geneid | 9166 |
---|---|
ensemblid | ENSG00000147654.16 |
hgncid | 3123 |
symbol | EBAG9 |
name | estrogen receptor binding site associated antigen 9 |
refseq_nuc | NM_004215.5 |
refseq_prot | NP_004206.1 |
ensembl_nuc | ENST00000337573.10 |
ensembl_prot | ENSP00000337675.5 |
mane_status | MANE Select |
chr | chr8 |
start | 109540173 |
end | 109565996 |
strand | + |
ver | v1.2 |
region | chr8:109540173-109565996 |
region5000 | chr8:109535173-109570996 |
regionname0 | EBAG9_chr8_109540173_109565996 |
regionname5000 | EBAG9_chr8_109535173_109570996 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 213 | 356 | 96 | 74 | 132 | 16 | 36 | 98 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 642 | 356 | 96 | 74 | 132 | 16 | 36 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1742 | 139 | 19 | 30 | 71 | 6 | 12 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0002 | 0/0 | 1742 | 90 | 56 | 19 | 0 | 3 | 12 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0003 | 1/0 | 1742 | 89 | 2 | 20 | 53 | 6 | 7 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0004 | 0/0 | 1739 | 6 | 6 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0005 | 0/0 | 1742 | 4 | 4 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0006 | 0/0 | 1742 | 3 | 0 | 1 | 0 | 1 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0007 | 0/0 | 1742 | 3 | 0 | 1 | 0 | 0 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0008 | 0/0 | 1742 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0009 | 0/0 | 1740 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0010 | 0/0 | 1742 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0011 | 0/0 | 1742 | 2 | 0 | 0 | 0 | 0 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0012 | 0/0 | 1742 | 2 | 0 | 2 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0013 | 0/0 | 1742 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0014 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0015 | 0/0 | 1739 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0016 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0017 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0018 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0019 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0020 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0021 | 0/0 | 1742 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
t0022 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 31 | 0 | 8 | 18 | 1 | 4 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0002 | 0/0 | 11 | 0 | 0 | 7 | 0 | 4 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0003 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0004 | 0/0 | 8 | 3 | 3 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0005 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0006 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0007 | 0/0 | 6 | 0 | 3 | 0 | 1 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0008 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0023 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0024 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0026 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0030 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0038 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 642 | 356 | 96 | 74 | 132 | 16 | 36 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2383 | 139 | 19 | 30 | 71 | 6 | 12 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0002 | 0/0 | 2383 | 90 | 56 | 19 | 0 | 3 | 12 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0003 | 1/0 | 2383 | 89 | 2 | 20 | 53 | 6 | 7 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0004 | 0/0 | 2380 | 6 | 6 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0005 | 0/0 | 2383 | 4 | 4 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0006 | 0/0 | 2383 | 3 | 0 | 1 | 0 | 1 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0007 | 0/0 | 2383 | 3 | 0 | 1 | 0 | 0 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0008 | 0/0 | 2383 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0009 | 0/0 | 2381 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0010 | 0/0 | 2383 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0011 | 0/0 | 2383 | 2 | 0 | 0 | 0 | 0 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0012 | 0/0 | 2383 | 2 | 0 | 2 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0013 | 0/0 | 2383 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0014 | 0/0 | 2381 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0015 | 0/0 | 2380 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0016 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0017 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0018 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0019 | 0/0 | 2383 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0020 | 0/0 | 2383 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0021 | 0/0 | 2383 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
a0001c0001t0022 | 0/0 | 2383 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | copy fasta | chr8 | 109535173 | 109570996 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 23 | 0 | 6 | 16 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0004 | 0/0 | 7 | 3 | 3 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 3 | 0 | 1 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0030 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0006 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0008 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0002 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0005 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0024 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0026 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0004g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0006g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0007g0001 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0009g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0010g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0011g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0013g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0015g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0016g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0017g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0018g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0019g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0021g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
a0001c0001t0022g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | GBR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0147 | EUR | GBR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | GBR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0026 | EUR | FIN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00558 | hp2 | a0001 | c0001 | t0017 | g0108 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00621 | hp1 | a0001 | c0001 | t0010 | g0088 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01069 | hp1 | a0001 | c0001 | t0012 | g0153 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01071 | hp2 | a0001 | c0001 | t0012 | g0005 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01106 | hp1 | a0001 | c0001 | t0021 | g0009 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0012 | EUR | IBS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0059 | EUR | IBS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | IBS | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02080 | hp2 | a0001 | c0001 | t0010 | g0131 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02145 | hp1 | a0001 | c0001 | t0019 | g0179 