | ||||||
chr12:14924210 | C | T | 15 | a0001c0001t0002g0138a0001c0001t0002g0266a0001c0001t0002g0277others(12): Show | 15 | HG00733.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.334-3162G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924210 | ||||||
chr12:14924241 | A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-3193T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924241 | ||||||
chr12:14924286 | C | T | 25 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(22): Show | 33 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.334-3238G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924286 | ||||||
chr12:14924453 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.334-3405T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924453 | ||||||
chr12:14924469 | T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-3421A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924469 | ||||||
chr12:14924555 | T | C | 2 | a0001c0001t0005g0115a0001c0001t0006g0063 | 2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.334-3507A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924555 | ||||||
chr12:14924593 | A | T | 56 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0002g0004others(53): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.334-3545T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924593 | ||||||
chr12:14924625 | G | A | 1 | a0001c0001t0003g0189 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.334-3577C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924625 | ||||||
chr12:14924687 | G | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-3639C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924687 | ||||||
chr12:14924730 | A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-3682T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924730 | ||||||
chr12:14924755 | T | C | 27 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(24): Show | 35 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.334-3707A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924755 | ||||||
chr12:14924917 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.334-3869G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924917 | ||||||
chr12:14924921 | G | A | 3 | a0001c0001t0002g0266a0001c0001t0002g0277a0001c0001t0014g0272 | 3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.334-3873C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14924921 | ||||||
chr12:14925068 | C | G | 8 | a0001c0003t0001g0010a0001c0003t0001g0049a0001c0003t0001g0065others(5): Show | 11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-4020G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925068 | ||||||
chr12:14925109 | C | G | 1 | a0001c0001t0004g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.334-4061G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925109 | ||||||
chr12:14925123 | C | T | 3 | a0001c0001t0008g0012a0001c0001t0008g0111a0001c0001t0008g0267 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-4075G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925123 | ||||||
chr12:14925399 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.334-4351C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925399 | ||||||
chr12:14925538 | C | T | 4 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0274others(1): Show | 4 | HG02735.hp1 HG03669.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-4490G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925538 | ||||||
chr12:14925640 | T | C | 1 | a0001c0001t0003g0239 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-4592A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925640 | ||||||
chr12:14925642 | T | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0277 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.334-4594A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925642 | ||||||
chr12:14925755 | A | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-4707T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925755 | ||||||
chr12:14925759 | C | T | 6 | a0001c0001t0002g0138a0001c0001t0004g0060a0001c0001t0004g0061others(3): Show | 6 | HG00733.hp1 HG01891.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-4711G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925759 | ||||||
chr12:14925795 | C | T | 3 | a0001c0001t0002g0266a0001c0001t0002g0277a0001c0001t0014g0272 | 3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.334-4747G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925795 | ||||||
chr12:14925796 | G | A | 2 | a0001c0001t0001g0173a0001c0001t0007g0174 | 2 | NA18942.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.334-4748C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925796 | ||||||
chr12:14925826 | T | A | 11 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0110others(8): Show | 13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.334-4778A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925826 | ||||||
chr12:14925842 | G | C | 8 | a0001c0003t0001g0010a0001c0003t0001g0049a0001c0003t0001g0065others(5): Show | 11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-4794C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925842 | ||||||
chr12:14925848 | C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-4800G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925848 | ||||||
chr12:14925946 | G | A | 11 | a0002c0002t0004g0028a0002c0002t0004g0029a0002c0002t0004g0110others(8): Show | 13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.334-4898C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14925946 | ||||||
chr12:14926069 | C | CA | 19 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0033others(16): Show | 23 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.334-5022dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926069 | ||||||
chr12:14926256 | C | A | 1 | a0001c0001t0003g0245 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.334-5208G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926256 | ||||||
chr12:14926281 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.334-5233A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926281 | ||||||
chr12:14926285 | GTATTAA | G | 3 | a0001c0001t0002g0266a0001c0001t0002g0277a0001c0001t0014g0272 | 3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.334-5243_334-5238d others(8): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926285 | ||||||
chr12:14926428 | T | C | 1 | a0001c0001t0002g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.334-5380A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926428 | ||||||
chr12:14926436 | A | G | 1 | a0001c0001t0003g0043 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.334-5388T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926436 | ||||||
chr12:14926447 | C | T | 2 | a0001c0001t0011g0030a0001c0001t0011g0125 | 3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.334-5399G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926447 | ||||||
chr12:14926486 | A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(229): Show | 325 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.334-5438T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926486 | ||||||
