geneid | 51141 |
---|---|
ensemblid | ENSG00000125629.16 |
hgncid | 20452 |
symbol | INSIG2 |
name | insulin induced gene 2 |
refseq_nuc | NM_016133.4 |
refseq_prot | NP_057217.2 |
ensembl_nuc | ENST00000245787.9 |
ensembl_prot | ENSP00000245787.4 |
mane_status | MANE Select |
chr | chr2 |
start | 118088471 |
end | 118110997 |
strand | + |
ver | v1.2 |
region | chr2:118088471-118110997 |
region5000 | chr2:118083471-118115997 |
regionname0 | INSIG2_chr2_118088471_118110997 |
regionname5000 | INSIG2_chr2_118083471_118115997 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 225 | 437 | 96 | 80 | 199 | 16 | 44 | 151 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0002 | 0/0 | 225 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0003 | 0/0 | 240 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 678 | 425 | 85 | 80 | 199 | 16 | 43 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
c0002 | 0/0 | 678 | 10 | 10 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
c0003 | 0/0 | 678 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
c0004 | 0/0 | 678 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
c0005 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
c0006 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2883 | 90 | 7 | 19 | 55 | 2 | 7 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0002 | 0/0 | 2886 | 84 | 15 | 5 | 60 | 0 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0003 | 0/0 | 2881 | 56 | 7 | 12 | 29 | 2 | 6 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0004 | 0/0 | 2882 | 53 | 31 | 9 | 4 | 2 | 7 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0005 | 0/0 | 2882 | 41 | 1 | 6 | 20 | 4 | 10 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0006 | 0/0 | 2885 | 15 | 12 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0007 | 0/0 | 2882 | 15 | 0 | 9 | 1 | 1 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0008 | 0/1 | 2885 | 9 | 2 | 6 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0009 | 0/0 | 2886 | 9 | 9 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0010 | 0/0 | 2881 | 7 | 0 | 1 | 6 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0011 | 0/0 | 2882 | 7 | 0 | 3 | 0 | 3 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0012 | 0/0 | 2883 | 7 | 3 | 1 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0013 | 0/0 | 2882 | 5 | 0 | 3 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0014 | 0/0 | 2884 | 4 | 1 | 2 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0015 | 0/0 | 2883 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0016 | 0/0 | 2882 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0017 | 0/0 | 2884 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0018 | 0/0 | 2883 | 4 | 0 | 0 | 3 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0019 | 0/0 | 2882 | 3 | 0 | 0 | 0 | 0 | 3 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0020 | 0/0 | 2879 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0021 | 0/0 | 2882 | 2 | 0 | 0 | 1 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0022 | 0/0 | 2883 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0023 | 0/0 | 2881 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0024 | 0/0 | 2884 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0025 | 0/0 | 2881 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0026 | 0/0 | 2878 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0027 | 0/0 | 2881 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0028 | 0/0 | 2881 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0029 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0030 | 0/0 | 2883 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0031 | 1/0 | 2885 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0032 | 0/0 | 2882 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0033 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
t0034 | 0/0 | 2882 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 6 | 9 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0002 | 0/0 | 13 | 0 | 0 | 10 | 2 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0003 | 0/0 | 12 | 0 | 1 | 9 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0006 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0008 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0009 | 0/0 | 6 | 0 | 0 | 4 | 1 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0010 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0011 | 0/0 | 6 | 0 | 1 | 1 | 2 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0014 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0017 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0019 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0028 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 678 | 425 | 85 | 80 | 199 | 16 | 43 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0002 | 0/0 | 678 | 10 | 10 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0004 | 0/0 | 678 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0005 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0002c0003 | 0/0 | 678 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0003c0006 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3560 | 88 | 7 | 19 | 54 | 2 | 6 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0002 | 0/0 | 3563 | 84 | 15 | 5 | 60 | 0 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0003 | 0/0 | 3558 | 54 | 7 | 12 | 27 | 2 | 6 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0004 | 0/0 | 3559 | 46 | 24 | 9 | 4 | 2 | 7 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0005 | 0/0 | 3559 | 41 | 1 | 6 | 20 | 4 | 10 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0006 | 0/0 | 3562 | 15 | 12 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0007 | 0/0 | 3559 | 15 | 0 | 9 | 1 | 1 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0008 | 0/1 | 3562 | 9 | 2 | 6 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0009 | 0/0 | 3563 | 9 | 9 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0010 | 0/0 | 3558 | 7 | 0 | 1 | 6 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0011 | 0/0 | 3559 | 7 | 0 | 3 | 0 | 3 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0012 | 0/0 | 3560 | 6 | 2 | 1 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0013 | 0/0 | 3559 | 5 | 0 | 3 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0014 | 0/0 | 3561 | 4 | 1 | 2 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0015 | 0/0 | 3560 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0016 | 0/0 | 3559 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0017 | 0/0 | 3561 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0018 | 0/0 | 3560 | 4 | 0 | 0 | 3 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0019 | 0/0 | 3559 | 3 | 0 | 0 | 0 | 0 | 3 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0020 | 0/0 | 3556 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0021 | 0/0 | 3559 | 2 | 0 | 0 | 1 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0022 | 0/0 | 3560 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0023 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0024 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0025 | 0/0 | 3558 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0026 | 0/0 | 3555 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0027 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0028 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0029 | 0/0 | 3563 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0030 | 0/0 | 3560 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0031 | 1/0 | 3562 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0001t0033 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0002t0004 | 0/0 | 3559 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0002t0012 | 0/0 | 3560 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0002t0032 | 0/0 | 3559 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0002t0034 | 0/0 | 3559 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0004t0001 | 0/0 | 3560 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0001c0005t0016 | 0/0 | 3559 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0002c0003t0003 | 0/0 | 3558 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
a0003c0006t0001 | 0/0 | 3605 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | copy fasta | chr2 | 118083471 | 118115997 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 0 | 6 | 9 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 4 | 1 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0019 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0002 | 0/0 | 13 | 0 | 0 | 10 | 2 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0017 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0011 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0008 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0008g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0008g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0008g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0008g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0008g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0010g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0010g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0010g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0011g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0011g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0011g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0011g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0011g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0012g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0012g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0012g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0012g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0013g0014 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0014g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0014g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0014g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0014g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0015g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0016g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0017g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0017g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0017g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0017g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0018g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0018g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0018g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0018g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0019g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0019g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0020g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0020g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0020g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0021g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0021g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0022g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0023g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0024g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0025g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0026g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0027g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0028g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0029g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0030g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0031g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0001t0033g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0004g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0032g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0002t0034g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0004t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0001c0005t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0002c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0002c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