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02257 | hp1 | a0001 | c0001 | t0014 | g0145 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02602 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0054 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0029 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03239 | hp1 | a0001 | c0001 | t0011 | g0002 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03486 | hp2 | a0001 | c0001 | t0022 | g0198 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03490 | hp2 | a0001 | c0001 | t0011 | g0002 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03579 | hp1 | a0001 | c0001 | t0013 | g0023 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03704 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | STU | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | YRI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | CHB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | YRI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | YRI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18977 | hp2 | a0001 | c0001 | t0016 | g0085 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18990 | hp1 | a0001 | c0001 | t0018 | g0004 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19011 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | LWK | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19056 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19072 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19089 | hp1 | a0001 | c0001 | t0008 | g0119 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | YRI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0023 | AFR | YRI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ASW | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0148 | EUR | TSI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0001 | EUR | TSI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | TSI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0001 | SAS | GIH | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | USA | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | USA | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | USA | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0115 | REF | REF | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0111 | REF | REF | EBAG9_chr8_109535173_109570996 | EBAG9 | chr8 | 109535173 | 109570996 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:109540214
|
C | G | 1 | a0001c0001t0022 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-263C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/7 | 10611 | chr8 | 109540214 | |||||
chr8:109540230
|
C | T | 1 | a0001c0001t0013 | 2 | HG03579.hp1 NA19240.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-247C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/7 | chr8 | 109540230 | ||||||
chr8:109540348
|
T | C | 17 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
5_prime_UTR_variant | MODIFIER | c.-129T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/7 | 10477 | chr8 | 109540348 | |||||
chr8:109540355
|
A | G | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-122A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/7 | 10470 | chr8 | 109540355 | |||||
chr8:109540452
|
T | C | 2 | a0001c0001t0006a0001c0001t0007 | 6 | HG01123.hp2 HG01257.hp2 HG02602.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-25T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/7 | 10373 | chr8 | 109540452 | |||||
chr8:109564755
|
CTT | C | 2 | a0001c0001t0009a0001c0001t0014 | 3 | HG02257.hp1 HG02280.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*197_*198delTT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 197 | chr8 | 109564755 | |||||
chr8:109564790
|
T | C | 1 | a0001c0001t0015 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 231 | chr8 | 109564790 | |||||
chr8:109564846
|
C | T | 1 | a0001c0001t0012 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*287C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 287 | chr8 | 109564846 | |||||
chr8:109564930
|
A | T | 1 | a0001c0001t0011 | 2 | HG03239.hp1 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*371A>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 371 | chr8 | 109564930 | |||||
chr8:109565009
|
G | A | 1 | a0001c0001t0005 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*450G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 450 | chr8 | 109565009 | |||||
chr8:109565170
|
G | A | 1 | a0001c0001t0008 | 3 | NA19011.hp1 NA19056.hp2 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*611G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 611 | chr8 | 109565170 | |||||
chr8:109565172
|
ACAT | A | 2 | a0001c0001t0004a0001c0001t0015 | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*617_*619delCAT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 617 | INFO_REALIGN_3_PRIME | chr8 | 109565172 | ||||
chr8:109565174
|
A | G | 1 | a0001c0001t0019 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*615A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 615 | chr8 | 109565174 | |||||
chr8:109565177
|
A | G | 1 | a0001c0001t0007 | 3 | HG01123.hp2 HG02602.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*618A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 618 | chr8 | 109565177 | |||||
chr8:109565290
|
A | G | 1 | a0001c0001t0010 | 2 | HG00621.hp1 HG02080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*731A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 731 | chr8 | 109565290 | |||||
chr8:109565319
|
A | G | 1 | a0001c0001t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 760 | chr8 | 109565319 | |||||
chr8:109565463
|
G | A | 1 | a0001c0001t0016 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 904 | chr8 | 109565463 | |||||
chr8:109565526
|
G | A | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(6): Show | 107 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*967G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 967 | chr8 | 109565526 | |||||
chr8:109565737
|
C | T | 1 | a0001c0001t0009 | 2 | HG02280.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1178C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 1178 | chr8 | 109565737 | |||||
chr8:109565823
|
A | G | 1 | a0001c0001t0018 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 1264 | chr8 | 109565823 | |||||
chr8:109565835
|
A | G | 1 | a0001c0001t0017 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1276A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 7/7 | 1276 | chr8 | 109565835 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:109540473
|
T | G | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+12T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109540473 | ||||||
chr8:109540531
|
TCTTTC | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 6 | HG01934.hp2 HG02132.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+75_-16+79delCC others(3): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109540531 | |||||
chr8:109540579
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-16+118C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109540579 | ||||||
chr8:109540635
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-16+174A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109540635 | ||||||
chr8:109540749
|
T | C | 1 | a0001c0001t0020g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+288T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109540749 | ||||||
chr8:109540990
|
GAA | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0203 | 3 | HG02615.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-16+532_-16+533del others(2): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109540990 | |||||
chr8:109541049
|
