geneid | 2799 |
---|---|
ensemblid | ENSG00000135677.11 |
hgncid | 4422 |
symbol | GNS |
name | glucosamine (N-acetyl)-6-sulfatase |
refseq_nuc | NM_002076.4 |
refseq_prot | NP_002067.1 |
ensembl_nuc | ENST00000258145.8 |
ensembl_prot | ENSP00000258145.3 |
mane_status | MANE Select |
chr | chr12 |
start | 64713449 |
end | 64759406 |
strand | - |
ver | v1.2 |
region | chr12:64713449-64759406 |
region5000 | chr12:64708449-64764406 |
regionname0 | GNS_chr12_64713449_64759406 |
regionname5000 | GNS_chr12_64708449_64764406 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 552 | 343 | 85 | 63 | 137 | 14 | 42 | 93 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0002 | 0/0 | 552 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0003 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0004 | 0/0 | 552 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1659 | 243 | 67 | 37 | 101 | 9 | 28 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
c0002 | 1/0 | 1659 | 75 | 6 | 14 | 36 | 5 | 13 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
c0003 | 0/0 | 1659 | 13 | 0 | 12 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
c0004 | 0/0 | 1659 | 10 | 10 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
c0005 | 0/0 | 1659 | 7 | 7 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
c0006 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
c0007 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
c0008 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3423 | 152 | 26 | 21 | 80 | 6 | 18 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0002 | 1/0 | 3423 | 75 | 3 | 24 | 33 | 5 | 9 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0003 | 0/0 | 3423 | 54 | 3 | 11 | 22 | 3 | 15 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0004 | 0/0 | 3423 | 21 | 19 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0005 | 0/0 | 3426 | 10 | 10 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0006 | 0/0 | 3423 | 8 | 8 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0007 | 0/0 | 3423 | 6 | 6 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0008 | 0/0 | 3423 | 4 | 1 | 3 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0009 | 0/0 | 3423 | 3 | 3 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0010 | 0/0 | 3423 | 3 | 3 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0011 | 0/0 | 3425 | 3 | 3 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0012 | 0/0 | 3423 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0013 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0014 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0015 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0016 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0017 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0018 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0019 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0020 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
t0021 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0003 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0016 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1659 | 243 | 67 | 37 | 101 | 9 | 28 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002 | 1/0 | 1659 | 75 | 6 | 14 | 36 | 5 | 13 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0003 | 0/0 | 1659 | 13 | 0 | 12 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0004 | 0/0 | 1659 | 10 | 10 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0006 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0002c0005 | 0/0 | 1659 | 7 | 7 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0003c0008 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0004c0007 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5081 | 146 | 24 | 21 | 80 | 6 | 14 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0003 | 0/0 | 5081 | 52 | 3 | 11 | 21 | 3 | 14 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0004 | 0/0 | 5081 | 13 | 11 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0006 | 0/0 | 5081 | 8 | 8 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0007 | 0/0 | 5081 | 6 | 6 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0008 | 0/0 | 5081 | 4 | 1 | 3 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0009 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0010 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0011 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0013 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0014 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0015 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0016 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0001t0021 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0001 | 0/0 | 5081 | 6 | 2 | 0 | 0 | 0 | 4 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0002 | 1/0 | 5081 | 62 | 3 | 12 | 33 | 5 | 8 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0003 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0004 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0012 | 0/0 | 5081 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0017 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0018 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0002t0020 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0003t0002 | 0/0 | 5081 | 13 | 0 | 12 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0004t0005 | 0/0 | 5084 | 10 | 10 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0001c0006t0011 | 0/0 | 5083 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0002c0005t0004 | 0/0 | 5081 | 7 | 7 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0003c0008t0003 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
a0004c0007t0019 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | copy fasta | chr12 | 64708449 | 64764406 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0003 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0016 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0008g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0008g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0015g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0001t0021g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0017g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0018g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0002t0020g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0004t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0006t0011g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0001c0006t0011g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0002c0005t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0002c0005t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0002c0005t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0002c0005t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0002c0005t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0002c0005t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0002c0005t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0003c0008t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