a0003c0006t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0045 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00099 | hp2 | a0001 | c0001 | t0013 | g0014 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00140 | hp1 | a0001 | c0001 | t0011 | g0181 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0104 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0011 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0011 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00323 | hp2 | a0001 | c0001 | t0011 | g0182 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00438 | hp2 | a0001 | c0001 | t0010 | g0142 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00544 | hp1 | a0001 | c0001 | t0012 | g0224 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00597 | hp1 | a0001 | c0001 | t0021 | g0119 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00639 | hp2 | a0001 | c0001 | t0030 | g0091 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00642 | hp2 | a0001 | c0001 | t0025 | g0123 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00738 | hp1 | a0001 | c0001 | t0013 | g0014 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00738 | hp2 | a0001 | c0001 | t0022 | g0054 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00741 | hp1 | a0001 | c0001 | t0022 | g0054 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0037 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0144 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0051 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0051 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0037 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01074 | hp1 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0249 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01168 | hp2 | a0001 | c0001 | t0012 | g0208 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01192 | hp1 | a0001 | c0001 | t0013 | g0014 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0100 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0026 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0198 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0253 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01261 | hp1 | a0001 | c0001 | t0014 | g0127 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0254 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01346 | hp2 | a0001 | c0001 | t0013 | g0014 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01361 | hp1 | a0001 | c0001 | t0011 | g0010 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01361 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01515 | hp1 | a0001 | c0001 | t0013 | g0014 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0049 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0049 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01891 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01934 | hp2 | a0001 | c0001 | t0007 | g0247 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01993 | hp1 | a0001 | c0001 | t0014 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02015 | hp2 | a0001 | c0001 | t0017 | g0222 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02129 | hp1 | a0001 | c0001 | t0010 | g0141 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02155 | hp1 | a0001 | c0001 | t0010 | g0018 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0032 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02273 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02572 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0189 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0109 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02630 | hp1 | a0001 | c0001 | t0024 | g0108 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0260 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0003 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0170 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0094 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02818 | hp1 | a0001 | c0001 | t0016 | g0161 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02886 | hp1 | a0001 | c0001 | t0016 | g0162 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02895 | hp1 | a0001 | c0001 | t0027 | g0269 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0166 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0237 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0238 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0240 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03130 | hp2 | a0001 | c0002 | t0012 | g0233 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0158 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0008 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0193 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0163 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0027 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03516 | hp2 | a0001 | c0002 | t0004 | g0257 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0156 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03579 | hp2 | a0001 | c0005 | t0016 | g0159 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0204 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0268 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0177 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03688 | hp2 | a0001 | c0001 | t0011 | g0176 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03704 | hp2 | a0001 | c0001 | t0021 | g0146 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0008 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03710 | hp2 | a0001 | c0001 | t0019 | g0039 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03831 | hp1 | a0001 | c0001 | t0018 | g0214 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03831 | hp2 | a0001 | c0001 | t0019 | g0039 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0098 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0192 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03942 | hp1 | a0001 | c0001 | t0019 | g0125 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0250 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0011 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18947 | hp2 | a0001 | c0001 | t0020 | g0006 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18954 | hp1 | a0001 | c0001 | t0017 | g0221 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18968 | hp2 | a0003 | c0006 | t0001 | g0197 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18969 | hp1 | a0001 | c0001 | t0012 | g0225 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18970 | hp1 | a0001 | c0001 | t0023 | g0018 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18978 | hp1 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18981 | hp1 | a0001 | c0001 | t0012 | g0218 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18982 | hp1 | a0001 | c0001 | t0026 | g0131 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18983 | hp1 | a0001 | c0001 | t0029 | g0035 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18984 | hp1 | a0001 | c0001 | t0018 | g0157 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18984 | hp2 | a0001 | c0001 | t0010 | g0018 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18991 | hp2 | a0001 | c0001 | t0017 | g0262 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18993 | hp2 | a0001 | c0001 | t0020 | g0164 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19004 | hp1 | a0001 | c0001 | t0028 | g0024 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19004 | hp2 | a0001 | c0001 | t0033 | g0061 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19005 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19006 | hp1 | a0001 | c0001 | t0014 | g0133 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19006 | hp2 | a0001 | c0001 | t0020 | g0011 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19030 | hp1 | a0001 | c0002 | t0004 | g0259 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19030 | hp2 | a0001 | c0002 | t0034 | g0256 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19054 | hp1 | a0001 | c0001 | t0018 | g0015 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19055 | hp1 | a0001 | c0001 | t0018 | g0205 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19055 | hp2 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19056 | hp1 | a0001 | c0001 | t0010 | g0018 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19056 | hp2 | a0002 | c0003 | t0003 | g0118 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19057 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19057 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19067 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19067 | hp2 | a0001 | c0001 | t0017 | g0210 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19072 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19082 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19086 | hp1 | a0001 | c0001 | t0010 | g0140 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19086 | hp2 | a0002 | c0003 | t0003 | g0117 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19087 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19089 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20129 | hp1 | a0001 | c0001 | t0012 | g0239 | AFR | ASW | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ASW | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20752 | hp1 | a0001 | c0001 | t0007 | g0252 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20805 | hp2 | a0001 | c0001 | t0011 | g0174 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | GIH | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0251 | SAS | GIH | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0093 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG03471 | hp2 | a0001 | c0002 | t0032 | g0147 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20300 | hp1 | a0001 | c0002 | t0004 | g0258 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0110 | REF | REF | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0031 | g0160 | REF | REF | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:118106800
|
T | TGGTGGAC others(38): Show |
1 | a0003 | 1 | NA18968.hp2 | disruptive_inframe_insertion | MODERATE | c.435_479dupGTGGACTT others(37): Show |
p.Gly160_Ile161insTr others(43): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 4/6 | 689/3562 | 480/678 | 160/225 | INFO_REALIGN_3_PRIME | chr2 | 118106800 | |
chr2:118108299
|
G | A | 1 | a0002 | 2 | NA19056.hp2 NA19086.hp2 |
missense_variant | MODERATE | c.655G>A | p.Ala219Thr | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 864/3562 | 655/678 | 219/225 | chr2 | 118108299 | ||
chr2:118110997
|
A | G | 1 | a0001 | 1 | HG02895.hp1 | splice_region_variant | LOW | c.*2675A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | chr2 | 118110997 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:118103297
|
T | C | 1 | a0001c0004 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.345T>C | p.Phe115Phe | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/6 | 554/3562 | 345/678 | 115/225 | chr2 | 118103297 | ||
chr2:118107180
|
A | G | 1 | a0001c0002 | 10 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
synonymous_variant | LOW | c.627A>G | p.Gln209Gln | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/6 | 836/3562 | 627/678 | 209/225 | chr2 | 118107180 | ||
chr2:118108307
|
A | G | 1 | a0001c0005 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.663A>G | p.Lys221Lys | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 872/3562 | 663/678 | 221/225 | chr2 | 118108307 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:118088485
|
G | A | 1 | a0001c0001t0019 | 3 | HG03710.hp2 HG03831.hp2 HG03942.hp1 |
5_prime_UTR_variant | MODIFIER | c.-195G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/6 | 8072 | chr2 | 118088485 | |||||
chr2:118096518
|
A | AT | 7 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(4): Show | 110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-26dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/6 | 25 | INFO_REALIGN_3_PRIME | chr2 | 118096518 | ||||