A | AT | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+596dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109541049 | |||||
chr8:109541279
|
AAGATACT others(1): Show |
A | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+820_-16+827del others(8): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109541279 | |||||
chr8:109541315
|
C | T | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+854C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541315 | ||||||
chr8:109541365
|
G | A | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+904G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541365 | ||||||
chr8:109541533
|
C | T | 16 | a0001c0001t0002g0015a0001c0001t0002g0048a0001c0001t0002g0180others(13): Show | 20 | HG00741.hp2 HG02615.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-16+1072C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541533 | ||||||
chr8:109541542
|
A | G | 1 | a0001c0001t0019g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+1081A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541542 | ||||||
chr8:109541614
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-16+1153A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541614 | ||||||
chr8:109541880
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-16+1419T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541880 | ||||||
chr8:109541988
|
C | A | 1 | a0001c0001t0002g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-16+1527C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541988 | ||||||
chr8:109541996
|
G | T | 1 | a0001c0001t0003g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-16+1535G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541996 | ||||||
chr8:109541997
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-16+1536T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109541997 | ||||||
chr8:109542000
|
T | A | 1 | a0001c0001t0003g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-16+1539T>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542000 | ||||||
chr8:109542088
|
T | C | 1 | a0001c0001t0003g0076 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-16+1627T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542088 | ||||||
chr8:109542141
|
A | G | 1 | a0001c0001t0019g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+1680A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542141 | ||||||
chr8:109542239
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-16+1778A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542239 | ||||||
chr8:109542480
|
A | G | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | NA18999.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-16+2019A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542480 | ||||||
chr8:109542602
|
T | C | 1 | a0001c0001t0020g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+2141T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542602 | ||||||
chr8:109542660
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-16+2199A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542660 | ||||||
chr8:109542759
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-16+2298A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542759 | ||||||
chr8:109542836
|
C | G | 1 | a0001c0001t0003g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-16+2375C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109542836 | ||||||
chr8:109543097
|
A | G | 1 | a0001c0001t0001g0047 | 2 | HG00597.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-16+2636A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543097 | ||||||
chr8:109543117
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-16+2656A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543117 | ||||||
chr8:109543135
|
C | CT | 30 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 41 | HG00423.hp1 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-16+2705dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
C | CTT | 25 | a0001c0001t0001g0025a0001c0001t0001g0146a0001c0001t0001g0172others(22): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.-16+2704_-16+2705d others(4): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
C | CTTT | 23 | a0001c0001t0001g0156a0001c0001t0002g0008a0001c0001t0002g0016others(20): Show | 37 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.-16+2703_-16+2705d others(5): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
C | CTTTT | 15 | a0001c0001t0002g0006a0001c0001t0002g0065a0001c0001t0002g0066others(12): Show | 29 | HG00735.hp1 HG00741.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+2702_-16+2705d others(6): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
C | CTTTTT | 9 | a0001c0001t0001g0170a0001c0001t0002g0072a0001c0001t0002g0073others(6): Show | 10 | HG00423.hp2 HG00639.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+2701_-16+2705d others(7): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0005g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-16+2695_-16+2705d others(13): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0005g0031a0001c0001t0005g0053 | 3 | HG02572.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-16+2694_-16+2705d others(14): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0002g0083a0001c0001t0002g0084 | 2 | HG00733.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-16+2691_-16+2705d others(17): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543135
|
CTTTTTTT others(9): Show |
C | 36 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0018others(33): Show | 51 | HG00741.hp2 HG01074.hp1 HG01261.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16+2690_-16+2705d others(18): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109543135 | |||||
chr8:109543357
|
G | T | 5 | a0001c0001t0002g0048a0001c0001t0002g0190a0001c0001t0002g0191others(2): Show | 6 | HG00741.hp2 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+2896G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543357 | ||||||
chr8:109543509
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16+3048T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543509 | ||||||
chr8:109543541
|
A | C | 1 | a0001c0001t0003g0155 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-16+3080A>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543541 | ||||||
chr8:109543563
|
A | C | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+3102A>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543563 | ||||||
chr8:109543573
|
T | C | 3 | a0001c0001t0002g0006a0001c0001t0002g0065a0001c0001t0002g0072 | 8 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+3112T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543573 | ||||||
chr8:109543692
|
T | C | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+3231T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543692 | ||||||
chr8:109543758
|
T | C | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+3297T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543758 | ||||||
chr8:109543799
|
G | A | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+3338G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543799 | ||||||
chr8:109543799
|
G | T | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+3338G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543799 | ||||||
chr8:109543828
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-16+3367C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543828 | ||||||
chr8:109543937
|
C | T | 11 | a0001c0001t0002g0015a0001c0001t0002g0180a0001c0001t0002g0181others(8): Show | 14 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16+3476C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543937 | ||||||
chr8:109543945
|