a0004c0007t0019g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0002 | g0068 | EUR | GBR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0197 | EUR | GBR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0080 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00423 | hp2 | a0001 | c0002 | t0012 | g0083 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0056 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0130 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00733 | hp2 | a0001 | c0003 | t0002 | g0089 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00738 | hp1 | a0001 | c0003 | t0002 | g0031 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01070 | hp1 | a0001 | c0003 | t0002 | g0077 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0029 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0129 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0055 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01175 | hp2 | a0001 | c0002 | t0020 | g0074 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0034 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01258 | hp2 | a0001 | c0003 | t0002 | g0033 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01261 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01346 | hp2 | a0001 | c0003 | t0002 | g0054 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01361 | hp1 | a0004 | c0007 | t0019 | g0064 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01361 | hp2 | a0001 | c0002 | t0017 | g0093 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0321 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01433 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0060 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0146 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0098 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01891 | hp2 | a0001 | c0004 | t0005 | g0123 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0328 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02055 | hp2 | a0002 | c0005 | t0004 | g0101 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02132 | hp2 | a0001 | c0002 | t0012 | g0085 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02145 | hp1 | a0002 | c0005 | t0004 | g0100 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02280 | hp2 | a0001 | c0004 | t0005 | g0126 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0131 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02451 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0106 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02630 | hp2 | a0001 | c0001 | t0013 | g0138 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0329 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0140 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0078 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02886 | hp2 | a0002 | c0005 | t0004 | g0110 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0137 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0065 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02897 | hp1 | a0001 | c0001 | t0014 | g0066 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03041 | hp1 | a0001 | c0004 | t0005 | g0120 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03041 | hp2 | a0001 | c0006 | t0011 | g0332 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0135 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03098 | hp2 | a0002 | c0005 | t0004 | g0102 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0187 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03195 | hp1 | a0001 | c0004 | t0005 | g0119 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0188 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03225 | hp1 | a0001 | c0001 | t0021 | g0330 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03225 | hp2 | a0001 | c0004 | t0005 | g0292 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03239 | hp1 | a0001 | c0003 | t0002 | g0090 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0309 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03453 | hp1 | a0001 | c0004 | t0005 | g0125 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03453 | hp2 | a0002 | c0005 | t0004 | g0111 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03486 | hp1 | a0001 | c0004 | t0005 | g0121 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0301 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03579 | hp2 | a0002 | c0005 | t0004 | g0063 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0087 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0302 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0025 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0058 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18906 | hp2 | a0001 | c0004 | t0005 | g0124 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18962 | hp2 | a0003 | c0008 | t0003 | g0318 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18969 | hp2 | a0001 | c0002 | t0018 | g0081 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0289 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19240 | hp1 | a0001 | c0001 | t0016 | g0017 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0290 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20129 | hp2 | a0001 | c0004 | t0005 | g0122 | AFR | ASW | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0244 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0320 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0314 | SAS | GIH | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0075 | SAS | GIH | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01123 | hp1 | a0001 | c0003 | t0002 | g0067 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02109 | hp2 | a0001 | c0004 | t0005 | g0127 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02559 | hp1 | a0001 | c0006 | t0011 | g0333 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG02559 | hp2 | a0002 | c0005 | t0004 | g0109 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
NA21309 | hp2 | a0001 | c0002 | t0004 | g0051 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0258 | REF | REF | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0086 | REF | REF | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:64716802
|
C | T | 1 | a0002 | 7 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
missense_variant | MODERATE | c.1598G>A | p.Arg533His | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1728/5081 | 1598/1659 | 533/552 | chr12 | 64716802 | ||
chr12:64720149
|
G | C | 1 | a0004 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1453C>G | p.Pro485Ala | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/14 | 1583/5081 | 1453/1659 | 485/552 | chr12 | 64720149 | ||
chr12:64745666
|
T | C | 1 | a0003 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.518A>G | p.Tyr173Cys | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/14 | 648/5081 | 518/1659 | 173/552 | chr12 | 64745666 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:64716750
|
A | G | 1 | a0001c0004 | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.1650T>C | p.His550His | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1780/5081 | 1650/1659 | 550/552 | chr12 | 64716750 | ||
chr12:64744875
|
C | T | 1 | a0004c0007 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.558G>A | p.Leu186Leu | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/14 | 688/5081 | 558/1659 | 186/552 | chr12 | 64744875 | ||
chr12:64747808
|
C | T | 1 | a0001c0003 | 13 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(10): Show |
synonymous_variant | LOW | c.363G>A | p.Lys121Lys | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/14 | 493/5081 | 363/1659 | 121/552 | chr12 | 64747808 | ||
chr12:64752752
|
C | T | 6 | a0001c0001a0001c0004a0001c0006others(3): Show | 264 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(261): Show |
synonymous_variant | LOW | c.198G>A | p.Pro66Pro | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/14 | 328/5081 | 198/1659 | 66/552 | chr12 | 64752752 | ||