chr12:14926517 | C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(189): Show | 279 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.334-5469G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926517 | ||||||
chr12:14926662 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.334-5614T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926662 | ||||||
chr12:14926693 | A | T | 1 | a0001c0001t0004g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-5645T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926693 | ||||||
chr12:14926748 | G | A | 2 | a0001c0001t0011g0030a0001c0001t0011g0125 | 3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.334-5700C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926748 | ||||||
chr12:14926977 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.334-5929G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926977 | ||||||
chr12:14926979 | G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0159a0001c0001t0001g0165others(1): Show | 6 | HG00735.hp1 HG01255.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-5931C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14926979 | ||||||
chr12:14927024 | C | T | 1 | a0001c0001t0005g0279 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.334-5976G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927024 | ||||||
chr12:14927052 | G | A | 1 | a0002c0002t0004g0120 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.334-6004C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927052 | ||||||
chr12:14927073 | G | A | 3 | a0001c0001t0008g0012a0001c0001t0008g0111a0001c0001t0008g0267 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6025C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927073 | ||||||
chr12:14927101 | C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(162): Show | 244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.334-6053G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927101 | ||||||
chr12:14927324 | C | T | 8 | a0001c0003t0001g0010a0001c0003t0001g0049a0001c0003t0001g0065others(5): Show | 11 | HG02145.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-6276G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927324 | ||||||
chr12:14927333 | A | ATG | 2 | a0001c0003t0012g0022a0001c0003t0012g0113 | 3 | HG02258.hp1 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.334-6287_334-6286d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927333 | ||||||
chr12:14927347 | G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0046others(24): Show | 41 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.334-6299C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927347 | ||||||
chr12:14927349 | A | G | 57 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0002g0004others(54): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-6301T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927349 | ||||||
chr12:14927351 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.334-6303T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927351 | ||||||
chr12:14927425 | T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-6377A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927425 | ||||||
chr12:14927499 | GTGT | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(188): Show | 278 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.334-6454_334-6452d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927499 | ||||||
chr12:14927584 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.334-6536G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927584 | ||||||
chr12:14927596 | T | G | 1 | a0001c0001t0003g0191 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.334-6548A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927596 | ||||||
chr12:14927712 | TC | T | 56 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0002g0004others(53): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.334-6665delG | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927712 | ||||||
chr12:14927714 | C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.334-6666G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927714 | ||||||
chr12:14927744 | G | GCACA | 4 | a0002c0002t0004g0110a0002c0002t0004g0121a0002c0002t0004g0123others(1): Show | 4 | HG02165.hp1 NA18978.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-6700_334-6697d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | ||||||
chr12:14927744 | G | GCACACA | 4 | a0002c0002t0002g0119a0002c0002t0004g0028a0002c0002t0004g0029others(1): Show | 6 | HG02083.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-6702_334-6697d others(8): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | ||||||
chr12:14927744 | G | GCACACAC others(3): Show |
2 | a0002c0002t0004g0118a0002c0002t0004g0122 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.334-6706_334-6697d others(12): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | ||||||
chr12:14927744 | GCA | G | 59 | a0001c0001t0001g0100a0001c0001t0001g0130a0001c0001t0001g0232others(56): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.334-6698_334-6697d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | ||||||
chr12:14927744 | GCACA | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 284 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.334-6700_334-6697d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | ||||||
chr12:14927744 | GCACACA | G | 12 | a0001c0001t0001g0066a0001c0001t0001g0140a0001c0001t0001g0168others(9): Show | 12 | HG02145.hp2 HG02155.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-6702_334-6697d others(8): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14927744 | ||||||
chr12:14928084 | A | G | 1 | a0001c0001t0003g0202 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.333+6772T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928084 | ||||||
chr12:14928107 | C | A | 1 | a0001c0001t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.333+6749G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928107 | ||||||
chr12:14928272 | G | C | 1 | a0001c0001t0003g0234 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.333+6584C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928272 | ||||||
chr12:14928284 | G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.333+6572C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928284 | ||||||
chr12:14928286 | G | A | 1 | a0001c0001t0005g0235 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.333+6570C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928286 | ||||||
chr12:14928355 | G | A | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+6501C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928355 | ||||||
chr12:14928400 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.333+6456A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928400 | ||||||
chr12:14928512 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.333+6344A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928512 | ||||||
chr12:14928540 | G | A | 1 | a0001c0003t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.333+6316C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928540 | ||||||