A | G | 137 | a0001c0001t0001g0030a0001c0001t0001g0126a0001c0001t0001g0170others(134): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-16+3484A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109543945 | ||||||
chr8:109544033
|
TA | T | 99 | a0001c0001t0001g0030a0001c0001t0001g0116a0001c0001t0001g0117others(96): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-16+3592delA | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109544033 | |||||
chr8:109544033
|
TAA | T | 21 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0033others(18): Show | 29 | HG00733.hp2 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-16+3591_-16+3592d others(4): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109544033 | |||||
chr8:109544033
|
TAAA | T | 6 | a0001c0001t0002g0082a0001c0001t0004g0029a0001c0001t0004g0050others(3): Show | 8 | HG01074.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+3590_-16+3592d others(5): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109544033 | |||||
chr8:109544067
|
C | T | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+3606C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544067 | ||||||
chr8:109544156
|
A | C | 1 | a0001c0001t0001g0115 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-16+3695A>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544156 | ||||||
chr8:109544205
|
T | G | 1 | a0001c0001t0003g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-16+3744T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544205 | ||||||
chr8:109544243
|
C | A | 1 | a0001c0001t0016g0085 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-16+3782C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544243 | ||||||
chr8:109544290
|
G | A | 43 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0032others(40): Show | 57 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.-16+3829G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544290 | ||||||
chr8:109544654
|
G | C | 55 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0009others(52): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-16+4193G>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544654 | ||||||
chr8:109544810
|
C | G | 1 | a0001c0001t0019g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+4349C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544810 | ||||||
chr8:109544855
|
T | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0077 | 5 | HG01261.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+4394T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544855 | ||||||
chr8:109544952
|
A | G | 16 | a0001c0001t0002g0015a0001c0001t0002g0048a0001c0001t0002g0180others(13): Show | 20 | HG00741.hp2 HG02615.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-16+4491A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109544952 | ||||||
chr8:109545120
|
G | C | 1 | a0001c0001t0002g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-16+4659G>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545120 | ||||||
chr8:109545187
|
T | G | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+4726T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545187 | ||||||
chr8:109545222
|
TGA | T | 8 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0033others(5): Show | 13 | HG00733.hp2 HG01074.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16+4764_-16+4765d others(4): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109545222 | |||||
chr8:109545253
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-16+4792C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545253 | ||||||
chr8:109545263
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-16+4802G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545263 | ||||||
chr8:109545267
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0124 | 2 | NA18952.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-16+4806A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545267 | ||||||
chr8:109545302
|
A | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 6 | HG01934.hp2 HG02132.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+4841A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545302 | ||||||
chr8:109545321
|
C | CA | 50 | a0001c0001t0001g0011a0001c0001t0001g0040a0001c0001t0001g0089others(47): Show | 69 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-16+4881dupA | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109545321 | |||||
chr8:109545321
|
C | CAA | 7 | a0001c0001t0002g0010a0001c0001t0002g0067a0001c0001t0002g0077others(4): Show | 10 | HG01261.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+4880_-16+4881d others(4): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109545321 | |||||
chr8:109545321
|
C | CAAA | 4 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(1): Show | 6 | HG02109.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+4879_-16+4881d others(5): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109545321 | |||||
chr8:109545321
|
CA | C | 8 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0001t0001g0126others(5): Show | 11 | HG00099.hp1 HG00323.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+4881delA | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109545321 | |||||
chr8:109545321
|
CAAA | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0154a0001c0001t0003g0155others(2): Show | 10 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16+4879_-16+4881d others(5): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109545321 | |||||
chr8:109545360
|
C | A | 1 | a0001c0001t0003g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-16+4899C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545360 | ||||||
chr8:109545361
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-16+4900A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545361 | ||||||
chr8:109545386
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-16+4925T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545386 | ||||||
chr8:109545440
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-16+4979C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545440 | ||||||
chr8:109545450
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-16+4989G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545450 | ||||||
chr8:109545457
|
AG | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-16+4999delG | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109545457 | |||||
chr8:109545581
|
T | G | 1 | a0001c0001t0009g0043 | 2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+5120T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545581 | ||||||
chr8:109545599
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+5138G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545599 | ||||||
chr8:109545848
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-15-4962C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545848 | ||||||
chr8:109545852
|
T | C | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-4958T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545852 | ||||||
chr8:109545938
|
A | G | 4 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0081others(1): Show | 6 | HG00733.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4872A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109545938 | ||||||
chr8:109546189
|
T | G | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-4621T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109546189 | ||||||
chr8:109546366
|
C | A | 1 | a0001c0001t0002g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-15-4444C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109546366 | ||||||
chr8:109546393
|