chr12:64759256
|
G | C | 1 | a0001c0006 | 2 | HG02559.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.21C>G | p.Ala7Ala | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/14 | 151/5081 | 21/1659 | 7/552 | chr12 | 64759256 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:64713671
|
T | TAA | 3 | a0001c0001t0011a0001c0004t0005a0001c0006t0011 | 13 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3068_*3069dupTT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 3069 | chr12 | 64713671 | |||||
chr12:64713900
|
G | C | 1 | a0001c0001t0014 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2841C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2841 | chr12 | 64713900 | |||||
chr12:64713932
|
C | T | 2 | a0001c0001t0021a0004c0007t0019 | 2 | HG01361.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2809G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2809 | chr12 | 64713932 | |||||
chr12:64714117
|
G | A | 1 | a0001c0001t0016 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2624C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2624 | chr12 | 64714117 | |||||
chr12:64714129
|
C | CA | 1 | a0001c0004t0005 | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2611dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2611 | chr12 | 64714129 | |||||
chr12:64714380
|
G | C | 6 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(3): Show | 209 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2361 | chr12 | 64714380 | |||||
chr12:64714751
|
T | C | 4 | a0001c0001t0006a0001c0001t0009a0001c0001t0013others(1): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1990A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1990 | chr12 | 64714751 | |||||
chr12:64714858
|
A | C | 1 | a0001c0002t0018 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1883T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1883 | chr12 | 64714858 | |||||
chr12:64715093
|
G | A | 1 | a0001c0001t0007 | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1648 | chr12 | 64715093 | |||||
chr12:64715285
|
G | A | 3 | a0001c0001t0007a0001c0001t0011a0001c0006t0011 | 9 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1456C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1456 | chr12 | 64715285 | |||||
chr12:64715388
|
C | T | 5 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(2): Show | 206 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1353G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1353 | chr12 | 64715388 | |||||
chr12:64715513
|
G | A | 1 | a0001c0001t0007 | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1228C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1228 | chr12 | 64715513 | |||||
chr12:64715799
|
T | C | 7 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(4): Show | 25 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*942A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 942 | chr12 | 64715799 | |||||
chr12:64715882
|
C | T | 1 | a0001c0002t0017 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*859G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 859 | chr12 | 64715882 | |||||
chr12:64715927
|
A | G | 1 | a0001c0001t0007 | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*814T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 814 | chr12 | 64715927 | |||||
chr12:64716088
|
T | G | 1 | a0001c0001t0013 | 2 | HG02630.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*653A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 653 | chr12 | 64716088 | |||||
chr12:64716175
|
T | C | 4 | a0001c0001t0006a0001c0001t0009a0001c0001t0013others(1): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*566A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 566 | chr12 | 64716175 | |||||
chr12:64716330
|
C | T | 7 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(4): Show | 25 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*411G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 411 | chr12 | 64716330 | |||||
chr12:64716361
|
G | A | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 246 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*380C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 380 | chr12 | 64716361 | |||||
chr12:64716472
|
G | A | 4 | a0001c0001t0003a0001c0002t0003a0001c0002t0020others(1): Show | 55 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*269C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 269 | chr12 | 64716472 | |||||
chr12:64716500
|
G | A | 1 | a0001c0001t0021 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 241 | chr12 | 64716500 | |||||
chr12:64716580
|
C | T | 2 | a0001c0001t0009a0001c0002t0012 | 5 | HG00423.hp2 HG01884.hp1 HG02132.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 161 | chr12 | 64716580 | |||||
chr12:64716682
|
C | T | 1 | a0001c0001t0015 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 59 | chr12 | 64716682 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:64716903
|
G | C | 19 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(16): Show | 19 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.1581-84C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64716903 | ||||||
chr12:64716972
|
C | T | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1581-153G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64716972 | ||||||
chr12:64716975
|
C | G | 4 | a0001c0001t0003g0298a0001c0001t0003g0310a0001c0001t0003g0319others(1): Show | 4 | NA18962.hp2 NA18969.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1581-156G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64716975 | ||||||
chr12:64717028
|
G | A | 24 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(21): Show | 25 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1581-209C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717028 | ||||||
chr12:64717114
|
G | T | 1 | a0001c0004t0005g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1581-295C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717114 | ||||||
chr12:64717249
|
T | C | 3 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145 | 3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1581-430A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717249 | ||||||
chr12:64717511
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1581-692G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717511 | ||||||
chr12:64717518
|
A | AT | 27 | a0001c0001t0004g0113a0001c0001t0004g0144a0001c0001t0006g0132others(24): Show | 28 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1581-700dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717518 | ||||||
chr12:64717518
|
AT | A | 8 | a0001c0001t0004g0099a0001c0001t0004g0104a0001c0001t0004g0105others(5): Show | 8 | HG01081.hp2 HG01109.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1581-700delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717518 | ||||||
chr12:64717518
|
ATTTTTTT others(1): Show |
A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(188): Show | 205 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1581-707_1581-700d others(10): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717518 | ||||||
chr12:64717563
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG00621.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1581-744T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717563 | ||||||
chr12:64717697
|
A | C | 1 | a0001c0001t0003g0297 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1581-878T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717697 | ||||||
chr12:64717799
|