chr2:118096518
|
AT | A | 12 | a0001c0001t0003a0001c0001t0010a0001c0001t0014others(9): Show | 78 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-26delT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/6 | 26 | INFO_REALIGN_3_PRIME | chr2 | 118096518 | ||||
chr2:118108424
|
G | C | 2 | a0001c0001t0010a0001c0001t0023 | 8 | HG00438.hp2 HG01069.hp2 HG02129.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*102G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 102 | chr2 | 118108424 | |||||
chr2:118108457
|
G | GA | 9 | a0001c0001t0001a0001c0001t0015a0001c0001t0017others(6): Show | 105 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*136dupA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 137 | INFO_REALIGN_3_PRIME | chr2 | 118108457 | ||||
chr2:118108816
|
A | C | 1 | a0001c0001t0013 | 5 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*494A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 494 | chr2 | 118108816 | |||||
chr2:118108935
|
C | T | 1 | a0001c0002t0034 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 613 | chr2 | 118108935 | |||||
chr2:118108936
|
G | A | 3 | a0001c0001t0008a0001c0001t0009a0001c0001t0024 | 19 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*614G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 614 | chr2 | 118108936 | |||||
chr2:118109215
|
C | T | 1 | a0001c0001t0011 | 7 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 893 | chr2 | 118109215 | |||||
chr2:118109387
|
C | T | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | 439 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(436): Show |
3_prime_UTR_variant | MODIFIER | c.*1065C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 1065 | chr2 | 118109387 | |||||
chr2:118109660
|
C | G | 2 | a0001c0001t0016a0001c0005t0016 | 4 | HG02818.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1338C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 1338 | chr2 | 118109660 | |||||
chr2:118110437
|
TGAG | T | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(27): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*2132_*2134delAGG | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2132 | INFO_REALIGN_3_PRIME | chr2 | 118110437 | ||||
chr2:118110469
|
T | C | 6 | a0001c0001t0005a0001c0001t0018a0001c0001t0020others(3): Show | 51 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2147T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2147 | chr2 | 118110469 | |||||
chr2:118110626
|
T | C | 1 | a0001c0001t0030 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2304T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2304 | chr2 | 118110626 | |||||
chr2:118110654
|
T | C | 1 | a0001c0001t0015 | 4 | NA19005.hp2 NA19057.hp1 NA19072.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2332T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2332 | chr2 | 118110654 | |||||
chr2:118110682
|
A | G | 1 | a0001c0001t0028 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2360 | chr2 | 118110682 | |||||
chr2:118110730
|
T | C | 1 | a0001c0002t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2408T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2408 | chr2 | 118110730 | |||||
chr2:118110813
|
AAAC | A | 5 | a0001c0001t0007a0001c0001t0020a0001c0001t0022others(2): Show | 22 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2494_*2496delCAA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2494 | INFO_REALIGN_3_PRIME | chr2 | 118110813 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:118088569
|
C | G | 1 | a0001c0001t0027g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-139+28C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118088569 | ||||||
chr2:118088732
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-139+191C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118088732 | ||||||
chr2:118088881
|
G | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(40): Show | 84 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-139+340G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118088881 | ||||||
chr2:118089262
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-139+721A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089262 | ||||||
chr2:118089309
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-139+768T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089309 | ||||||
chr2:118089392
|
G | C | 1 | a0001c0001t0006g0093 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-139+851G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089392 | ||||||
chr2:118089394
|
T | G | 5 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(2): Show | 5 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139+853T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089394 | ||||||
chr2:118089446
|
G | A | 6 | a0001c0001t0009g0042a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 7 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-139+905G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089446 | ||||||
chr2:118089470
|
C | G | 7 | a0001c0001t0002g0033a0001c0001t0002g0261a0001c0001t0002g0263others(4): Show | 9 | HG00621.hp2 HG02027.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-139+929C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089470 | ||||||
chr2:118089530
|
A | G | 3 | a0001c0001t0004g0151a0001c0001t0006g0093a0001c0001t0006g0150 | 3 | HG03471.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-139+989A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089530 | ||||||
chr2:118089734
|
AAG | A | 5 | a0001c0002t0004g0032a0001c0002t0004g0257a0001c0002t0004g0258others(2): Show | 7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-139+1196_-139+119 others(6): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118089734 | |||||
chr2:118089760
|
A | G | 1 | a0001c0002t0034g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-139+1219A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089760 | ||||||
chr2:118089804
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-139+1263A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089804 | ||||||
chr2:118090113
|
G | C | 2 | a0001c0001t0002g0043a0001c0001t0018g0157 | 3 | NA18968.hp1 NA18984.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-139+1572G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090113 | ||||||
chr2:118090227
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(274): Show | 435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
intron_variant | MODIFIER | c.-139+1686A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090227 | ||||||
chr2:118090265
|
G | A | 62 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(59): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-139+1724G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090265 | ||||||
chr2:118090311
|
G | T | 1 | a0001c0001t0008g0051 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-139+1770G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090311 | ||||||
chr2:118090319
|
G | C | 70 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0015others(67): Show | 110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-139+1778G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090319 | ||||||
chr2:118090367
|
T | C | 5 | a0001c0002t0004g0032a0001c0002t0004g0257a0001c0002t0004g0258others(2): Show | 7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-139+1826T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090367 | ||||||
chr2:118090848
|
G | A | 2 | a0001c0001t0004g0099a0001c0001t0008g0100 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-139+2307G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090848 | ||||||
chr2:118090915
|
C | G | 1 | a0001c0001t0005g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-139+2374C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090915 | ||||||
chr2:118091248
|
G | A | 1 | a0001c0001t0018g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-139+2707G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091248 | ||||||
chr2:118091302
|
G | C | 1 | a0001c0001t0002g0052 | 2 | NA18972.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-139+2761G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091302 | ||||||
chr2:118091306
|
C | G | 2 | a0001c0001t0004g0099a0001c0001t0008g0100 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-139+2765C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091306 | ||||||
chr2:118091408
|
C | T | 1 | a0001c0002t0034g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-139+2867C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091408 | ||||||
chr2:118091437
|
G | C | 62 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(59): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-139+2896G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091437 | ||||||
chr2:118091542
|
T | G | 1 | a0001c0001t0002g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-139+3001T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091542 | ||||||
chr2:118091629
|
CTTTTA | C | 1 | a0001c0001t0001g0022 | 3 | HG01168.hp1 HG01169.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-139+3093_-139+309 others(9): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118091629 | |||||
chr2:118091663
|
T | A | 1 | a0001c0001t0002g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-139+3122T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091663 | ||||||
chr2:118091673
|
T | A | 1 | a0001c0001t0002g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-139+3132T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091673 | ||||||
chr2:118091782
|
A | G | 1 | a0001c0001t0004g0041 | 2 | HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-139+3241A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091782 | ||||||
chr2:118091854
|
A | G | 1 | a0001c0001t0006g0203 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-139+3313A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091854 | ||||||
chr2:118092176
|
G | A | 4 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0101others(1): Show | 4 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139+3635G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092176 | ||||||
chr2:118092274
|
A | G | 5 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(2): Show | 5 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139+3733A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092274 | ||||||
chr2:118092577
|
T | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0103a0001c0001t0014g0016 | 5 | HG01981.hp1 HG01993.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-3842T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092577 | ||||||
chr2:118092592
|
G | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0163 | 4 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-138-3827G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092592 | ||||||
chr2:118092643
|
A | G | 70 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0015others(67): Show | 110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-138-3776A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092643 | ||||||
chr2:118092811
|
TGATGAGG others(140): Show |
T | 8 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0101others(5): Show | 12 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-138-3605_-138-345 others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092811 | |||||
chr2:118092814
|
T | G | 2 | a0001c0001t0003g0107a0001c0001t0004g0041 | 3 | HG01192.hp2 HG01358.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-138-3605T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092814 | ||||||
chr2:118092859
|
A | AGAT | 3 | a0001c0001t0001g0092a0001c0001t0002g0060a0001c0001t0008g0026 | 6 | HG01255.hp1 HG02109.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-3536_-138-353 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092859 | |||||
chr2:118092880
|
T | G | 1 | a0001c0001t0020g0164 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-138-3539T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092880 | ||||||
chr2:118092883
|