C | A | 43 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0032others(40): Show | 57 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.-15-4417C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109546393 | ||||||
chr8:109546548
|
G | C | 2 | a0001c0001t0002g0196a0001c0001t0022g0198 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-15-4262G>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109546548 | ||||||
chr8:109546766
|
T | C | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15-4044T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109546766 | ||||||
chr8:109547034
|
A | AT | 16 | a0001c0001t0001g0156a0001c0001t0002g0015a0001c0001t0002g0048others(13): Show | 20 | HG00597.hp1 HG00741.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-3766dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109547034 | |||||
chr8:109547204
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-15-3606G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109547204 | ||||||
chr8:109547397
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15-3413T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109547397 | ||||||
chr8:109547484
|
C | CT | 13 | a0001c0001t0001g0021a0001c0001t0001g0136a0001c0001t0002g0015others(10): Show | 18 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15-3313dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109547484 | |||||
chr8:109547702
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-3108G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109547702 | ||||||
chr8:109547727
|
G | A | 1 | a0001c0001t0001g0035 | 2 | NA18972.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-15-3083G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109547727 | ||||||
chr8:109547844
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-2966A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109547844 | ||||||
chr8:109547914
|
G | A | 1 | a0001c0001t0020g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15-2896G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109547914 | ||||||
chr8:109548047
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-15-2763C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548047 | ||||||
chr8:109548065
|
C | T | 16 | a0001c0001t0002g0015a0001c0001t0002g0048a0001c0001t0002g0180others(13): Show | 20 | HG00741.hp2 HG02615.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-2745C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548065 | ||||||
chr8:109548177
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0090a0001c0001t0001g0109others(1): Show | 5 | HG00438.hp1 HG00558.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-2633A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548177 | ||||||
chr8:109548252
|
C | A | 1 | a0001c0001t0003g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15-2558C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548252 | ||||||
chr8:109548312
|
G | A | 1 | a0001c0001t0004g0050 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-15-2498G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548312 | ||||||
chr8:109548363
|
A | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0203 | 3 | HG02615.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-15-2447A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548363 | ||||||
chr8:109548412
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-15-2398G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548412 | ||||||
chr8:109548705
|
G | A | 1 | a0001c0001t0014g0145 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-15-2105G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548705 | ||||||
chr8:109548887
|
C | CT | 33 | a0001c0001t0001g0030a0001c0001t0001g0130a0001c0001t0001g0206others(30): Show | 45 | HG00741.hp2 HG01884.hp1 HG01934.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15-1906dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 109548887 | |||||
chr8:109548938
|
T | C | 1 | a0001c0001t0009g0043 | 2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-15-1872T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548938 | ||||||
chr8:109548971
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-15-1839G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109548971 | ||||||
chr8:109549291
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15-1519T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109549291 | ||||||
chr8:109549475
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-15-1335G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109549475 | ||||||
chr8:109549548
|
A | T | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15-1262A>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109549548 | ||||||
chr8:109549561
|
T | G | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15-1249T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109549561 | ||||||
chr8:109549776
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-15-1034T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109549776 | ||||||
chr8:109550045
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-15-765A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109550045 | ||||||
chr8:109550233
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15-577A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109550233 | ||||||
chr8:109550589
|
A | G | 5 | a0001c0001t0003g0014a0001c0001t0003g0160a0001c0001t0003g0164others(2): Show | 8 | HG00544.hp1 NA18945.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-221A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109550589 | ||||||
chr8:109550592
|
AAGGG | A | 5 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0044others(2): Show | 10 | HG00423.hp2 HG02027.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-217_-15-214del others(4): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109550592 | ||||||
chr8:109550710
|
T | C | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-100T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109550710 | ||||||
chr8:109550806
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.-15-4A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 1/6 | chr8 | 109550806 | ||||||
chr8:109551057
|
G | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0030others(155): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.83+150G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551057 | ||||||
chr8:109551061
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG00323.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.83+154C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551061 | ||||||
chr8:109551075
|
C | G | 6 | a0001c0001t0003g0012a0001c0001t0003g0142a0001c0001t0003g0143others(3): Show | 9 | HG01081.hp1 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+168C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551075 | ||||||
chr8:109551118
|
T | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0077a0001c0001t0002g0078others(3): Show | 9 | HG01261.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+211T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551118 | ||||||
chr8:109551339
|
T | A | 7 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0033others(4): Show | 12 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.83+432T>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551339 | ||||||
chr8:109551491
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.83+584G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551491 | ||||||
chr8:109551565
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.83+658A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551565 | ||||||
chr8:109551600
|
C | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0203 | 3 | HG02615.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.83+693C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551600 | ||||||