G | A | 5 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581-980C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717799 | ||||||
chr12:64717825
|
T | A | 3 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145 | 3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1581-1006A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717825 | ||||||
chr12:64717918
|
G | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1581-1099C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717918 | ||||||
chr12:64718146
|
C | CAACAGGC others(81): Show |
1 | a0001c0001t0004g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1581-1415_1581-132 others(92): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718146 | ||||||
chr12:64718240
|
G | A | 1 | a0001c0001t0003g0320 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1581-1421C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718240 | ||||||
chr12:64718319
|
T | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(253): Show | 272 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1581-1500A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718319 | ||||||
chr12:64718788
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1580+1234C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718788 | ||||||
chr12:64718856
|
C | G | 3 | a0001c0002t0002g0022a0001c0002t0002g0026a0001c0002t0002g0071 | 3 | NA18943.hp1 NA18953.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1580+1166G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718856 | ||||||
chr12:64718894
|
A | G | 1 | a0001c0001t0008g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1580+1128T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718894 | ||||||
chr12:64719046
|
G | C | 14 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580+976C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719046 | ||||||
chr12:64719383
|
G | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(278): Show | 298 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1580+639C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719383 | ||||||
chr12:64719516
|
A | G | 2 | a0001c0001t0003g0267a0001c0001t0003g0270 | 2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1580+506T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719516 | ||||||
chr12:64719699
|
G | A | 4 | a0001c0001t0003g0298a0001c0001t0003g0310a0001c0001t0003g0319others(1): Show | 4 | NA18962.hp2 NA18969.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580+323C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719699 | ||||||
chr12:64719809
|
G | A | 14 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580+213C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719809 | ||||||
chr12:64720285
|
TA | T | 18 | a0001c0001t0001g0287a0001c0001t0004g0007a0001c0001t0004g0099others(15): Show | 19 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1420-104delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720285 | ||||||
chr12:64720319
|
C | T | 1 | a0001c0002t0002g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1420-137G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720319 | ||||||
chr12:64720406
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1420-224A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720406 | ||||||
chr12:64720461
|
G | C | 1 | a0001c0001t0003g0317 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1420-279C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720461 | ||||||
chr12:64720855
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1420-673C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720855 | ||||||
chr12:64720866
|
C | G | 3 | a0001c0001t0003g0191a0001c0001t0003g0193a0001c0001t0003g0313 | 3 | HG01109.hp1 HG01255.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1420-684G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720866 | ||||||
chr12:64720875
|
TTA | T | 3 | a0001c0001t0008g0129a0001c0001t0008g0130a0001c0001t0008g0131 | 3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1420-695_1420-694d others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720875 | ||||||
chr12:64720983
|
T | G | 13 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0029others(10): Show | 13 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1419+612A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720983 | ||||||
chr12:64721020
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1419+575A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721020 | ||||||
chr12:64721150
|
T | A | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1419+445A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721150 | ||||||
chr12:64721215
|
C | G | 1 | a0001c0001t0003g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1419+380G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721215 | ||||||
chr12:64721322
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1419+273T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721322 | ||||||
chr12:64722008
|
TC | T | 14 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1309-304delG | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722008 | ||||||
chr12:64722064
|
G | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0158others(28): Show | 33 | HG00323.hp1 HG00408.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.1309-359C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722064 | ||||||
chr12:64722117
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1309-412G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722117 | ||||||
chr12:64722174
|
C | T | 1 | a0001c0001t0003g0316 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1309-469G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722174 | ||||||
chr12:64722327
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(224): Show | 242 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1309-622G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722327 | ||||||
chr12:64722532
|
A | G | 1 | a0001c0002t0018g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1308+474T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722532 | ||||||
chr12:64722624
|
C | T | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1308+382G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722624 | ||||||
chr12:64722667
|
C | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(222): Show | 240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1308+339G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722667 | ||||||
chr12:64722766
|
G | A | 1 | a0001c0002t0002g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1308+240C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722766 | ||||||
chr12:64722816
|
T | A | 1 | a0001c0001t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1308+190A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722816 | ||||||
chr12:64722817
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1308+189G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722817 | ||||||
chr12:64723218
|
C | G | 1 | a0001c0001t0004g0144 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1201-105G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723218 | ||||||
chr12:64723308
|
C | T | 14 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1201-195G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723308 | ||||||
chr12:64723561
|
A | G | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1201-448T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723561 | ||||||
chr12:64723609
|