T | G | 62 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(59): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-138-3536T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092883 | ||||||
chr2:118092889
|
CGAGGAGA others(65): Show |
C | 5 | a0001c0002t0004g0032a0001c0002t0004g0257a0001c0002t0004g0258others(2): Show | 7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-138-3484_-138-341 others(76): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092889 | |||||
chr2:118092893
|
G | A | 70 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0015others(67): Show | 110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-138-3526G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092893 | ||||||
chr2:118092933
|
A | G | 2 | a0001c0001t0004g0099a0001c0001t0008g0100 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-138-3486A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092933 | ||||||
chr2:118092946
|
T | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG00408.hp2 NA18951.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-138-3473T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092946 | ||||||
chr2:118092946
|
TGAGGAGG others(68): Show |
T | 1 | a0001c0001t0005g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-138-3427_-138-335 others(79): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092946 | |||||
chr2:118092949
|
G | T | 3 | a0001c0001t0008g0051a0001c0001t0030g0091a0001c0002t0032g0147 | 4 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-138-3470G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092949 | ||||||
chr2:118093003
|
A | AGAT | 60 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(57): Show | 91 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-138-3404_-138-340 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093003 | |||||
chr2:118093015
|
T | G | 13 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0101others(10): Show | 18 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-138-3404T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093015 | ||||||
chr2:118093015
|
TGAG | T | 60 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(57): Show | 91 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-138-3379_-138-337 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093015 | |||||
chr2:118093018
|
G | T | 10 | a0001c0001t0002g0007a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 17 | HG00621.hp2 HG00642.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.-138-3401G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093018 | ||||||
chr2:118093038
|
AGGAGAGT others(1343): Show |
A | 2 | a0001c0001t0002g0007a0001c0001t0002g0242 | 8 | HG02717.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-138-3352_-138-200 others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093038 | |||||
chr2:118093078
|
A | AGAT | 4 | a0001c0001t0005g0200a0001c0001t0006g0050a0001c0001t0006g0201others(1): Show | 5 | HG01884.hp2 HG02083.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-3317_-138-331 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093078 | |||||
chr2:118093078
|
AGATGATG others(2): Show |
A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-138-3323_-138-331 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093078 | |||||
chr2:118093106
|
G | A | 67 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(64): Show | 101 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-138-3313G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093106 | ||||||
chr2:118093120
|
C | A | 1 | a0001c0001t0004g0041 | 2 | HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-138-3299C>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093120 | ||||||
chr2:118093145
|
A | AGAT | 11 | a0001c0001t0005g0049a0001c0001t0009g0042a0001c0001t0009g0152others(8): Show | 13 | HG01515.hp2 HG01517.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-138-3253_-138-325 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093145 | |||||
chr2:118093209
|
A | AGAT | 4 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0006g0093others(1): Show | 5 | HG02040.hp2 HG02056.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-3172_-138-317 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | |||||
chr2:118093209
|
A | AGATGAT | 8 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(5): Show | 8 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-138-3175_-138-317 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | |||||
chr2:118093209
|
AGAT | A | 75 | a0001c0001t0001g0028a0001c0001t0003g0036a0001c0001t0003g0145others(72): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-138-3172_-138-317 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | |||||
chr2:118093209
|
AGATGAT | A | 19 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0248others(16): Show | 25 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-138-3175_-138-317 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | |||||
chr2:118093209
|
AGATGATG others(5): Show |
A | 2 | a0001c0001t0004g0099a0001c0001t0008g0100 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-138-3181_-138-317 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | |||||
chr2:118093209
|
AGATGATG others(11): Show |
A | 68 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(65): Show | 102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-3187_-138-317 others(22): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | |||||
chr2:118093239
|
T | A | 1 | a0001c0001t0002g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-138-3180T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093239 | ||||||
chr2:118093288
|
AGAT | A | 61 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0017others(58): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-138-3119_-138-311 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093288 | |||||
chr2:118093297
|
T | G | 6 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(3): Show | 6 | HG02083.hp2 NA18953.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-3122T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093297 | ||||||
chr2:118093297
|
T | TGAG | 2 | a0001c0001t0004g0041a0001c0002t0034g0256 | 3 | HG01192.hp2 HG01358.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-138-3120_-138-311 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093297 | |||||
chr2:118093300
|
T | G | 43 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0017others(40): Show | 66 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-138-3119T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093300 | ||||||
chr2:118093300
|
T | TGAG | 18 | a0001c0001t0001g0248a0001c0001t0004g0169a0001c0001t0004g0245others(15): Show | 24 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-138-3094_-138-309 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | |||||
chr2:118093300
|
T | TGAGGAG | 29 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(26): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-138-3097_-138-309 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | |||||
chr2:118093300
|
T | TGATGAG | 28 | a0001c0001t0005g0006a0001c0001t0005g0011a0001c0001t0005g0027others(25): Show | 47 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-138-3117_-138-311 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | |||||
chr2:118093300
|
TGAG | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(49): Show | 104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-138-3094_-138-309 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | |||||
chr2:118093300
|
TGAGGAG | T | 5 | a0001c0001t0004g0099a0001c0001t0008g0100a0001c0001t0009g0237others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-3097_-138-309 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | |||||
chr2:118093303
|
G | T | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | NA18975.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-138-3116G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093303 | ||||||
chr2:118093306
|
G | T | 3 | a0001c0002t0004g0032a0001c0002t0004g0259a0001c0002t0004g0260 | 5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-3113G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093306 | ||||||
chr2:118093319
|
GAGGAGGA others(66): Show |
G | 10 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(7): Show | 10 | HG02083.hp2 HG03471.hp1 HG03471.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-3094_-138-302 others(77): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093319 | |||||
chr2:118093353
|
AAAAGCAA others(62): Show |
A | 1 | a0001c0001t0003g0112 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-138-3062_-138-299 others(73): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093353 | |||||
chr2:118093363
|
AGAT | A | 153 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0001g0248others(150): Show | 226 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-138-3029_-138-302 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093363 | |||||
chr2:118093363
|
AGATGAT | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-138-3032_-138-302 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093363 | |||||
chr2:118093433
|
A | AGAT | 6 | a0001c0001t0004g0046a0001c0001t0004g0185a0001c0001t0004g0186others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2965_-138-296 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | |||||
chr2:118093433
|
AGATGATG others(63): Show |
A | 49 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0017others(46): Show | 75 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-138-2962_-138-289 others(74): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | |||||
chr2:118093433
|
AGATGATG others(69): Show |
A | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(43): Show | 94 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-138-2962_-138-288 others(80): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | |||||
chr2:118093433
|
AGATGATG others(72): Show |
A | 3 | a0001c0001t0001g0065a0001c0001t0004g0099a0001c0001t0008g0100 | 3 | HG01109.hp1 HG01243.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-138-2962_-138-288 others(83): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | |||||
chr2:118093433
|
AGATGATG others(75): Show |
A | 1 | a0001c0001t0001g0087 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-138-2963_-138-288 others(86): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | |||||
chr2:118093436
|
TGATGATG others(54): Show |
T | 3 | a0001c0001t0004g0105a0001c0001t0006g0106a0001c0001t0013g0014 | 7 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-138-2962_-138-290 others(65): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093436 | |||||
chr2:118093439
|
TGATGATG others(51): Show |
T | 9 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(6): Show | 11 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-138-2962_-138-290 others(62): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093439 | |||||
chr2:118093442
|
TGATGATG others(48): Show |
T | 1 | a0001c0001t0008g0026 | 3 | HG01255.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-138-2962_-138-290 others(59): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093442 | |||||
chr2:118093497
|
AGAT | A | 6 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(3): Show | 6 | HG02083.hp2 NA18953.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2884_-138-288 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | |||||
chr2:118093497
|
AGATGAT | A | 23 | a0001c0001t0001g0248a0001c0001t0003g0112a0001c0001t0004g0245others(20): Show | 31 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-138-2887_-138-288 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | |||||
chr2:118093497
|
AGATGATG others(5): Show |
A | 63 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(60): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-138-2893_-138-288 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | |||||
chr2:118093497
|
AGATGATG others(8): Show |
A | 68 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(65): Show | 102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-2896_-138-288 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | |||||