chr12:14928559 | A | G | 4 | a0001c0001t0001g0062a0001c0001t0004g0128a0001c0001t0004g0135others(1): Show | 4 | HG01934.hp1 HG02055.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+6297T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928559 | ||||||
chr12:14928599 | C | G | 1 | a0001c0001t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.333+6257G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928599 | ||||||
chr12:14928700 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.333+6156T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928700 | ||||||
chr12:14928712 | C | T | 1 | a0001c0001t0015g0259 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.333+6144G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928712 | ||||||
chr12:14928844 | C | T | 3 | a0001c0001t0005g0115a0001c0001t0005g0279a0001c0001t0006g0063 | 3 | HG01891.hp2 HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.333+6012G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928844 | ||||||
chr12:14928936 | G | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19006.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.333+5920C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928936 | ||||||
chr12:14928963 | A | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(285): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.333+5893T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928963 | ||||||
chr12:14928964 | G | A | 63 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0001g0181others(60): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.333+5892C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14928964 | ||||||
chr12:14929056 | A | G | 3 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0183 | 5 | HG00423.hp2 HG00621.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+5800T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929056 | ||||||
chr12:14929070 | T | A | 63 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0001g0181others(60): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.333+5786A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929070 | ||||||
chr12:14929140 | C | G | 1 | a0002c0002t0004g0028 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.333+5716G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929140 | ||||||
chr12:14929143 | C | G | 6 | a0001c0001t0002g0176a0001c0003t0001g0010a0001c0003t0001g0049others(3): Show | 9 | HG02451.hp2 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+5713G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929143 | ||||||
chr12:14929162 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.333+5694G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929162 | ||||||
chr12:14929163 | G | A | 2 | a0001c0003t0001g0010a0001c0003t0001g0065 | 4 | HG02451.hp2 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+5693C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929163 | ||||||
chr12:14929191 | G | A | 1 | a0001c0001t0009g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.333+5665C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929191 | ||||||
chr12:14929311 | G | C | 1 | a0001c0001t0003g0239 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.333+5545C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929311 | ||||||
chr12:14929346 | T | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 13 | HG01257.hp2 HG01258.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+5510A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929346 | ||||||
chr12:14929363 | C | T | 1 | a0001c0001t0004g0271 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.333+5493G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929363 | ||||||
chr12:14929448 | T | C | 38 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(35): Show | 44 | HG00733.hp1 HG01109.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.333+5408A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929448 | ||||||
chr12:14929484 | G | A | 1 | a0001c0001t0004g0116 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.333+5372C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929484 | ||||||
chr12:14929508 | A | G | 3 | a0001c0001t0002g0266a0001c0001t0002g0277a0001c0001t0014g0272 | 3 | HG02451.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.333+5348T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929508 | ||||||
chr12:14929566 | T | C | 3 | a0001c0001t0008g0012a0001c0001t0008g0111a0001c0001t0008g0267 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5290A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929566 | ||||||
chr12:14929742 | A | C | 2 | a0001c0001t0006g0137a0001c0001t0006g0161 | 2 | HG02004.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.333+5114T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929742 | ||||||
chr12:14929861 | G | T | 3 | a0001c0001t0008g0012a0001c0001t0008g0111a0001c0001t0008g0267 | 5 | HG02055.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4995C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929861 | ||||||
chr12:14929903 | G | T | 2 | a0001c0001t0007g0015a0001c0001t0007g0197 | 4 | NA18955.hp1 NA19064.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+4953C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929903 | ||||||
chr12:14929919 | G | C | 1 | a0002c0002t0002g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.333+4937C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14929919 | ||||||
chr12:14930082 | A | G | 1 | a0001c0001t0003g0009 | 4 | NA18944.hp2 NA18948.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+4774T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930082 | ||||||
chr12:14930098 | G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0097a0001c0001t0002g0098 | 5 | HG00558.hp1 HG02071.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+4758C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930098 | ||||||
chr12:14930140 | C | A | 1 | a0001c0001t0004g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.333+4716G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930140 | ||||||
chr12:14930150 | A | C | 110 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(107): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.333+4706T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930150 | ||||||
chr12:14930214 | G | A | 1 | a0001c0001t0006g0161 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.333+4642C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930214 | ||||||
chr12:14930268 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.333+4588C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930268 | ||||||
chr12:14930268 | G | C | 3 | a0001c0001t0005g0115a0001c0001t0005g0279a0001c0001t0006g0063 | 3 | HG01891.hp2 HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.333+4588C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930268 | ||||||
chr12:14930297 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.333+4559T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930297 | ||||||
chr12:14930485 | G | C | 3 | a0001c0001t0003g0129a0001c0001t0003g0244a0001c0001t0003g0245 | 3 | HG01346.hp1 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.333+4371C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930485 | ||||||