T | C | 2 | a0001c0003t0002g0053a0001c0003t0002g0056 | 2 | HG00639.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1201-496A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723609 | ||||||
chr12:64723893
|
T | C | 3 | a0001c0001t0011g0106a0001c0006t0011g0332a0001c0006t0011g0333 | 3 | HG02559.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1201-780A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723893 | ||||||
chr12:64723943
|
C | T | 1 | a0001c0004t0005g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-830G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723943 | ||||||
chr12:64724373
|
T | C | 3 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0010g0289 | 3 | HG03139.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1201-1260A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724373 | ||||||
chr12:64724452
|
A | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0230a0001c0001t0001g0233others(2): Show | 5 | HG02015.hp2 HG02080.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-1339T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724452 | ||||||
chr12:64724487
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1201-1374G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724487 | ||||||
chr12:64724490
|
G | C | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1201-1377C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724490 | ||||||
chr12:64724501
|
A | G | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1201-1388T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724501 | ||||||
chr12:64724513
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1201-1400G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724513 | ||||||
chr12:64724523
|
C | T | 1 | a0001c0001t0007g0116 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1201-1410G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724523 | ||||||
chr12:64724543
|
C | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(127): Show | 138 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1201-1430G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724543 | ||||||
chr12:64724627
|
G | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-1514C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724627 | ||||||
chr12:64724667
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1201-1554C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724667 | ||||||
chr12:64725449
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1201-2336T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725449 | ||||||
chr12:64725928
|
G | A | 1 | a0001c0002t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1201-2815C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725928 | ||||||
chr12:64725995
|
C | CA | 17 | a0001c0001t0004g0144a0001c0001t0006g0118a0001c0001t0006g0132others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1201-2883dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725995 | ||||||
chr12:64725995
|
CA | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(193): Show | 210 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1201-2883delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725995 | ||||||
chr12:64725995
|
CAA | C | 17 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0208others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-2884_1201-288 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725995 | ||||||
chr12:64726204
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1200+2752C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726204 | ||||||
chr12:64726297
|
C | T | 10 | a0001c0004t0005g0119a0001c0004t0005g0120a0001c0004t0005g0121others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1200+2659G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726297 | ||||||
chr12:64726532
|
C | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(250): Show | 269 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1200+2424G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726532 | ||||||
chr12:64726578
|
T | G | 1 | a0001c0001t0003g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1200+2378A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726578 | ||||||
chr12:64726597
|
C | T | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1200+2359G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726597 | ||||||
chr12:64726928
|
T | TA | 15 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(12): Show | 15 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1200+2027dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726928 | ||||||
chr12:64726928
|
TA | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(220): Show | 238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1200+2027delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726928 | ||||||
chr12:64727119
|
T | C | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1200+1837A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727119 | ||||||
chr12:64727139
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1200+1817G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727139 | ||||||
chr12:64727212
|
T | C | 7 | a0002c0005t0004g0063a0002c0005t0004g0100a0002c0005t0004g0101others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+1744A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727212 | ||||||
chr12:64727270
|
T | TA | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(187): Show | 204 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1200+1685dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727270 | ||||||
chr12:64727367
|
CTGAGG | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(221): Show | 239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1200+1584_1200+158 others(9): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727367 | ||||||
chr12:64727373
|
C | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(221): Show | 239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1200+1583G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727373 | ||||||
chr12:64727375
|
GCAGT | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(221): Show | 239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1200+1577_1200+158 others(8): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727375 | ||||||
chr12:64727514
|
G | A | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1200+1442C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727514 | ||||||
chr12:64727584
|
G | A | 3 | a0001c0002t0002g0024a0001c0002t0002g0025a0001c0002t0002g0046 | 3 | HG03831.hp1 NA18956.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1200+1372C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727584 | ||||||
chr12:64727640
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(223): Show | 241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1200+1316C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727640 | ||||||
chr12:64727829
|
G | C | 7 | a0002c0005t0004g0063a0002c0005t0004g0100a0002c0005t0004g0101others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+1127C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727829 | ||||||
chr12:64728024
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1200+932T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728024 | ||||||
chr12:64728090
|
G | T | 1 | a0001c0004t0005g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1200+866C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728090 | ||||||
chr12:64728205
|
C | T | 1 | a0001c0004t0005g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+751G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728205 | ||||||
chr12:64728217
|