chr2:118093533
|
T | C | 1 | a0001c0001t0004g0245 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-138-2886T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093533 | ||||||
chr2:118093543
|
T | C | 77 | a0001c0001t0001g0028a0001c0001t0001g0248a0001c0001t0004g0010others(74): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-138-2876T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093543 | ||||||
chr2:118093576
|
AGATGAT | A | 13 | a0001c0001t0001g0248a0001c0001t0004g0245a0001c0001t0004g0246others(10): Show | 19 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-138-2831_-138-282 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093576 | |||||
chr2:118093588
|
T | G | 17 | a0001c0001t0001g0012a0001c0001t0001g0066a0001c0001t0003g0036others(14): Show | 26 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-138-2831T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093588 | ||||||
chr2:118093588
|
TGATGAG | T | 2 | a0001c0001t0004g0170a0001c0001t0005g0047 | 3 | HG02735.hp1 NA18946.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-138-2828_-138-282 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093588 | |||||
chr2:118093591
|
T | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(168): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-138-2828T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093591 | ||||||
chr2:118093591
|
T | TGAG | 67 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(64): Show | 101 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-138-2806_-138-280 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093591 | |||||
chr2:118093594
|
G | T | 3 | a0001c0001t0004g0099a0001c0001t0008g0026a0001c0001t0008g0100 | 5 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-2825G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093594 | ||||||
chr2:118093633
|
A | T | 1 | a0001c0001t0019g0039 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-138-2786A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093633 | ||||||
chr2:118093651
|
A | AGAT | 3 | a0001c0001t0004g0099a0001c0001t0008g0026a0001c0001t0008g0100 | 5 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-2756_-138-275 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093651 | |||||
chr2:118093651
|
AGAT | A | 65 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0062others(62): Show | 98 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-138-2756_-138-275 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093651 | |||||
chr2:118093660
|
T | TGAG | 39 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(36): Show | 85 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.-138-2757_-138-275 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093660 | |||||
chr2:118093660
|
T | TGAGGAG | 7 | a0001c0001t0001g0035a0001c0001t0004g0094a0001c0001t0004g0095others(4): Show | 7 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-138-2757_-138-275 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093660 | |||||
chr2:118093663
|
T | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 125 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.-138-2756T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093663 | ||||||
chr2:118093663
|
T | TGAG | 17 | a0001c0001t0001g0086a0001c0001t0003g0025a0001c0001t0003g0038others(14): Show | 22 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2731_-138-272 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | |||||
chr2:118093663
|
T | TGAGGAG | 6 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0081others(3): Show | 8 | HG02056.hp2 HG02257.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-138-2734_-138-272 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | |||||
chr2:118093663
|
T | TGATGATG others(8): Show |
1 | a0001c0001t0004g0243 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-138-2754_-138-275 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | |||||
chr2:118093663
|
TGAG | T | 11 | a0001c0001t0002g0261a0001c0001t0005g0190a0001c0001t0009g0042others(8): Show | 12 | HG00621.hp2 HG01891.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-138-2731_-138-272 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | |||||
chr2:118093663
|
TGAGGAG | T | 13 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(10): Show | 19 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-138-2734_-138-272 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | |||||
chr2:118093666
|
G | T | 2 | a0001c0001t0004g0268a0003c0006t0001g0197 | 2 | HG03669.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-138-2753G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093666 | ||||||
chr2:118093733
|
G | C | 2 | a0001c0001t0004g0099a0001c0001t0008g0100 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-138-2686G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093733 | ||||||
chr2:118093741
|
TGAA | T | 76 | a0001c0001t0001g0028a0001c0001t0001g0248a0001c0001t0004g0010others(73): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-138-2676_-138-267 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093741 | |||||
chr2:118093744
|
A | T | 1 | a0001c0001t0005g0244 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-138-2675A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093744 | ||||||
chr2:118093805
|
TGAA | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(113): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-138-2612_-138-261 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093805 | |||||
chr2:118093848
|
A | AGAT | 20 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0063others(17): Show | 26 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.-138-2556_-138-255 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093848 | |||||
chr2:118093848
|
AGAT | A | 67 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(64): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-138-2556_-138-255 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093848 | |||||
chr2:118093860
|
T | G | 1 | a0001c0001t0009g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-138-2559T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093860 | ||||||
chr2:118093863
|
T | G | 86 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(83): Show | 133 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-138-2556T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093863 | ||||||
chr2:118093863
|
T | TGAG | 8 | a0001c0001t0005g0244a0001c0001t0006g0111a0001c0001t0009g0042others(5): Show | 9 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-138-2534_-138-253 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093863 | |||||
chr2:118093863
|
TGAG | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0063others(4): Show | 8 | HG00099.hp1 HG01106.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-138-2534_-138-253 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093863 | |||||
chr2:118093866
|
G | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(99): Show | 173 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-138-2553G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093866 | ||||||
chr2:118093923
|
A | AGAT | 3 | a0001c0001t0004g0243a0001c0001t0007g0253a0001c0001t0007g0254 | 3 | HG01175.hp1 HG01257.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093923 | |||||
chr2:118093923
|
AGAT | A | 8 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0101others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093923 | |||||
chr2:118093923
|
AGATGAT | A | 8 | a0001c0001t0003g0017a0001c0001t0003g0023a0001c0001t0003g0113others(5): Show | 14 | HG00423.hp1 HG00597.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-138-2481_-138-247 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093923 | |||||
chr2:118093938
|
T | G | 1 | a0001c0001t0004g0104 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-138-2481T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093938 | ||||||
chr2:118093938
|
T | TGAGGAG | 3 | a0001c0001t0006g0111a0001c0001t0008g0037a0001c0001t0008g0110 | 4 | HG01069.hp1 HG01071.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138-2479_-138-247 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | |||||
chr2:118093938
|
TGATGAG | T | 80 | a0001c0001t0001g0028a0001c0001t0003g0002a0001c0001t0003g0016others(77): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | |||||
chr2:118093938
|
TGATGAGG others(2): Show |
T | 9 | a0001c0001t0004g0172a0001c0001t0006g0167a0001c0001t0006g0168others(6): Show | 11 | HG00438.hp2 HG01069.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | |||||
chr2:118093938
|
TGATGAGG others(5): Show |
T | 35 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(32): Show | 67 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-138-2478_-138-246 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | |||||
chr2:118093941
|
T | G | 11 | a0001c0001t0004g0041a0001c0001t0004g0104a0001c0001t0004g0171others(8): Show | 13 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-138-2478T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093941 | ||||||
chr2:118093941
|
T | TGAG | 21 | a0001c0001t0001g0248a0001c0001t0004g0095a0001c0001t0004g0096others(18): Show | 31 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-138-2447_-138-244 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | |||||
chr2:118093941
|
T | TGAGGAG | 6 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0101others(3): Show | 6 | HG01891.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2450_-138-244 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | |||||
chr2:118093941
|
TGAG | T | 7 | a0001c0001t0004g0046a0001c0001t0004g0187a0001c0001t0004g0188others(4): Show | 9 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-138-2447_-138-244 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | |||||
chr2:118093941
|
TGAGGAG | T | 13 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0232others(10): Show | 16 | HG01070.hp2 HG01071.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-138-2450_-138-244 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | |||||
chr2:118093941
|
TGAGGAGG others(2): Show |
T | 63 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(60): Show | 95 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-138-2453_-138-244 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | |||||
chr2:118093941
|
TGAGGAGG others(5): Show |
T | 14 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0035others(11): Show | 30 | HG00621.hp1 HG00639.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-138-2456_-138-244 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | |||||
chr2:118093944
|
G | T | 1 | a0001c0002t0034g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-138-2475G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093944 | ||||||
chr2:118093950
|
G | T | 5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0232others(2): Show | 7 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-138-2469G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093950 | ||||||
chr2:118093953
|
G | T | 68 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(65): Show | 102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-2466G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093953 | ||||||
chr2:118093956
|
G | GGAGAGTT others(207): Show |
1 | a0001c0001t0004g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2460_-138-245 others(218): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093956 | |||||
chr2:118093956
|
G | T | 68 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(65): Show | 102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-2463G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093956 | ||||||
chr2:118093959
|
G | T | 65 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(62): Show | 98 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-138-2460G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093959 | ||||||
chr2:118093962
|
G | T | 1 | a0001c0001t0002g0057 | 2 | NA18942.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-138-2457G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093962 | ||||||