chr12:14930529 | A | G | 24 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(21): Show | 30 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.333+4327T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930529 | ||||||
chr12:14930576 | A | T | 85 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0099others(82): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.333+4280T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930576 | ||||||
chr12:14930588 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.333+4268G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930588 | ||||||
chr12:14930619 | T | C | 1 | a0001c0001t0014g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.333+4237A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930619 | ||||||
chr12:14930626 | C | CTTA | 85 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0099others(82): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.333+4227_333+4229d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930626 | ||||||
chr12:14930651 | A | C | 24 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(21): Show | 30 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.333+4205T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930651 | ||||||
chr12:14930788 | C | T | 3 | a0001c0001t0014g0272a0001c0003t0001g0010a0001c0003t0001g0065 | 5 | HG02451.hp2 HG02970.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4068G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930788 | ||||||
chr12:14930933 | A | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(285): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.333+3923T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930933 | ||||||
chr12:14930963 | T | C | 11 | a0002c0002t0002g0119a0002c0002t0004g0028a0002c0002t0004g0029others(8): Show | 13 | HG02015.hp2 HG02083.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+3893A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14930963 | ||||||
chr12:14931045 | C | G | 1 | a0001c0001t0002g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333+3811G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931045 | ||||||
chr12:14931088 | G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0082a0001c0001t0001g0247 | 5 | HG01175.hp1 HG01433.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+3768C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931088 | ||||||
chr12:14931158 | ATTTC | A | 26 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0001g0181others(23): Show | 41 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.333+3694_333+3697d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931158 | ||||||
chr12:14931177 | A | G | 85 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0067others(82): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.333+3679T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931177 | ||||||
chr12:14931308 | A | G | 2 | a0001c0001t0011g0030a0001c0001t0011g0125 | 3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.333+3548T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931308 | ||||||
chr12:14931363 | C | A | 1 | a0001c0001t0001g0192 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.333+3493G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | ||||||
chr12:14931363 | C | CA | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(161): Show | 248 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.333+3492dupT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | ||||||
chr12:14931363 | C | CAA | 24 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0050others(21): Show | 29 | HG01109.hp1 HG02027.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.333+3491_333+3492d others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | ||||||
chr12:14931363 | CA | C | 58 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0067others(55): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.333+3492delT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931363 | ||||||
chr12:14931747 | G | A | 1 | a0003c0004t0010g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.333+3109C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931747 | ||||||
chr12:14931773 | G | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0276a0001c0001t0001g0281others(3): Show | 7 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+3083C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931773 | ||||||
chr12:14931833 | G | A | 2 | a0001c0001t0006g0162a0001c0001t0006g0163 | 2 | HG01081.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.333+3023C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931833 | ||||||
chr12:14931867 | AATT | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0112a0001c0001t0001g0114others(2): Show | 7 | HG02258.hp1 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+2986_333+2988d others(5): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931867 | ||||||
chr12:14931906 | CA | C | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+2949delT | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931906 | ||||||
chr12:14931958 | C | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0112a0001c0001t0001g0114others(5): Show | 10 | HG02258.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+2898G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14931958 | ||||||
chr12:14932056 | A | C | 2 | a0001c0001t0005g0115a0001c0003t0001g0270 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.333+2800T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932056 | ||||||
chr12:14932266 | A | T | 9 | a0001c0001t0001g0054a0001c0001t0001g0276a0001c0001t0001g0278others(6): Show | 10 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+2590T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932266 | ||||||
chr12:14932331 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.333+2525C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932331 | ||||||
chr12:14932349 | T | C | 1 | a0001c0001t0002g0106 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.333+2507A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932349 | ||||||
chr12:14932385 | C | T | 4 | a0001c0001t0001g0273a0001c0001t0014g0272a0001c0003t0001g0010others(1): Show | 6 | HG02451.hp2 HG02897.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+2471G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932385 | ||||||
chr12:14932422 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.333+2434A>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932422 | ||||||
chr12:14932680 | C | T | 62 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(59): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.333+2176G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932680 | ||||||
chr12:14932717 | T | C | 1 | a0002c0002t0004g0123 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.333+2139A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932717 | ||||||
chr12:14932871 | T | C | 1 | a0001c0001t0003g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.333+1985A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932871 | ||||||