C | T | 1 | a0001c0002t0002g0024 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1200+739G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728217 | ||||||
chr12:64728383
|
T | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(250): Show | 269 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1200+573A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728383 | ||||||
chr12:64728415
|
T | C | 3 | a0001c0002t0002g0062a0001c0002t0012g0083a0001c0002t0012g0085 | 3 | HG00423.hp2 HG00558.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1200+541A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728415 | ||||||
chr12:64728491
|
T | C | 1 | a0001c0001t0003g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1200+465A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728491 | ||||||
chr12:64728516
|
G | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1200+440C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728516 | ||||||
chr12:64728556
|
G | C | 1 | a0001c0001t0006g0140 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1200+400C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728556 | ||||||
chr12:64728582
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0154a0001c0001t0001g0185 | 4 | HG02257.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+374C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728582 | ||||||
chr12:64728838
|
C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1200+118G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728838 | ||||||
chr12:64729185
|
T | A | 1 | a0001c0002t0002g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1099-128A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729185 | ||||||
chr12:64729197
|
T | A | 1 | a0001c0001t0003g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1099-140A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729197 | ||||||
chr12:64729356
|
T | C | 2 | a0001c0001t0003g0285a0001c0001t0003g0296 | 2 | HG00408.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.1099-299A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729356 | ||||||
chr12:64729478
|
A | G | 11 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0136others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-421T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729478 | ||||||
chr12:64729865
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1099-808A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729865 | ||||||
chr12:64730140
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1099-1083C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730140 | ||||||
chr12:64730230
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1099-1173A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730230 | ||||||
chr12:64730240
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(226): Show | 244 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1099-1183T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730240 | ||||||
chr12:64730309
|
C | T | 1 | a0001c0002t0002g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1099-1252G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730309 | ||||||
chr12:64730419
|
T | C | 1 | a0001c0001t0003g0312 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1099-1362A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730419 | ||||||
chr12:64730434
|
C | CA | 33 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0177others(30): Show | 33 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1099-1378dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730434 | ||||||
chr12:64730434
|
CA | C | 82 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0158others(79): Show | 88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1099-1378delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730434 | ||||||
chr12:64730434
|
CAA | C | 7 | a0001c0001t0003g0199a0001c0001t0003g0320a0001c0001t0003g0321others(4): Show | 7 | HG00642.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-1379_1099-137 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730434 | ||||||
chr12:64730512
|
G | A | 7 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0029others(4): Show | 7 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099-1455C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730512 | ||||||
chr12:64730544
|
A | T | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1099-1487T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730544 | ||||||
chr12:64730577
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(250): Show | 269 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1099-1520A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730577 | ||||||
chr12:64730918
|
A | T | 1 | a0001c0002t0002g0043 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1099-1861T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730918 | ||||||
chr12:64730922
|
C | T | 10 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(7): Show | 11 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1099-1865G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730922 | ||||||
chr12:64731319
|
C | T | 2 | a0001c0001t0021g0330a0004c0007t0019g0064 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1099-2262G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731319 | ||||||
chr12:64731413
|
A | T | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1099-2356T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731413 | ||||||
chr12:64731430
|
T | C | 1 | a0004c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1099-2373A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731430 | ||||||
chr12:64731910
|
T | C | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1099-2853A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731910 | ||||||
chr12:64731954
|
G | A | 3 | a0001c0001t0008g0129a0001c0001t0008g0130a0001c0001t0008g0131 | 3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1099-2897C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731954 | ||||||
chr12:64732065
|
C | A | 1 | a0001c0001t0003g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1099-3008G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732065 | ||||||
chr12:64732153
|
A | ATTT | 6 | a0001c0001t0001g0248a0001c0001t0001g0275a0001c0001t0001g0282others(3): Show | 6 | HG00280.hp2 HG02004.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-3099_1099-309 others(7): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTT | 30 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 36 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1099-3100_1099-309 others(8): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTT | 59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0015others(56): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1099-3101_1099-309 others(9): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTT | 52 | a0001c0001t0001g0013a0001c0001t0001g0155a0001c0001t0001g0159others(49): Show | 55 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1099-3102_1099-309 others(10): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTTT | 35 | a0001c0001t0001g0014a0001c0001t0001g0165a0001c0001t0001g0183others(32): Show | 37 | HG00408.hp1 HG00408.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1099-3103_1099-309 others(11): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTTT others(1): Show |
