geneid | 3638 |
---|---|
ensemblid | ENSG00000186480.13 |
hgncid | 6083 |
symbol | INSIG1 |
name | insulin induced gene 1 |
refseq_nuc | NM_005542.6 |
refseq_prot | NP_005533.2 |
ensembl_nuc | ENST00000340368.9 |
ensembl_prot | ENSP00000344741.4 |
mane_status | MANE Select |
chr | chr7 |
start | 155297878 |
end | 155310235 |
strand | + |
ver | v1.2 |
region | chr7:155297878-155310235 |
region5000 | chr7:155292878-155315235 |
regionname0 | INSIG1_chr7_155297878_155310235 |
regionname5000 | INSIG1_chr7_155292878_155315235 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 277 | 441 | 96 | 76 | 215 | 18 | 34 | 173 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0002 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0003 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0004 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 834 | 432 | 90 | 73 | 215 | 18 | 34 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
c0002 | 0/0 | 834 | 8 | 5 | 3 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
c0003 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
c0004 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
c0005 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
c0006 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2075 | 315 | 57 | 68 | 151 | 16 | 22 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0002 | 0/0 | 2076 | 41 | 10 | 2 | 22 | 1 | 6 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0003 | 0/0 | 2075 | 32 | 2 | 0 | 29 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0004 | 0/0 | 2075 | 11 | 0 | 0 | 11 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0005 | 0/0 | 2075 | 8 | 8 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0006 | 0/0 | 2073 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0007 | 0/0 | 2075 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0008 | 0/1 | 2075 | 4 | 0 | 1 | 0 | 1 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0009 | 0/0 | 2075 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0010 | 0/0 | 2069 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0011 | 0/0 | 2076 | 2 | 0 | 0 | 0 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0012 | 0/0 | 2075 | 2 | 1 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0013 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0014 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0015 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0016 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0017 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0018 | 0/0 | 2075 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0019 | 0/0 | 2075 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0020 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0021 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0022 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0023 | 0/0 | 2075 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0024 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0025 | 0/0 | 2075 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0026 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
t0027 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 57 | 0 | 7 | 43 | 1 | 6 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0002 | 0/0 | 37 | 3 | 7 | 26 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0003 | 0/0 | 33 | 0 | 0 | 31 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0004 | 0/0 | 28 | 4 | 2 | 15 | 1 | 6 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0005 | 1/0 | 23 | 0 | 0 | 22 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0006 | 0/0 | 20 | 3 | 11 | 0 | 3 | 3 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0007 | 0/0 | 20 | 1 | 16 | 0 | 2 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0008 | 0/0 | 19 | 0 | 13 | 0 | 3 | 3 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0009 | 0/0 | 15 | 3 | 0 | 12 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0015 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0018 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0019 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0022 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0023 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0026 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0027 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0030 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 834 | 432 | 90 | 73 | 215 | 18 | 34 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0002 | 0/0 | 834 | 8 | 5 | 3 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0004 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0002c0003 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0003c0005 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0004c0006 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2908 | 310 | 56 | 66 | 149 | 16 | 22 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0002 | 0/0 | 2909 | 40 | 9 | 2 | 22 | 1 | 6 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0003 | 0/0 | 2908 | 31 | 2 | 0 | 28 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0004 | 0/0 | 2908 | 11 | 0 | 0 | 11 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0005 | 0/0 | 2908 | 8 | 8 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0006 | 0/0 | 2906 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0007 | 0/0 | 2908 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0008 | 0/1 | 2908 | 4 | 0 | 1 | 0 | 1 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0009 | 0/0 | 2908 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0011 | 0/0 | 2909 | 2 | 0 | 0 | 0 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0012 | 0/0 | 2908 | 2 | 1 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0014 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0015 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0016 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0017 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0018 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0019 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0020 | 0/0 | 2984 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0021 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0022 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0023 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0024 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0025 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0026 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0001t0027 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0002t0001 | 0/0 | 2908 | 3 | 1 | 2 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0002t0006 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0002t0010 | 0/0 | 2902 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0002t0013 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0001c0004t0002 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0002c0003t0001 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0003c0005t0003 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