chr8:109551695
|
A | G | 137 | a0001c0001t0001g0030a0001c0001t0001g0126a0001c0001t0001g0170others(134): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.83+788A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551695 | ||||||
chr8:109551738
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83+831G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551738 | ||||||
chr8:109551784
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.83+877T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551784 | ||||||
chr8:109551788
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.83+881A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109551788 | ||||||
chr8:109551876
|
TA | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0207a0001c0001t0001g0208 | 5 | HG01934.hp2 HG02132.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+974delA | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 109551876 | |||||
chr8:109552067
|
A | G | 1 | a0001c0001t0014g0145 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.83+1160A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552067 | ||||||
chr8:109552180
|
A | G | 7 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0086others(4): Show | 9 | HG00597.hp2 HG02083.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+1273A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552180 | ||||||
chr8:109552234
|
T | C | 46 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0018others(43): Show | 62 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.83+1327T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552234 | ||||||
chr8:109552261
|
TA | T | 6 | a0001c0001t0001g0120a0001c0001t0002g0018a0001c0001t0002g0032others(3): Show | 9 | HG01074.hp1 HG01884.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+1370delA | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 109552261 | |||||
chr8:109552261
|
TAA | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(152): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.83+1369_83+1370del others(2): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 109552261 | |||||
chr8:109552261
|
TAAA | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 6 | HG01934.hp2 HG02132.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+1368_83+1370del others(3): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 109552261 | |||||
chr8:109552552
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.84-1313T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552552 | ||||||
chr8:109552629
|
G | T | 1 | a0001c0001t0001g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.84-1236G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552629 | ||||||
chr8:109552899
|
C | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0009others(52): Show | 95 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.84-966C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552899 | ||||||
chr8:109552908
|
C | T | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-957C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552908 | ||||||
chr8:109552947
|
C | G | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.84-918C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109552947 | ||||||
chr8:109553244
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.84-621A>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109553244 | ||||||
chr8:109553260
|
T | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0077 | 5 | HG01261.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-605T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109553260 | ||||||
chr8:109553313
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.84-552G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109553313 | ||||||
chr8:109553633
|
C | T | 5 | a0001c0001t0002g0048a0001c0001t0002g0190a0001c0001t0002g0191others(2): Show | 6 | HG00741.hp2 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-232C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | chr8 | 109553633 | ||||||
chr8:109553704
|
C | CT | 4 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0080others(1): Show | 7 | HG01074.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-153dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 109553704 | |||||
chr8:109553948
|
G | T | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.162+5G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 3/6 | chr8 | 109553948 | ||||||
chr8:109553955
|
T | G | 56 | a0001c0001t0002g0194a0001c0001t0003g0002a0001c0001t0003g0005others(53): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.162+12T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 3/6 | chr8 | 109553955 | ||||||
chr8:109554195
|
G | A | 1 | a0001c0001t0014g0145 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162+252G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 3/6 | chr8 | 109554195 | ||||||
chr8:109554259
|
G | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0080others(1): Show | 7 | HG01074.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+316G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 3/6 | chr8 | 109554259 | ||||||
chr8:109554429
|
C | A | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-300C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 3/6 | chr8 | 109554429 | ||||||
chr8:109554492
|
G | GT | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-231dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr8 | 109554492 | |||||
chr8:109555006
|
T | G | 1 | a0001c0001t0020g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.321+119T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555006 | ||||||
chr8:109555066
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0203 | 3 | HG02615.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.321+179G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555066 | ||||||
chr8:109555093
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.321+206C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555093 | ||||||
chr8:109555199
|
G | T | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+312G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555199 | ||||||
chr8:109555247
|
C | T | 4 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0080others(1): Show | 7 | HG01074.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.321+360C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555247 | ||||||
chr8:109555439
|
T | C | 2 | a0001c0001t0003g0147a0001c0001t0003g0149 | 2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.321+552T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555439 | ||||||
chr8:109555450
|
C | G | 1 | a0001c0001t0014g0145 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.321+563C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555450 | ||||||
chr8:109555501
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.321+614A>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555501 | ||||||
chr8:109555545
|
G | A | 141 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0036others(138): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.321+658G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555545 | ||||||
chr8:109555827
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+940A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555827 | ||||||
chr8:109555828
|
C | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.321+941C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555828 | ||||||
chr8:109555962
|
G | A | 1 | a0001c0001t0019g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.322-973G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109555962 | ||||||
chr8:109556178