chr12:14932942 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.333+1914G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14932942 | ||||||
chr12:14933016 | T | C | 87 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0062others(84): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.333+1840A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933016 | ||||||
chr12:14933020 | G | A | 1 | a0001c0001t0015g0259 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.333+1836C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933020 | ||||||
chr12:14933073 | T | TATTC | 6 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0003t0012g0113others(3): Show | 7 | HG02145.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+1779_333+1782d others(6): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933073 | ||||||
chr12:14933101 | G | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0114a0001c0003t0012g0113 | 4 | HG02486.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+1755C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933101 | ||||||
chr12:14933366 | G | A | 2 | a0001c0001t0003g0051a0001c0001t0003g0052 | 4 | NA18953.hp2 NA18973.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+1490C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933366 | ||||||
chr12:14933506 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.333+1350A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933506 | ||||||
chr12:14933509 | T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.333+1347A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933509 | ||||||
chr12:14933560 | A | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 9 | HG00609.hp1 NA18940.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+1296T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933560 | ||||||
chr12:14933652 | A | C | 1 | a0001c0001t0004g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.333+1204T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933652 | ||||||
chr12:14933984 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.333+872G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14933984 | ||||||
chr12:14934083 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.333+773G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934083 | ||||||
chr12:14934089 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.333+767A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934089 | ||||||
chr12:14934115 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.333+741T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934115 | ||||||
chr12:14934192 | G | T | 1 | a0001c0001t0002g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.333+664C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934192 | ||||||
chr12:14934281 | T | C | 84 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0064others(81): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.333+575A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934281 | ||||||
chr12:14934339 | A | G | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 26 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.333+517T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934339 | ||||||
chr12:14934422 | G | A | 2 | a0001c0001t0004g0271a0001c0003t0001g0270 | 2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.333+434C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934422 | ||||||
chr12:14934441 | A | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0131a0001c0001t0001g0133others(2): Show | 6 | HG00621.hp1 HG02027.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+415T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934441 | ||||||
chr12:14934518 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.333+338T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934518 | ||||||
chr12:14934558 | A | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 5 | HG02132.hp1 HG02155.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+298T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934558 | ||||||
chr12:14934622 | G | A | 1 | a0002c0002t0004g0124 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.333+234C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934622 | ||||||
chr12:14934719 | A | G | 1 | a0001c0001t0004g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.333+137T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934719 | ||||||
chr12:14934838 | G | C | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG02976.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.333+18C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 3/6 | chr12 | 14934838 | ||||||
chr12:14935018 | C | T | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.196-25G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935018 | ||||||
chr12:14935040 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196-47G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935040 | ||||||
chr12:14935112 | G | GTAAC | 2 | a0001c0001t0002g0024a0001c0001t0002g0107 | 3 | HG02622.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-123_196-120dup others(4): Show |
ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935112 | ||||||
chr12:14935181 | G | C | 2 | a0001c0001t0001g0273a0001c0001t0014g0272 | 2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.196-188C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935181 | ||||||
chr12:14935201 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196-208C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935201 | ||||||
chr12:14935225 | C | A | 1 | a0001c0001t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196-232G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935225 | ||||||
chr12:14935263 | G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0112a0001c0001t0001g0114others(1): Show | 5 | HG02486.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-270C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935263 | ||||||
chr12:14935351 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.196-358T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935351 | ||||||
chr12:14935531 | A | T | 2 | a0001c0001t0008g0012a0001c0001t0008g0111 | 4 | HG02280.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-538T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935531 | ||||||
chr12:14935715 | T | C | 1 | a0001c0001t0004g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.196-722A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935715 | ||||||
chr12:14935717 | G | A | 65 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(62): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.196-724C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935717 | ||||||
chr12:14935885 | A | C | 21 | a0001c0001t0001g0027a0001c0001t0001g0273a0001c0001t0004g0116others(18): Show | 27 | HG00733.hp1 HG02015.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.196-892T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935885 | ||||||
chr12:14935895 | T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG00323.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196-902A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935895 | ||||||