a0004c0006t0001 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | copy fasta | chr7 | 155292878 | 155315235 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 47 | 0 | 7 | 33 | 1 | 6 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0002 | 0/0 | 32 | 2 | 6 | 23 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0003 | 0/0 | 32 | 0 | 0 | 30 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0005 | 1/0 | 22 | 0 | 0 | 21 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0006 | 0/0 | 18 | 2 | 10 | 0 | 3 | 3 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0007 | 0/0 | 19 | 1 | 15 | 0 | 2 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0008 | 0/0 | 18 | 0 | 13 | 0 | 3 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0030 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0004 | 0/0 | 26 | 4 | 2 | 15 | 1 | 4 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0009 | 0/0 | 13 | 1 | 0 | 12 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0015 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0004g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0005g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0007g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0008g0022 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0008g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0009g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0009g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0011g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0012g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0015g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0016g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0017g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0018g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0019g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0021g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0023g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0025g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0026g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0001t0027g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0002t0001g0027 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0002t0010g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0002t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0002t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0001c0004t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0002c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0003c0005t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
a0004c0006t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00280 | hp1 | a0001 | c0001 | t0008 | g0022 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00597 | hp1 | a0001 | c0001 | t0015 | g0002 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00673 | hp1 | a0004 | c0006 | t0001 | g0005 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0104 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01361 | hp1 | a0001 | c0001 | t0023 | g0006 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01891 | hp2 | a0001 | c0002 | t0010 | g0072 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01934 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01952 | hp1 | a0001 | c0002 | t0010 | g0019 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02015 | hp2 | a0001 | c0001 | t0014 | g0002 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02258 | hp1 | a0001 | c0001 | t0017 | g0056 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02273 | hp2 | a0001 | c0001 | t0019 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02630 | hp1 | a0001 | c0004 | t0002 | g0091 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0002 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02683 | hp1 | a0001 | c0001 | t0008 | g0022 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02818 | hp2 | a0001 | c0001 | t0021 | g0076 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02965 | hp1 | a0001 | c0002 | t0010 | g0019 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03139 | hp2 | a0001 | c0002 | t0006 | g0019 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0024 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03453 | hp1 | a0001 | c0002 | t0013 | g0019 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03540 | hp1 | a0001 | c0001 | t0026 | g0006 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03927 | hp2 | a0001 | c0001 | t0011 | g0004 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03942 | hp2 | a0001 | c0001 | t0018 | g0008 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18947 | hp2 | a0001 | c0001 | t0016 | g0111 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18987 | hp2 | a0003 | c0005 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18989 | hp1 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19087 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20905 | hp1 | a0001 | c0001 | t0011 | g0004 | SAS | GIH | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20905 | hp2 | a0001 | c0001 | t0025 | g0026 | SAS | GIH | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02559 | hp1 | a0001 | c0001 | t0022 | g0124 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA20300 | hp2 | a0001 | c0001 | t0027 | g0042 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0023 | REF | REF | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:155298385
|
G | A | 1 | a0002 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.100G>A | p.Val34Ile | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 209/2908 | 100/834 | 34/277 | chr7 | 155298385 | ||
chr7:155298529
|
C | T | 1 | a0004 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.244C>T | p.His82Tyr | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 353/2908 | 244/834 | 82/277 | chr7 | 155298529 | ||
chr7:155301671
|
G | T | 1 | a0003 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.518G>T | p.Gly173Val | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/6 | 627/2908 | 518/834 | 173/277 | chr7 | 155301671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:155298621
|
T | A | 1 | a0001c0004 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.336T>A | p.Thr112Thr | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 445/2908 | 336/834 | 112/277 | chr7 | 155298621 | ||
chr7:155302843
|
T | C | 1 | a0001c0002 | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(5): Show |
synonymous_variant | LOW | c.801T>C | p.Ala267Ala | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/6 | 910/2908 | 801/834 | 267/277 | chr7 | 155302843 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:155297906
|
T | C | 1 | a0001c0001t0004 | 11 | NA18941.hp1 NA18949.hp2 NA18954.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-81T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/6 | 380 | chr7 | 155297906 | |||||
chr7:155297925
|
T | C | 1 | a0001c0001t0009 | 3 | HG01109.hp2 HG02717.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-62T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/6 | 361 | chr7 | 155297925 | |||||
chr7:155298268
|
C | T | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 18 | chr7 | 155298268 | |||||
chr7:155308359
|
G | A | 4 | a0001c0001t0006a0001c0002t0006a0001c0002t0010others(1): Show | 8 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*89G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 89 | chr7 | 155308359 | |||||
chr7:155308613
|
A | C | 1 | a0001c0001t0026 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*343A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 343 | chr7 | 155308613 | |||||