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.322-757A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556178 | ||||||
chr8:109556191
|
C | T | 2 | a0001c0001t0002g0051a0001c0001t0002g0203 | 3 | HG02615.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.322-744C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556191 | ||||||
chr8:109556199
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.322-736C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556199 | ||||||
chr8:109556384
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.322-551G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556384 | ||||||
chr8:109556464
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322-471A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556464 | ||||||
chr8:109556493
|
G | C | 1 | a0001c0001t0009g0043 | 2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.322-442G>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556493 | ||||||
chr8:109556570
|
G | A | 1 | a0001c0001t0019g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.322-365G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556570 | ||||||
chr8:109556599
|
A | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0105a0001c0001t0001g0120others(1): Show | 6 | NA18977.hp1 NA18999.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-336A>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556599 | ||||||
chr8:109556639
|
T | C | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-296T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 4/6 | chr8 | 109556639 | ||||||
chr8:109557148
|
A | G | 1 | a0001c0001t0003g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.429+106A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557148 | ||||||
chr8:109557310
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0099 | 3 | HG01071.hp1 HG01074.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.429+268G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557310 | ||||||
chr8:109557418
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+376A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557418 | ||||||
chr8:109557421
|
C | T | 1 | a0001c0001t0001g0019 | 3 | HG01243.hp2 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.429+379C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557421 | ||||||
chr8:109557430
|
T | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0081 | 5 | HG01884.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+388T>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557430 | ||||||
chr8:109557484
|
C | G | 4 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0080others(1): Show | 7 | HG01074.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+442C>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557484 | ||||||
chr8:109557569
|
C | T | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+527C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557569 | ||||||
chr8:109557569
|
CATGCT | C | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+528_429+532del others(5): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557569 | ||||||
chr8:109557581
|
G | C | 1 | a0001c0001t0014g0145 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.429+539G>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557581 | ||||||
chr8:109557585
|
G | A | 1 | a0001c0001t0004g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.429+543G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557585 | ||||||
chr8:109557598
|
G | A | 135 | a0001c0001t0001g0030a0001c0001t0001g0206a0001c0001t0001g0207others(132): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.429+556G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557598 | ||||||
chr8:109557831
|
A | G | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(160): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.429+789A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557831 | ||||||
chr8:109557969
|
A | G | 2 | a0001c0001t0003g0141a0001c0001t0003g0144 | 2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.429+927A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109557969 | ||||||
chr8:109558232
|
A | G | 1 | a0001c0001t0014g0145 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.429+1190A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109558232 | ||||||
chr8:109558324
|
A | G | 1 | a0001c0001t0002g0192 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.429+1282A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109558324 | ||||||
chr8:109558435
|
GT | G | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.429+1399delT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 109558435 | |||||
chr8:109558610
|
A | G | 1 | a0001c0001t0003g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.429+1568A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109558610 | ||||||
chr8:109558675
|
A | G | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1633A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109558675 | ||||||
chr8:109558716
|
T | C | 2 | a0001c0001t0002g0051a0001c0001t0002g0203 | 3 | HG02615.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.429+1674T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109558716 | ||||||
chr8:109558973
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430-1865G>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109558973 | ||||||
chr8:109559033
|
TA | T | 117 | a0001c0001t0001g0030a0001c0001t0001g0126a0001c0001t0001g0170others(114): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.430-1797delA | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 109559033 | |||||
chr8:109559043
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.430-1795C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559043 | ||||||
chr8:109559278
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.430-1560G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559278 | ||||||
chr8:109559534
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0081 | 5 | HG01884.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-1304G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559534 | ||||||
chr8:109559594
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.430-1244T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559594 | ||||||
chr8:109559643
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.430-1195C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559643 | ||||||
chr8:109559664
|
A | C | 16 | a0001c0001t0002g0015a0001c0001t0002g0048a0001c0001t0002g0180others(13): Show | 20 | HG00741.hp2 HG02615.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-1174A>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559664 | ||||||
chr8:109559669
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430-1169G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559669 | ||||||
chr8:109559773
|
C | T | 2 | a0001c0001t0010g0088a0001c0001t0010g0131 | 2 | HG00621.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.430-1065C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559773 | ||||||
chr8:109559815
|
T | TA | 8 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(5): Show | 11 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-1012dupA | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 109559815 | |||||
chr8:109559823
|
A | G | 1 | a0001c0001t0008g0119 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.430-1015A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559823 | ||||||
chr8:109559826
|
A | G | 5 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0081others(2): Show | 7 | HG00733.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-1012A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559826 | ||||||