chr12:14935977 | C | T | 46 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0032others(43): Show | 56 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.196-984G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14935977 | ||||||
chr12:14936007 | T | C | 84 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0064others(81): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.196-1014A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936007 | ||||||
chr12:14936008 | C | A | 1 | a0001c0001t0002g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196-1015G>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936008 | ||||||
chr12:14936018 | G | A | 3 | a0001c0001t0002g0025a0001c0001t0002g0109a0002c0002t0004g0110 | 4 | NA19055.hp2 NA19062.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-1025C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936018 | ||||||
chr12:14936098 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196-1105G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936098 | ||||||
chr12:14936295 | A | G | 2 | a0001c0001t0001g0273a0001c0001t0014g0272 | 2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.196-1302T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936295 | ||||||
chr12:14936331 | G | A | 2 | a0001c0001t0008g0012a0001c0001t0008g0111 | 4 | HG02280.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1338C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936331 | ||||||
chr12:14936349 | C | G | 1 | a0001c0001t0014g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196-1356G>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936349 | ||||||
chr12:14936411 | G | C | 4 | a0001c0001t0001g0269a0001c0001t0002g0266a0001c0001t0004g0268others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-1418C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936411 | ||||||
chr12:14936482 | A | C | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1470T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936482 | ||||||
chr12:14936503 | C | T | 2 | a0001c0001t0001g0273a0001c0001t0014g0272 | 2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.195+1449G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936503 | ||||||
chr12:14936570 | T | C | 2 | a0001c0001t0001g0273a0001c0001t0014g0272 | 2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.195+1382A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936570 | ||||||
chr12:14936605 | A | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0112a0001c0001t0001g0114others(1): Show | 5 | HG02486.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+1347T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936605 | ||||||
chr12:14936621 | G | C | 1 | a0001c0001t0001g0053 | 2 | NA18940.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.195+1331C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936621 | ||||||
chr12:14936623 | T | C | 2 | a0001c0001t0011g0030a0001c0001t0011g0125 | 3 | HG02135.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.195+1329A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936623 | ||||||
chr12:14936646 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.195+1306T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936646 | ||||||
chr12:14936726 | A | G | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1226T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936726 | ||||||
chr12:14936824 | C | T | 2 | a0001c0001t0004g0127a0001c0001t0004g0128 | 2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.195+1128G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936824 | ||||||
chr12:14936869 | G | T | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1083C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936869 | ||||||
chr12:14936890 | A | G | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+1062T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936890 | ||||||
chr12:14936975 | A | G | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+977T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14936975 | ||||||
chr12:14937047 | C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0006g0063 | 3 | HG01934.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195+905G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937047 | ||||||
chr12:14937080 | C | T | 2 | a0001c0001t0004g0060a0001c0001t0004g0061 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.195+872G>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937080 | ||||||
chr12:14937156 | T | A | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+796A>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937156 | ||||||
chr12:14937412 | A | G | 65 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(62): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.195+540T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937412 | ||||||
chr12:14937421 | A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0126 | 3 | NA18965.hp2 NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.195+531T>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937421 | ||||||
chr12:14937438 | A | C | 88 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0062others(85): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.195+514T>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937438 | ||||||
chr12:14937460 | G | A | 3 | a0003c0004t0010g0056a0003c0004t0010g0057a0003c0004t0010g0058 | 3 | HG02145.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.195+492C>T | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937460 | ||||||
chr12:14937658 | A | G | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+294T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937658 | ||||||
chr12:14937828 | G | C | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+124C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937828 | ||||||
chr12:14937835 | G | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.195+117C>A | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937835 | ||||||
chr12:14937903 | A | G | 67 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(64): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.195+49T>C | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 2/6 | chr12 | 14937903 | ||||||
chr12:14938073 | T | C | 2 | a0001c0001t0004g0271a0001c0003t0001g0270 | 2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.95-21A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938073 | ||||||
chr12:14938120 | T | C | 2 | a0001c0001t0001g0273a0001c0001t0014g0272 | 2 | HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.95-68A>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938120 | ||||||
chr12:14938217 | G | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG00735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.95-165C>G | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938217 | ||||||
chr12:14938287 | A | AT | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(270): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.94+127_94+128insA | ERP27 | ENSG00000139055.7 | transcript | ENST00000266397.7 | protein_coding | 1/6 | chr12 | 14938287 |