chr7:155308688
|
G | A | 1 | a0001c0001t0007 | 4 | HG02965.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 418 | chr7 | 155308688 | |||||
chr7:155308712
|
A | G | 1 | a0001c0001t0025 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*442A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 442 | chr7 | 155308712 | |||||
chr7:155308738
|
T | TA | 3 | a0001c0001t0002a0001c0001t0011a0001c0004t0002 | 43 | HG01074.hp1 HG01361.hp2 HG02074.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*479dupA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 480 | INFO_REALIGN_3_PRIME | chr7 | 155308738 | ||||
chr7:155308739
|
A | T | 1 | a0001c0001t0024 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*469A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 469 | chr7 | 155308739 | |||||
chr7:155308745
|
A | C | 1 | a0001c0001t0023 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*475A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 475 | chr7 | 155308745 | |||||
chr7:155308748
|
AAC | A | 3 | a0001c0001t0006a0001c0002t0006a0001c0002t0010 | 7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*480_*481delCA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 480 | INFO_REALIGN_3_PRIME | chr7 | 155308748 | ||||
chr7:155308751
|
A | C | 3 | a0001c0001t0006a0001c0002t0006a0001c0002t0010 | 7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*481A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 481 | chr7 | 155308751 | |||||
chr7:155308805
|
G | A | 2 | a0001c0001t0014a0001c0001t0015 | 2 | HG00597.hp1 HG02015.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 535 | chr7 | 155308805 | |||||
chr7:155308807
|
C | T | 1 | a0001c0001t0022 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 537 | chr7 | 155308807 | |||||
chr7:155308828
|
C | T | 2 | a0001c0001t0005a0001c0001t0027 | 9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*558C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 558 | chr7 | 155308828 | |||||
chr7:155308836
|
C | T | 1 | a0001c0001t0021 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*566C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 566 | chr7 | 155308836 | |||||
chr7:155308859
|
T | C | 3 | a0001c0001t0006a0001c0002t0006a0001c0002t0010 | 7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*589T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 589 | chr7 | 155308859 | |||||
chr7:155308909
|
C | T | 1 | a0001c0001t0012 | 2 | HG01934.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*639C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 639 | chr7 | 155308909 | |||||
chr7:155308975
|
G | A | 2 | a0001c0001t0003a0003c0005t0003 | 32 | HG00673.hp2 HG02027.hp2 HG02074.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 705 | chr7 | 155308975 | |||||
chr7:155309001
|
T | A | 3 | a0001c0001t0006a0001c0002t0006a0001c0002t0010 | 7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*731T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 731 | chr7 | 155309001 | |||||
chr7:155309073
|
A | AGCCAAAA others(69): Show |
1 | a0001c0001t0020 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805_*880dupCCAAAA others(70): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 881 | INFO_REALIGN_3_PRIME | chr7 | 155309073 | ||||
chr7:155309078
|
A | G | 1 | a0001c0001t0011 | 2 | HG03927.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*808A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 808 | chr7 | 155309078 | |||||
chr7:155309288
|
AACTT | A | 1 | a0001c0002t0010 | 3 | HG01891.hp2 HG01952.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1019_*1022delACTT | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1019 | chr7 | 155309288 | |||||
chr7:155309455
|
C | A | 1 | a0001c0001t0022 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1185C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1185 | chr7 | 155309455 | |||||
chr7:155309495
|
T | C | 1 | a0001c0001t0016 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1225 | chr7 | 155309495 | |||||
chr7:155309505
|
G | A | 3 | a0001c0001t0006a0001c0002t0006a0001c0002t0010 | 7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1235G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1235 | chr7 | 155309505 | |||||
chr7:155309756
|
T | C | 1 | a0001c0001t0017 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1486T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1486 | chr7 | 155309756 | |||||
chr7:155309791
|
A | T | 1 | a0001c0001t0015 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1521 | chr7 | 155309791 | |||||
chr7:155309823
|
A | G | 1 | a0001c0001t0008 | 4 | HG00280.hp1 HG01099.hp1 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1553A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1553 | chr7 | 155309823 | |||||
chr7:155309839
|
T | C | 1 | a0001c0001t0020 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1569T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1569 | chr7 | 155309839 | |||||
chr7:155309870
|
T | A | 1 | a0001c0001t0018 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1600 | chr7 | 155309870 | |||||
chr7:155310111
|
T | C | 1 | a0001c0001t0019 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1841T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1841 | chr7 | 155310111 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:155297979
|
A | T | 1 | a0001c0001t0001g0040 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-28+20A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155297979 | ||||||
chr7:155297979
|
AG | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0030others(19): Show | 60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-28+24delG | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 155297979 | |||||
chr7:155297991
|
C | G | 1 | a0001c0001t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-28+32C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155297991 | ||||||
chr7:155298065
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0125 | 2 | HG00558.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-28+106G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155298065 | ||||||
chr7:155298120
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-27-139C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155298120 | ||||||
chr7:155298255
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA18939.hp2 | splice_region_variant&intron_variant | LOW | c.-27-4C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155298255 | ||||||
chr7:155298852
|
G | T | 5 | a0001c0001t0003g0012a0001c0001t0003g0015a0001c0001t0003g0038others(2): Show | 14 | HG03834.hp2 NA18939.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.412+155G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155298852 | ||||||
chr7:155298896
|
C | G | 1 | a0001c0001t0001g0029 | 3 | HG01891.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.412+199C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155298896 | ||||||
chr7:155298932
|
A | G | 30 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0089others(27): Show | 82 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.412+235A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155298932 | ||||||
chr7:155299146
|
T | G | 1 | a0001c0001t0003g0108 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.412+449T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299146 | ||||||