chr8:109559851
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.430-987A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109559851 | ||||||
chr8:109559978
|
AAC | A | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.430-858_430-857del others(2): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr8 | 109559978 | |||||
chr8:109560097
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.430-741C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109560097 | ||||||
chr8:109560172
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.430-666G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109560172 | ||||||
chr8:109560340
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430-498A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109560340 | ||||||
chr8:109560604
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.430-234A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109560604 | ||||||
chr8:109560729
|
T | C | 1 | a0001c0001t0004g0202 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.430-109T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109560729 | ||||||
chr8:109560796
|
A | T | 1 | a0001c0001t0002g0071 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430-42A>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 5/6 | chr8 | 109560796 | ||||||
chr8:109561004
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.521+75G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561004 | ||||||
chr8:109561170
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0185 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.521+241G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561170 | ||||||
chr8:109561215
|
T | TTA | 8 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0081others(5): Show | 12 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.521+301_521+302dup others(2): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109561215 | |||||
chr8:109561384
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0137 | 2 | HG01952.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.521+455A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561384 | ||||||
chr8:109561541
|
A | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0187 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.521+612A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561541 | ||||||
chr8:109561629
|
TCATA | T | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.521+704_521+707del others(4): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109561629 | |||||
chr8:109561671
|
AT | A | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.521+749delT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109561671 | |||||
chr8:109561753
|
G | T | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.521+824G>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561753 | ||||||
chr8:109561867
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0081 | 5 | HG01884.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.521+938T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561867 | ||||||
chr8:109561890
|
C | CT | 43 | a0001c0001t0001g0021a0001c0001t0001g0109a0001c0001t0001g0126others(40): Show | 54 | HG00733.hp2 HG01109.hp2 HG01261.hp2 others(51): Show |
intron_variant | MODIFIER | c.521+980dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109561890 | |||||
chr8:109561890
|
C | CTT | 4 | a0001c0001t0002g0018a0001c0001t0002g0034a0001c0001t0002g0080others(1): Show | 7 | HG01074.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+979_521+980dup others(2): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109561890 | |||||
chr8:109561890
|
CT | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0106a0001c0001t0001g0135others(4): Show | 7 | HG01069.hp1 HG01069.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+980delT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109561890 | |||||
chr8:109561891
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.521+962T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561891 | ||||||
chr8:109561924
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0081 | 5 | HG01884.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.521+995G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109561924 | ||||||
chr8:109562053
|
C | A | 16 | a0001c0001t0002g0015a0001c0001t0002g0048a0001c0001t0002g0180others(13): Show | 20 | HG00741.hp2 HG02615.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.521+1124C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109562053 | ||||||
chr8:109562357
|
C | A | 2 | a0001c0001t0002g0191a0001c0001t0002g0193 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.521+1428C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109562357 | ||||||
chr8:109562836
|
A | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0203 | 3 | HG02615.hp2 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.522-1603A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109562836 | ||||||
chr8:109562943
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.522-1496C>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109562943 | ||||||
chr8:109563174
|
A | G | 1 | a0001c0001t0003g0168 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.522-1265A>G | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109563174 | ||||||
chr8:109563577
|
C | CT | 5 | a0001c0001t0004g0029a0001c0001t0004g0050a0001c0001t0004g0201others(2): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.522-846dupT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109563577 | |||||
chr8:109563577
|
CT | C | 25 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0102others(22): Show | 28 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.522-846delT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109563577 | |||||
chr8:109563641
|
C | T | 43 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0032others(40): Show | 57 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.522-798C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109563641 | ||||||
chr8:109563649
|
CAT | C | 13 | a0001c0001t0003g0012a0001c0001t0003g0024a0001c0001t0003g0076others(10): Show | 18 | HG00621.hp2 HG01081.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.522-789_522-788del others(2): Show |
EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109563649 | ||||||
chr8:109563712
|
T | A | 25 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0016others(22): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.522-727T>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109563712 | ||||||
chr8:109563734
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0122others(1): Show | 9 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.522-705C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109563734 | ||||||
chr8:109563736
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.522-703C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109563736 | ||||||
chr8:109563869
|
C | T | 3 | a0001c0001t0005g0031a0001c0001t0005g0052a0001c0001t0005g0053 | 4 | HG02572.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.522-570C>T | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109563869 | ||||||
chr8:109563942
|
CT | C | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.522-492delT | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 109563942 | |||||
chr8:109564091
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.522-348T>C | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109564091 | ||||||
chr8:109564427
|
G | A | 8 | a0001c0001t0002g0049a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.522-12G>A | EBAG9 | ENSG00000147654.16 | transcript | ENST00000337573.10 | protein_coding | 6/6 | chr8 | 109564427 |