12 | a0001c0001t0001g0158a0001c0001t0001g0166a0001c0001t0001g0218others(9): Show | 12 | HG01109.hp1 HG02523.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099-3104_1099-309 others(12): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0156a0001c0001t0001g0170a0001c0001t0001g0207others(5): Show | 8 | HG00544.hp1 HG01109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-3105_1099-309 others(13): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTTT others(3): Show |
5 | a0001c0001t0001g0182a0001c0001t0001g0327a0001c0001t0003g0210others(2): Show | 5 | HG00741.hp2 HG02738.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-3106_1099-309 others(14): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTTT others(4): Show |
5 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0003g0303others(2): Show | 5 | HG03195.hp1 HG03491.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-3107_1099-309 others(15): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0003g0295a0001c0001t0003g0301 | 2 | HG03492.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1099-3108_1099-309 others(16): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732153
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0003g0195 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1099-3097_1099-309 others(20): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | ||||||
chr12:64732154
|
TTTTTTTT others(8): Show |
T | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1099-3112_1099-309 others(19): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732154 | ||||||
chr12:64732163
|
T | G | 6 | a0001c0001t0006g0118a0001c0001t0015g0018a0001c0002t0002g0035others(3): Show | 7 | HG01175.hp2 HG01257.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-3106A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732163 | ||||||
chr12:64732166
|
G | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(222): Show | 241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1099-3109C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732166 | ||||||
chr12:64732169
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(220): Show | 238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1099-3112C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732169 | ||||||
chr12:64732169
|
GT | G | 25 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(22): Show | 26 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099-3113delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732169 | ||||||
chr12:64732170
|
T | G | 4 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145others(1): Show | 4 | HG01361.hp1 HG01884.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-3113A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732170 | ||||||
chr12:64732175
|
T | G | 7 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(4): Show | 8 | HG01361.hp1 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-3118A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732175 | ||||||
chr12:64732191
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1099-3134C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732191 | ||||||
chr12:64732216
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1099-3159C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732216 | ||||||
chr12:64732255
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0150others(28): Show | 34 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1099-3198G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732255 | ||||||
chr12:64732260
|
C | T | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1099-3203G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732260 | ||||||
chr12:64732308
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(201): Show | 218 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1099-3251G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732308 | ||||||
chr12:64732359
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1099-3302C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732359 | ||||||
chr12:64732404
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1099-3347C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732404 | ||||||
chr12:64732437
|
G | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1099-3380C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732437 | ||||||
chr12:64732460
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0011g0106a0001c0006t0011g0332others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-3403C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732460 | ||||||
chr12:64732907
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(228): Show | 247 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1099-3850T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732907 | ||||||
chr12:64733044
|
G | C | 1 | a0001c0001t0003g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1098+3960C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733044 | ||||||
chr12:64733104
|
G | A | 4 | a0001c0001t0008g0128a0001c0001t0008g0129a0001c0001t0008g0130others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+3900C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733104 | ||||||
chr12:64733144
|
A | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1098+3860T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733144 | ||||||
chr12:64733297
|
C | CA | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(89): Show | 96 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1098+3706dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | ||||||
chr12:64733297
|
C | CAA | 20 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0185others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1098+3705_1098+370 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | ||||||
chr12:64733297
|
CA | C | 25 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0186others(22): Show | 25 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+3706delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | ||||||
chr12:64733297
|
CAA | C | 10 | a0001c0001t0004g0104a0001c0001t0004g0108a0001c0001t0007g0008others(7): Show | 11 | HG00733.hp1 HG01081.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+3705_1098+370 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | ||||||
chr12:64733297
|
CAAA | C | 10 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(7): Show | 11 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+3704_1098+370 others(7): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | ||||||
chr12:64733297
|
CAAAA | C | 6 | a0001c0002t0004g0051a0002c0005t0004g0063a0002c0005t0004g0100others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+3703_1098+370 others(8): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | ||||||
chr12:64733329
|
T | A | 1 | a0001c0001t0001g0257 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1098+3675A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733329 | ||||||
chr12:64733589
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1098+3415C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733589 | ||||||
chr12:64733745
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1098+3259C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733745 | ||||||
chr12:64733894
|
T | C | 1 | a0001c0002t0012g0085 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1098+3110A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733894 | ||||||
chr12:64734066
|
C | T | 9 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1098+2938G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734066 | ||||||
chr12:64734072
|
T | C | 13 | a0001c0001t0011g0106a0001c0004t0005g0119a0001c0004t0005g0120others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+2932A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734072 | ||||||