chr7:155299235
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+538C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299235 | ||||||
chr7:155299302
|
G | C | 1 | a0001c0001t0016g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.412+605G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299302 | ||||||
chr7:155299357
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+660A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299357 | ||||||
chr7:155299539
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.412+842C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299539 | ||||||
chr7:155299595
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0086others(1): Show | 9 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.412+898A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299595 | ||||||
chr7:155299696
|
G | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0099others(26): Show | 81 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.412+999G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299696 | ||||||
chr7:155299836
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.412+1139A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299836 | ||||||
chr7:155299869
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0023others(29): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.412+1172T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299869 | ||||||
chr7:155299961
|
C | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0030others(19): Show | 60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.412+1264C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299961 | ||||||
chr7:155299968
|
G | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0030others(19): Show | 60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.412+1271G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299968 | ||||||
chr7:155300007
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.412+1310G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300007 | ||||||
chr7:155300043
|
A | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.412+1346A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300043 | ||||||
chr7:155300046
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.412+1349C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300046 | ||||||
chr7:155300090
|
C | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0030others(18): Show | 59 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.412+1393C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300090 | ||||||
chr7:155300181
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.413-1385T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300181 | ||||||
chr7:155300229
|
G | C | 4 | a0001c0001t0001g0031a0001c0001t0005g0010a0001c0001t0005g0043others(1): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-1337G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300229 | ||||||
chr7:155300244
|
CTG | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0005g0010others(3): Show | 19 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.413-1321_413-1320d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300244 | ||||||
chr7:155300377
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.413-1189G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300377 | ||||||
chr7:155300392
|
C | G | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.413-1174C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300392 | ||||||
chr7:155300432
|
C | CTG | 28 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0030others(25): Show | 69 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.413-1134_413-1133i others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300432 | ||||||
chr7:155300436
|
A | AT | 28 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0030others(25): Show | 69 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.413-1124dupT | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 155300436 | |||||
chr7:155300495
|
T | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.413-1071T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300495 | ||||||
chr7:155300511
|
A | G | 5 | a0001c0002t0001g0027a0001c0002t0006g0019a0001c0002t0010g0019others(2): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-1055A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300511 | ||||||
chr7:155300515
|
C | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.413-1051C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300515 | ||||||
chr7:155300608
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.413-958C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300608 | ||||||
chr7:155300701
|
G | A | 29 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0099others(26): Show | 81 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.413-865G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300701 | ||||||
chr7:155300730
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0070 | 3 | NA18973.hp1 NA19007.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.413-836A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300730 | ||||||
chr7:155300778
|
A | T | 2 | a0001c0001t0003g0088a0001c0001t0022g0124 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.413-788A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300778 | ||||||
chr7:155300863
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0074 | 5 | HG02109.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-703T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300863 | ||||||
chr7:155300872
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.413-694C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300872 | ||||||
chr7:155300916
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.413-650C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300916 | ||||||
chr7:155300924
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(53): Show | 150 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.413-642G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300924 | ||||||
chr7:155301008
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.413-558C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301008 | ||||||
chr7:155301029
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0020others(14): Show | 44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.413-537C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301029 | ||||||
chr7:155301069
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.413-497C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301069 | ||||||
chr7:155301332
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.413-234C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301332 | ||||||
chr7:155301364
|
TA | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0068a0001c0001t0005g0010others(2): Show | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-196delA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 155301364 | |||||
chr7:155301377
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.413-189C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301377 | ||||||
chr7:155301544
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.413-22A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301544 | ||||||