chr2:118093967
|
A | AGAGTTCT others(353): Show |
1 | a0001c0001t0005g0027 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-138-2451_-138-245 others(364): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093967 | |||||
chr2:118093969
|
G | A | 1 | a0001c0001t0005g0027 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-138-2450G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093969 | ||||||
chr2:118094010
|
A | AGAT | 93 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0003g0002others(90): Show | 139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-138-2371_-138-236 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | |||||
chr2:118094010
|
A | AGATGAT | 27 | a0001c0001t0001g0028a0001c0001t0002g0015a0001c0001t0002g0020others(24): Show | 38 | HG00544.hp1 HG01257.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.-138-2374_-138-236 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | |||||
chr2:118094010
|
A | AGATGATG others(2): Show |
32 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0002g0033others(29): Show | 52 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-138-2377_-138-236 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | |||||
chr2:118094010
|
A | AGATGATG others(5): Show |
7 | a0001c0001t0002g0055a0001c0001t0002g0209a0001c0001t0002g0211others(4): Show | 9 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.-138-2380_-138-236 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | |||||
chr2:118094010
|
AGAT | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(65): Show | 124 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-138-2371_-138-236 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | |||||
chr2:118094010
|
AGATGAT | A | 4 | a0001c0001t0001g0090a0001c0001t0004g0184a0001c0001t0008g0051others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-2374_-138-236 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | |||||
chr2:118094013
|
T | TGATGATG others(353): Show |
1 | a0001c0001t0005g0027 | 2 | HG00735.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-138-2319_-138-231 others(364): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | |||||
chr2:118094013
|
T | TGATGATG others(347): Show |
1 | a0001c0001t0004g0045 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-138-2316_-138-231 others(358): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | |||||
chr2:118094013
|
T | TGATGATG others(353): Show |
1 | a0001c0001t0004g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-138-2316_-138-231 others(364): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | |||||
chr2:118094013
|
T | TGATGATG others(356): Show |
1 | a0001c0001t0004g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-138-2316_-138-231 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | |||||
chr2:118094025
|
T | G | 11 | a0001c0001t0004g0041a0001c0001t0004g0101a0001c0001t0004g0104others(8): Show | 19 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-138-2394T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094025 | ||||||
chr2:118094028
|
T | G | 14 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(11): Show | 22 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2391T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094028 | ||||||
chr2:118094031
|
T | G | 14 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(11): Show | 22 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2388T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094031 | ||||||
chr2:118094034
|
T | G | 14 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(11): Show | 22 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2385T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094034 | ||||||
chr2:118094037
|
T | G | 14 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(11): Show | 22 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2382T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094037 | ||||||
chr2:118094040
|
T | G | 14 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(11): Show | 22 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2379T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094040 | ||||||
chr2:118094043
|
T | G | 12 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(9): Show | 20 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-138-2376T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094043 | ||||||
chr2:118094045
|
ATGAT | A | 12 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(9): Show | 20 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-138-2373_-138-237 others(8): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094045 | ||||||
chr2:118094049
|
T | A | 1 | a0001c0001t0004g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2370T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094049 | ||||||
chr2:118094051
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-138-2368G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094051 | ||||||
chr2:118094078
|
T | C | 1 | a0001c0001t0004g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2341T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094078 | ||||||
chr2:118094079
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2340G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094079 | ||||||
chr2:118094089
|
AGAT | A | 4 | a0001c0001t0003g0025a0001c0001t0003g0107a0001c0001t0003g0145others(1): Show | 6 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2315_-138-231 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094089 | |||||
chr2:118094092
|
T | TGATGATG others(350): Show |
1 | a0001c0001t0005g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-138-2319_-138-231 others(361): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094092 | |||||
chr2:118094092
|
T | TGATGATG others(356): Show |
1 | a0001c0001t0005g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-138-2316_-138-231 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094092 | |||||
chr2:118094092
|
T | TGATGATG others(124): Show |
1 | a0001c0001t0004g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2313_-138-231 others(135): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094092 | |||||
chr2:118094101
|
T | G | 42 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0017others(39): Show | 64 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-138-2318T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094101 | ||||||
chr2:118094101
|
TGATGAGG others(2): Show |
T | 3 | a0001c0001t0004g0151a0001c0001t0006g0093a0001c0001t0006g0150 | 3 | HG03471.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-138-2315_-138-230 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094101 | |||||
chr2:118094101
|
TGATGAGG others(5): Show |
T | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(45): Show | 96 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.-138-2315_-138-230 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094101 | |||||
chr2:118094104
|
T | G | 132 | a0001c0001t0001g0028a0001c0001t0001g0248a0001c0001t0002g0019others(129): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-138-2315T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094104 | ||||||
chr2:118094104
|
T | TGAG | 3 | a0001c0001t0004g0171a0001c0001t0005g0163a0001c0001t0005g0204 | 3 | HG03491.hp1 HG03654.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-138-2293_-138-229 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094104 | |||||
chr2:118094104
|
TGAGGAG | T | 15 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(12): Show | 24 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-138-2296_-138-229 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094104 | |||||
chr2:118094107
|
G | T | 1 | a0001c0001t0002g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-138-2312G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094107 | ||||||
chr2:118094169
|
A | T | 1 | a0001c0001t0002g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-138-2250A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094169 | ||||||
chr2:118094179
|
T | G | 10 | a0001c0001t0001g0064a0001c0001t0002g0212a0001c0001t0002g0215others(7): Show | 10 | HG00609.hp1 HG01891.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-2240T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094179 | ||||||
chr2:118094182
|
G | T | 4 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0097others(1): Show | 4 | HG00642.hp1 HG02738.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138-2237G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094182 | ||||||
chr2:118094233
|
A | AGAT | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(162): Show | 276 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-138-2153_-138-215 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGAT | 33 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0143others(30): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-138-2156_-138-215 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(2): Show |
5 | a0001c0001t0001g0086a0001c0001t0004g0045a0001c0001t0004g0180others(2): Show | 6 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2159_-138-215 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(5): Show |
1 | a0001c0002t0034g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-138-2162_-138-215 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(356): Show |
1 | a0001c0001t0004g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(359): Show |
1 | a0001c0001t0004g0184 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(362): Show |
7 | a0001c0001t0004g0046a0001c0001t0004g0169a0001c0001t0004g0185others(4): Show | 7 | HG02451.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(373): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(362): Show |
1 | a0001c0001t0008g0051 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(373): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(359): Show |
1 | a0001c0001t0005g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(359): Show |
23 | a0001c0001t0005g0006a0001c0001t0005g0011a0001c0001t0005g0029others(20): Show | 37 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(359): Show |
1 | a0001c0001t0006g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(362): Show |
13 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(10): Show | 22 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(373): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(365): Show |
1 | a0001c0001t0004g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(376): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(365): Show |
2 | a0001c0001t0004g0178a0001c0001t0006g0202 | 2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(376): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | AGATGATG others(356): Show |
1 | a0001c0001t0005g0179 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094233
|
A | T | 1 | a0001c0001t0003g0116 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-138-2186A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094233 | ||||||
chr2:118094233
|
AGATGATG others(2): Show |
A | 1 | a0001c0001t0008g0026 | 3 | HG01255.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-138-2159_-138-215 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | |||||
chr2:118094269
|
A | T | 1 | a0001c0001t0003g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-138-2150A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094269 | ||||||
chr2:118094278
|
C | A | 1 | a0001c0001t0008g0026 | 3 | HG01255.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-138-2141C>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094278 | ||||||
chr2:118094315
|
TGATGATG others(45): Show |
T | 5 | a0001c0001t0001g0013a0001c0001t0001g0069a0001c0001t0001g0077others(2): Show | 9 | NA18942.hp1 NA18951.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-138-2092_-138-204 others(56): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094315 | |||||
chr2:118094367
|
A | AGATGATG others(5): Show |