chr7:155301756
|
T | G | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.537+66T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301756 | ||||||
chr7:155301864
|
T | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0037others(36): Show | 101 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(98): Show |
intron_variant | MODIFIER | c.537+174T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301864 | ||||||
chr7:155301904
|
T | A | 1 | a0001c0001t0004g0049 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.537+214T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301904 | ||||||
chr7:155301925
|
T | TTA | 3 | a0001c0001t0001g0014a0001c0001t0001g0086a0001c0001t0007g0014 | 6 | HG01884.hp1 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+243_537+244dup others(2): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 155301925 | |||||
chr7:155301933
|
A | T | 1 | a0001c0001t0006g0079 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.537+243A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301933 | ||||||
chr7:155301940
|
A | AAT | 99 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.537+258_537+259dup others(2): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 155301940 | |||||
chr7:155301955
|
T | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0099others(26): Show | 81 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.537+265T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301955 | ||||||
chr7:155302116
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.538-135T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302116 | ||||||
chr7:155302125
|
G | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 5 | HG02109.hp1 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-126G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302125 | ||||||
chr7:155302149
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 5 | HG02109.hp1 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-102G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302149 | ||||||
chr7:155302196
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0086a0001c0001t0007g0014 | 6 | HG01884.hp1 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-55G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302196 | ||||||
chr7:155302215
|
A | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0030others(18): Show | 59 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.538-36A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302215 | ||||||
chr7:155302438
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.704+21A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302438 | ||||||
chr7:155302462
|
C | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(10): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.704+45C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302462 | ||||||
chr7:155302555
|
A | T | 1 | a0001c0001t0002g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.704+138A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302555 | ||||||
chr7:155302632
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.705-115C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302632 | ||||||
chr7:155302674
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.705-73A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302674 | ||||||
chr7:155302882
|
C | T | 38 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0037others(35): Show | 100 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(97): Show |
intron_variant | MODIFIER | c.804+36C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155302882 | ||||||
chr7:155302883
|
G | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 30 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.804+37G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155302883 | ||||||
chr7:155303340
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0077others(4): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+494G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303340 | ||||||
chr7:155303365
|
T | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0037others(35): Show | 98 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(95): Show |
intron_variant | MODIFIER | c.804+519T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303365 | ||||||
chr7:155303483
|
G | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.804+637G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303483 | ||||||
chr7:155303541
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.804+695C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303541 | ||||||
chr7:155303542
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0077others(4): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+696G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303542 | ||||||
chr7:155303576
|
G | A | 4 | a0001c0001t0001g0031a0001c0001t0005g0010a0001c0001t0005g0043others(1): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.804+730G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303576 | ||||||
chr7:155303660
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+814A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303660 | ||||||
chr7:155303726
|
C | A | 37 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0037others(34): Show | 97 | HG00673.hp2 HG01074.hp1 HG01361.hp2 others(94): Show |
intron_variant | MODIFIER | c.804+880C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303726 | ||||||
chr7:155303742
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0008g0022a0001c0001t0008g0023 | 6 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+896C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303742 | ||||||
chr7:155303976
|
C | CT | 7 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0040others(4): Show | 12 | HG00438.hp1 HG01123.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+1152dupT | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | |||||
chr7:155303976
|
CTT | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0051others(8): Show | 18 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.804+1151_804+1152d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | |||||
chr7:155303976
|
CTTT | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(49): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.804+1150_804+1152d others(5): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | |||||
chr7:155303976
|
CTTTT | C | 36 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0037others(33): Show | 89 | HG00673.hp2 HG01074.hp1 HG01168.hp1 others(86): Show |
intron_variant | MODIFIER | c.804+1149_804+1152d others(6): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | |||||
chr7:155304083
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0005g0010a0001c0001t0005g0043others(1): Show | 11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.804+1237C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304083 | ||||||
chr7:155304175
|
G | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0086a0001c0001t0007g0014 | 6 | HG01884.hp1 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1329G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304175 | ||||||
chr7:155304214
|
T | G | 5 | a0001c0001t0001g0031a0001c0001t0005g0010a0001c0001t0005g0043others(2): Show | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+1368T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304214 | ||||||
chr7:155304234
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.804+1388G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304234 | ||||||
chr7:155304389
|
T | G | 28 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0099others(25): Show | 80 | HG00673.hp2 HG01074.hp1 HG01361.hp2 others(77): Show |
intron_variant | MODIFIER | c.804+1543T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304389 | ||||||
chr7:155304405
|
G | A | 1 | a0001c0002t0001g0027 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.804+1559G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304405 | ||||||
chr7:155304484
|
A | T | 2 | a0001c0001t0006g0045a0001c0001t0006g0079 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.804+1638A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304484 | ||||||
chr7:155304567
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.804+1721G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304567 | ||||||
chr7:155304619
|
A | C | 4 | a0001c0002t0006g0019a0001c0002t0010g0019a0001c0002t0010g0072others(1): Show | 5 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1773A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304619 | ||||||
chr7:155304642
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1796G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304642 | ||||||
chr7:155304659
|
T | C | 1 | a0001c0001t0002g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.804+1813T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304659 | ||||||
chr7:155304818
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.804+1972T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304818 | ||||||
chr7:155304865
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+2019C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304865 | ||||||
chr7:155304876
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.804+2030G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304876 | ||||||
chr7:155304937
|
A | G | 4 | a0001c0002t0006g0019a0001c0002t0010g0019a0001c0002t0010g0072others(1): Show | 5 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2091A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304937 | ||||||
chr7:155304981
|
C | CA | 11 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0061others(8): Show | 17 | HG00408.hp1 HG01123.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.804+2151dupA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155304981 | |||||
chr7:155304981
|
C | CAA | 61 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.804+2150_804+2151d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155304981 | |||||
chr7:155304981
|
C | CAAA | 19 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0074others(16): Show | 43 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.804+2149_804+2151d others(5): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155304981 | |||||
chr7:155305071
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+2225G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305071 | ||||||
chr7:155305107
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.804+2261C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305107 | ||||||
chr7:155305145
|
C | CA | 33 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0024others(30): Show | 73 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.804+2316dupA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155305145 | |||||
chr7:155305145
|
C | CAA | 6 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 8 | HG01433.hp1 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+2315_804+2316d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155305145 | |||||
chr7:155305157
|
A | C | 2 | a0001c0001t0001g0023a0001c0001t0008g0023 | 3 | HG00140.hp2 HG02145.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.804+2311A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305157 | ||||||
chr7:155305200
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.804+2354G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305200 | ||||||
chr7:155305207
|
T | C | 3 | a0001c0001t0005g0010a0001c0001t0005g0043a0001c0001t0027g0042 | 9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+2361T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305207 | ||||||
chr7:155305223
|
C | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0077others(4): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+2377C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305223 | ||||||
chr7:155305256
|
T | C | 4 | a0001c0002t0006g0019a0001c0002t0010g0019a0001c0002t0010g0072others(1): Show | 5 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2410T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305256 | ||||||
chr7:155305357
|
G | A | 6 | a0001c0001t0006g0044a0001c0001t0017g0056a0001c0002t0006g0019others(3): Show | 7 | HG01891.hp2 HG01952.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+2511G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305357 | ||||||
chr7:155305462
|
A | T | 3 | a0001c0001t0005g0010a0001c0001t0005g0043a0001c0001t0027g0042 | 9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+2616A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305462 | ||||||
chr7:155305506
|
A | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(14): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.804+2660A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305506 | ||||||
chr7:155305512
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0063 | 2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.804+2666G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305512 | ||||||
chr7:155305574
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.805-2667A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305574 | ||||||
chr7:155305652
|
A | G | 3 | a0001c0001t0005g0010a0001c0001t0005g0043a0001c0001t0027g0042 | 9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.805-2589A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305652 | ||||||
chr7:155305669
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2572C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305669 | ||||||
chr7:155305918
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0080 | 4 | HG01258.hp1 HG01261.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2323G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305918 | ||||||
chr7:155305933
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.805-2308C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305933 | ||||||
chr7:155305977
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0008g0022a0001c0001t0008g0023 | 6 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-2264T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305977 | ||||||
chr7:155306071
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.805-2170C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306071 | ||||||
chr7:155306095
|
G | T | 5 | a0001c0001t0006g0044a0001c0002t0006g0019a0001c0002t0010g0019others(2): Show | 6 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-2146G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306095 | ||||||
chr7:155306451
|
T | C | 5 | a0001c0001t0006g0044a0001c0002t0006g0019a0001c0002t0010g0019others(2): Show | 6 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-1790T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306451 | ||||||