186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 303 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.-138-2041_-138-203 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | |||||
chr2:118094367
|
A | AGATGATG others(8): Show |
68 | a0001c0001t0001g0028a0001c0001t0001g0070a0001c0001t0001g0080others(65): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-138-2044_-138-203 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | |||||
chr2:118094367
|
A | AGATGATG others(11): Show |
6 | a0001c0001t0002g0241a0001c0001t0003g0036a0001c0001t0004g0036others(3): Show | 6 | HG01891.hp1 HG01975.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-138-2047_-138-203 others(22): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | |||||
chr2:118094367
|
A | AGATGATG others(17): Show |
3 | a0001c0002t0004g0032a0001c0002t0004g0259a0001c0002t0004g0260 | 5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-2030_-138-202 others(28): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | |||||
chr2:118094367
|
A | AGATGATG others(20): Show |
1 | a0001c0002t0004g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-138-2030_-138-202 others(31): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | |||||
chr2:118094367
|
A | AGATGATG others(368): Show |
2 | a0001c0001t0005g0047a0001c0001t0006g0203 | 3 | NA18946.hp2 NA18971.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-138-2030_-138-202 others(379): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | |||||
chr2:118094367
|
A | AGATGATG others(8): Show |
1 | a0001c0001t0004g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-138-2039_-138-203 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | |||||
chr2:118094871
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-138-1548C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094871 | ||||||
chr2:118094971
|
C | G | 1 | a0001c0001t0002g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-138-1448C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094971 | ||||||
chr2:118095253
|
G | A | 1 | a0001c0001t0002g0230 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-138-1166G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118095253 | ||||||
chr2:118095278
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0004g0040 | 9 | HG02145.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-138-1141C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118095278 | ||||||
chr2:118096228
|
C | T | 2 | a0001c0001t0008g0037a0001c0001t0008g0110 | 3 | HG01069.hp1 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-138-191C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118096228 | ||||||
chr2:118096229
|
G | A | 1 | a0001c0002t0034g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-138-190G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118096229 | ||||||
chr2:118096271
|
T | C | 1 | a0001c0001t0002g0060 | 2 | NA18948.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-138-148T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118096271 | ||||||
chr2:118096935
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.244+135C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118096935 | ||||||
chr2:118096936
|
G | C | 1 | a0001c0001t0002g0232 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.244+136G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118096936 | ||||||
chr2:118097137
|
A | G | 2 | a0001c0002t0004g0257a0001c0002t0004g0258 | 2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.244+337A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097137 | ||||||
chr2:118097150
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0004g0040 | 9 | HG02145.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+350C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097150 | ||||||
chr2:118097172
|
A | AT | 276 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(273): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.244+374dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118097172 | |||||
chr2:118097348
|
G | A | 62 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(59): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.244+548G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097348 | ||||||
chr2:118097365
|
C | T | 3 | a0001c0001t0002g0056a0001c0001t0017g0210a0001c0001t0017g0221 | 4 | NA18954.hp1 NA18969.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+565C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097365 | ||||||
chr2:118097633
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.244+833T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097633 | ||||||
chr2:118097867
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.244+1067G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097867 | ||||||
chr2:118098231
|
C | T | 15 | a0001c0001t0001g0248a0001c0001t0004g0245a0001c0001t0004g0246others(12): Show | 21 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.244+1431C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098231 | ||||||
chr2:118098351
|
G | A | 62 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(59): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.244+1551G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098351 | ||||||
chr2:118098580
|
G | A | 7 | a0001c0001t0001g0248a0001c0001t0007g0008a0001c0001t0007g0247others(4): Show | 13 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+1780G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098580 | ||||||
chr2:118098728
|
C | T | 1 | a0001c0001t0005g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.244+1928C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098728 | ||||||
chr2:118098891
|
A | G | 1 | a0001c0001t0014g0133 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.244+2091A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098891 | ||||||
chr2:118099007
|
T | C | 3 | a0001c0002t0004g0032a0001c0002t0004g0259a0001c0002t0004g0260 | 5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+2207T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099007 | ||||||
chr2:118099035
|
A | G | 6 | a0001c0001t0003g0132a0001c0002t0004g0032a0001c0002t0004g0257others(3): Show | 8 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+2235A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099035 | ||||||
chr2:118099191
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.244+2391G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099191 | ||||||
chr2:118099338
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.244+2538A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099338 | ||||||
chr2:118099492
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.244+2692T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099492 | ||||||
chr2:118099618
|
A | G | 1 | a0001c0001t0004g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.244+2818A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099618 | ||||||
chr2:118099705
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.244+2905G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099705 | ||||||
chr2:118099712
|
C | G | 11 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0041others(8): Show | 17 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.244+2912C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099712 | ||||||
chr2:118099784
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.244+2984G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099784 | ||||||
chr2:118099950
|
C | T | 61 | a0001c0001t0001g0028a0001c0001t0004g0010a0001c0001t0004g0044others(58): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.244+3150C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099950 | ||||||
chr2:118100007
|
G | A | 3 | a0001c0002t0004g0032a0001c0002t0004g0259a0001c0002t0004g0260 | 5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-3190G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100007 | ||||||
chr2:118100019
|
T | C | 1 | a0001c0001t0003g0038 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.245-3178T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100019 | ||||||
chr2:118100073
|
T | A | 4 | a0001c0001t0003g0025a0001c0001t0003g0107a0001c0001t0003g0145others(1): Show | 6 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-3124T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100073 | ||||||
chr2:118100130
|
A | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(273): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.245-3067A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100130 | ||||||
chr2:118100172
|
G | A | 1 | a0001c0001t0021g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.245-3025G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100172 | ||||||
chr2:118100175
|
A | C | 2 | a0001c0001t0012g0239a0001c0001t0012g0240 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3022A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100175 | ||||||
chr2:118100184
|
T | C | 2 | a0001c0001t0012g0239a0001c0001t0012g0240 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3013T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100184 | ||||||
chr2:118100185
|
G | C | 2 | a0001c0001t0012g0239a0001c0001t0012g0240 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3012G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100185 | ||||||
chr2:118100186
|
A | T | 2 | a0001c0001t0012g0239a0001c0001t0012g0240 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3011A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100186 | ||||||
chr2:118100187
|
A | C | 2 | a0001c0001t0012g0239a0001c0001t0012g0240 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3010A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100187 | ||||||
chr2:118100217
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.245-2980G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100217 | ||||||
chr2:118100373
|
C | CT | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.245-2801dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | |||||
chr2:118100373
|
C | CTT | 45 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0021others(42): Show | 65 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.245-2802_245-2801d others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | |||||
chr2:118100373
|
C | CTTT | 6 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0004g0245others(3): Show | 6 | HG00438.hp1 HG00438.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-2803_245-2801d others(5): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | |||||
chr2:118100373
|
CT | C | 56 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0015others(53): Show | 92 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.245-2801delT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | |||||
chr2:118100373
|
CTT | C | 8 | a0001c0001t0002g0019a0001c0001t0002g0209a0001c0001t0002g0213others(5): Show | 12 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.245-2802_245-2801d others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | |||||
chr2:118100415
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.245-2782G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100415 | ||||||
chr2:118100448
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.245-2749G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100448 | ||||||
chr2:118100488
|
C | A | 1 | a0001c0001t0004g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.245-2709C>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100488 | ||||||
chr2:118100495
|
C | G | 1 | a0001c0002t0034g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-2702C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100495 | ||||||
chr2:118100519
|
C | T | 5 | a0001c0002t0004g0032a0001c0002t0004g0257a0001c0002t0004g0258others(2): Show | 7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-2678C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100519 | ||||||
chr2:118100966
|
ATAACT | A | 8 | a0001c0001t0004g0046a0001c0001t0004g0169a0001c0001t0004g0184others(5): Show | 8 | HG02451.hp1 HG02486.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-2227_245-2223d others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100966 | |||||
chr2:118100977
|
G | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0236a0001c0001t0012g0224 | 6 | HG00544.hp1 NA18961.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-2220G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100977 | ||||||
chr2:118101192
|
A | G | 1 | a0001c0001t0005g0244 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.245-2005A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101192 | ||||||
chr2:118101248
|
C | T | 1 | a0001c0001t0003g0128 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.245-1949C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101248 | ||||||
chr2:118101460
|
G | T | 7 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0002g0052others(4): Show | 11 | NA18959.hp1 NA18968.hp1 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-1737G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101460 | ||||||
chr2:118101583
|
TG | T | 5 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(2): Show | 5 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1609delG | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118101583 | |||||
chr2:118101980
|
G | A | 12 | a0001c0001t0004g0040a0001c0001t0007g0008a0001c0001t0007g0061others(9): Show | 20 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.245-1217G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101980 | ||||||
chr2:118102066
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.245-1131G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102066 | ||||||
chr2:118102088
|
G | A | 1 | a0001c0001t0005g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.245-1109G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102088 | ||||||
chr2:118102137
|
G | C | 5 | a0001c0001t0004g0243a0001c0001t0016g0158a0001c0001t0016g0161others(2): Show | 5 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1060G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102137 | ||||||
chr2:118102550
|
T | C | 1 | a0001c0001t0005g0244 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.245-647T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102550 | ||||||
chr2:118102695
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0080 | 4 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-502G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102695 | ||||||
chr2:118102786
|
A | G | 2 | a0001c0001t0002g0263a0001c0001t0002g0265 | 2 | NA18981.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.245-411A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102786 | ||||||
chr2:118102851
|
G | A | 1 | a0001c0001t0017g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.245-346G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102851 | ||||||
chr2:118102879
|
GA | G | 12 | a0001c0001t0004g0046a0001c0001t0004g0166a0001c0001t0004g0169others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.245-316delA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118102879 | |||||
chr2:118102895
|
C | T | 119 | a0001c0001t0003g0036a0001c0001t0004g0010a0001c0001t0004g0036others(116): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.245-302C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102895 | ||||||
chr2:118102964
|
A | G | 2 | a0001c0002t0032g0147a0001c0002t0034g0256 | 2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.245-233A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102964 | ||||||
chr2:118102985
|
G | A | 11 | a0001c0001t0007g0008a0001c0001t0007g0061a0001c0001t0007g0247others(8): Show | 18 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.245-212G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102985 | ||||||
chr2:118103080
|
G | GT | 8 | a0001c0001t0001g0075a0001c0001t0004g0243a0001c0001t0016g0158others(5): Show | 8 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-104dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118103080 | |||||
chr2:118103808
|
T | C | 1 | a0001c0002t0032g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.369+487T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118103808 | ||||||
chr2:118103859
|
A | G | 40 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(37): Show | 69 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.369+538A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118103859 | ||||||
chr2:118104170
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.369+849G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104170 | ||||||
chr2:118104389
|
G | T | 5 | a0001c0001t0004g0243a0001c0001t0016g0158a0001c0001t0016g0161others(2): Show | 5 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+1068G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104389 | ||||||
chr2:118104517
|
A | T | 2 | a0001c0001t0008g0037a0001c0001t0008g0110 | 3 | HG01069.hp1 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.369+1196A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104517 | ||||||
chr2:118104521
|
A | T | 13 | a0001c0001t0008g0026a0001c0001t0008g0051a0001c0001t0008g0100others(10): Show | 17 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+1200A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104521 | ||||||
chr2:118104557
|
A | G | 24 | a0001c0001t0003g0036a0001c0001t0003g0130a0001c0001t0004g0036others(21): Show | 36 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.369+1236A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104557 | ||||||
chr2:118104621
|
A | G | 3 | a0001c0001t0004g0245a0001c0001t0004g0246a0001c0001t0004g0255 | 3 | HG00438.hp1 HG00597.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.369+1300A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104621 | ||||||
chr2:118104690
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.369+1369A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104690 | ||||||
chr2:118104776
|
G | C | 7 | a0001c0002t0004g0032a0001c0002t0004g0257a0001c0002t0004g0258others(4): Show | 9 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+1455G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104776 | ||||||
chr2:118104780
|
G | A | 1 | a0001c0002t0034g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.369+1459G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104780 | ||||||
chr2:118104819
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.369+1498A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104819 | ||||||
chr2:118104888
|
T | G | 33 | a0001c0001t0004g0010a0001c0001t0004g0044a0001c0001t0004g0046others(30): Show | 39 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.369+1567T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104888 | ||||||
chr2:118104916
|
T | C | 26 | a0001c0001t0004g0040a0001c0001t0007g0008a0001c0001t0007g0061others(23): Show | 39 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.369+1595T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104916 | ||||||
chr2:118105036
|
T | G | 85 | a0001c0001t0003g0036a0001c0001t0004g0010a0001c0001t0004g0036others(82): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.370-1701T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105036 | ||||||
chr2:118105064
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.370-1673G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105064 | ||||||
chr2:118105109
|
T | C | 146 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0019others(143): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.370-1628T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105109 | ||||||
chr2:118105243
|
A | G | 2 | a0001c0001t0004g0171a0001c0001t0004g0172 | 2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.370-1494A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105243 | ||||||
chr2:118105323
|
G | A | 14 | a0001c0001t0008g0026a0001c0001t0008g0037a0001c0001t0008g0051others(11): Show | 19 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.370-1414G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105323 | ||||||
chr2:118105345
|
T | C | 1 | a0001c0001t0006g0074 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.370-1392T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105345 | ||||||
chr2:118105545
|
G | A | 1 | a0001c0001t0010g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.370-1192G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105545 | ||||||
chr2:118105564
|
A | G | 6 | a0001c0002t0004g0032a0001c0002t0004g0257a0001c0002t0004g0258others(3): Show | 8 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-1173A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105564 | ||||||
chr2:118105822
|
C | T | 2 | a0001c0001t0005g0191a0001c0001t0005g0194 | 2 | NA19057.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.370-915C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105822 | ||||||
chr2:118106100
|
G | C | 1 | a0001c0001t0004g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.370-637G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118106100 | ||||||
chr2:118106194
|
G | A | 32 | a0001c0001t0004g0010a0001c0001t0004g0044a0001c0001t0004g0046others(29): Show | 38 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.370-543G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118106194 | ||||||
chr2:118106298
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.370-439C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118106298 | ||||||
chr2:118107300
|
T | C | 1 | a0001c0001t0004g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.636+111T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107300 | ||||||
chr2:118107327
|
A | G | 1 | a0001c0001t0004g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.636+138A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107327 | ||||||
chr2:118107412
|
A | G | 2 | a0002c0003t0003g0117a0002c0003t0003g0118 | 2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.636+223A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107412 | ||||||
chr2:118107557
|
A | C | 1 | a0001c0001t0007g0247 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636+368A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107557 | ||||||
chr2:118107558
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.636+369C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107558 | ||||||
chr2:118107864
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.637-417G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107864 | ||||||
chr2:118107872
|
A | C | 6 | a0001c0001t0004g0041a0001c0001t0004g0045a0001c0001t0004g0173others(3): Show | 8 | HG00099.hp1 HG01106.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-409A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107872 | ||||||
chr2:118107947
|
T | C | 1 | a0001c0001t0003g0121 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.637-334T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107947 | ||||||
chr2:118107981
|
C | T | 7 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0101others(4): Show | 11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-300C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107981 | ||||||
chr2:118108052
|
C | T | 5 | a0001c0001t0004g0243a0001c0001t0016g0158a0001c0001t0016g0161others(2): Show | 5 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-229C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108052 | ||||||
chr2:118108086
|
C | T | 7 | a0001c0001t0003g0036a0001c0001t0004g0036a0001c0001t0004g0101others(4): Show | 11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-195C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108086 | ||||||
chr2:118108093
|
G | A | 40 | a0001c0001t0004g0010a0001c0001t0004g0044a0001c0001t0004g0046others(37): Show | 48 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.637-188G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108093 | ||||||
chr2:118108179
|
TA | T | 4 | a0001c0001t0003g0017a0001c0001t0003g0124a0001c0001t0003g0129others(1): Show | 7 | HG00735.hp1 HG01167.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-101delA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108179 | ||||||
chr2:118108238
|
G | A | 14 | a0001c0001t0008g0026a0001c0001t0008g0037a0001c0001t0008g0051others(11): Show | 19 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-43G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108238 |