chr7:155306624
|
G | A | 1 | a0001c0002t0001g0027 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.805-1617G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306624 | ||||||
chr7:155306662
|
T | A | 1 | a0001c0001t0001g0017 | 4 | NA18956.hp1 NA18957.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1579T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306662 | ||||||
chr7:155306671
|
T | TAGAAACT others(21): Show |
1 | a0001c0001t0002g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.805-1569_805-1542d others(30): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155306671 | |||||
chr7:155306767
|
G | A | 5 | a0001c0001t0006g0044a0001c0002t0006g0019a0001c0002t0010g0019others(2): Show | 6 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-1474G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306767 | ||||||
chr7:155306775
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.805-1466C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306775 | ||||||
chr7:155306814
|
AC | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 31 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.805-1425delC | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155306814 | |||||
chr7:155306857
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0017g0056 | 6 | HG02258.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-1384G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306857 | ||||||
chr7:155306928
|
G | T | 14 | a0001c0001t0002g0004a0001c0001t0002g0021a0001c0001t0002g0090others(11): Show | 43 | HG01074.hp1 HG01361.hp2 HG02074.hp1 others(40): Show |
intron_variant | MODIFIER | c.805-1313G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306928 | ||||||
chr7:155306948
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0109others(10): Show | 46 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.805-1293G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306948 | ||||||
chr7:155306987
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.805-1254C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306987 | ||||||
chr7:155306990
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.805-1251T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306990 | ||||||
chr7:155307002
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0086others(2): Show | 12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.805-1239T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307002 | ||||||
chr7:155307011
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.805-1230C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307011 | ||||||
chr7:155307154
|
A | C | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0079others(4): Show | 8 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-1087A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307154 | ||||||
chr7:155307399
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0085 | 3 | NA18967.hp1 NA18980.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.805-842G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307399 | ||||||
chr7:155307420
|
G | A | 7 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0079others(4): Show | 8 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-821G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307420 | ||||||
chr7:155307432
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0080others(4): Show | 27 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.805-809T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307432 | ||||||
chr7:155307466
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.805-775G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307466 | ||||||
chr7:155307538
|
T | G | 1 | a0001c0001t0002g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.805-703T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307538 | ||||||
chr7:155307579
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.805-662A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307579 | ||||||
chr7:155307601
|
T | C | 1 | a0001c0001t0001g0037 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.805-640T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307601 | ||||||
chr7:155307636
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.805-605A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307636 | ||||||
chr7:155307797
|
A | T | 14 | a0001c0001t0002g0004a0001c0001t0002g0021a0001c0001t0002g0090others(11): Show | 43 | HG01074.hp1 HG01361.hp2 HG02074.hp1 others(40): Show |
intron_variant | MODIFIER | c.805-444A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307797 | ||||||
chr7:155307810
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.805-431A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307810 | ||||||
chr7:155307902
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0026others(23): Show | 88 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.805-339A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307902 | ||||||
chr7:155307927
|
T | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.805-314T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307927 | ||||||
chr7:155307940
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.805-301T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307940 | ||||||
chr7:155307945
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0077others(4): Show | 24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.805-296C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307945 | ||||||
chr7:155307946
|
A | G | 68 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.805-295A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307946 | ||||||
chr7:155308050
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0099 | 3 | HG00408.hp2 NA18971.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.805-191G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308050 | ||||||
chr7:155308052
|
T | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.805-189T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308052 | ||||||
chr7:155308053
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.805-188G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308053 | ||||||
chr7:155308078
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.805-163C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308078 | ||||||
chr7:155308082
|
C | G | 1 | a0001c0001t0022g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.805-159C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308082 | ||||||
chr7:155308129
|
C | A | 1 | a0001c0001t0005g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.805-112C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308129 | ||||||
chr7:155308143
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805-98A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308143 | ||||||
chr7:155308145
|
C | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(34): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.805-96C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308145 | ||||||
chr7:155308197
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0009g0024 | 3 | HG02717.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.805-44G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308197 |