chr12:64734275
|
A | T | 1 | a0001c0001t0003g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1098+2729T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734275 | ||||||
chr12:64734400
|
G | A | 5 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+2604C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734400 | ||||||
chr12:64734452
|
C | T | 1 | a0001c0002t0002g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1098+2552G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734452 | ||||||
chr12:64734570
|
C | T | 1 | a0001c0003t0002g0006 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1098+2434G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734570 | ||||||
chr12:64734839
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1098+2165C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734839 | ||||||
chr12:64734929
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1098+2075G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734929 | ||||||
chr12:64735188
|
G | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1098+1816C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64735188 | ||||||
chr12:64735640
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1098+1364G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64735640 | ||||||
chr12:64736062
|
T | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1098+942A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736062 | ||||||
chr12:64736110
|
T | C | 1 | a0001c0001t0003g0192 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1098+894A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736110 | ||||||
chr12:64736115
|
A | T | 2 | a0001c0001t0021g0330a0004c0007t0019g0064 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1098+889T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736115 | ||||||
chr12:64736122
|
G | T | 2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1098+882C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736122 | ||||||
chr12:64736159
|
C | A | 1 | a0001c0003t0002g0054 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1098+845G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736159 | ||||||
chr12:64736202
|
C | T | 5 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+802G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736202 | ||||||
chr12:64736469
|
G | C | 3 | a0001c0001t0008g0129a0001c0001t0008g0130a0001c0001t0008g0131 | 3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1098+535C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736469 | ||||||
chr12:64736643
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(250): Show | 269 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1098+361A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736643 | ||||||
chr12:64736940
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1098+64C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736940 | ||||||
chr12:64737930
|
C | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.995-823G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64737930 | ||||||
chr12:64738036
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.995-929C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738036 | ||||||
chr12:64738135
|
G | A | 3 | a0001c0001t0011g0106a0001c0006t0011g0332a0001c0006t0011g0333 | 3 | HG02559.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.995-1028C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738135 | ||||||
chr12:64738156
|
T | A | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.995-1049A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738156 | ||||||
chr12:64738353
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1028G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738353 | ||||||
chr12:64738359
|
T | C | 1 | a0001c0001t0003g0317 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.994+1022A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738359 | ||||||
chr12:64738539
|
C | T | 14 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.994+842G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738539 | ||||||
chr12:64738674
|
G | A | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994+707C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738674 | ||||||
chr12:64738761
|
C | T | 2 | a0001c0001t0021g0330a0004c0007t0019g0064 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.994+620G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738761 | ||||||
chr12:64738815
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02027.hp2 NA18747.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+566G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738815 | ||||||
chr12:64738825
|
C | CA | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(206): Show | 224 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.994+555_994+556ins others(1): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738825 | ||||||
chr12:64738826
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(207): Show | 225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.994+555G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738826 | ||||||
chr12:64738826
|
C | CA | 26 | a0001c0001t0001g0165a0001c0001t0001g0234a0001c0001t0001g0327others(23): Show | 26 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.994+554dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738826 | ||||||
chr12:64738827
|
A | C | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.994+554T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738827 | ||||||
chr12:64738847
|
T | C | 3 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145 | 3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.994+534A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738847 | ||||||
chr12:64738946
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.994+435T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738946 | ||||||
chr12:64739181
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0274 | 2 | NA18960.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.994+200C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739181 | ||||||
chr12:64739197
|
T | A | 1 | a0001c0001t0003g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.994+184A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739197 | ||||||
chr12:64739202
|
C | T | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.994+179G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739202 | ||||||
chr12:64739228
|
T | C | 2 | a0001c0001t0021g0330a0004c0007t0019g0064 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.994+153A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739228 | ||||||
chr12:64739502
|
G | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.876-3C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739502 | ||||||
chr12:64739564
|
C | CA | 18 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0172others(15): Show | 18 | HG00639.hp1 HG01106.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-66dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739564 | ||||||
chr12:64739585
|
A | C | 3 | a0001c0002t0002g0022a0001c0002t0002g0026a0001c0002t0002g0071 | 3 | NA18943.hp1 NA18953.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.876-86T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739585 | ||||||
chr12:64739681
|
C | T | 13 | a0001c0001t0011g0106a0001c0004t0005g0119a0001c0004t0005g0120others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.876-182G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739681 | ||||||
chr12:64739849
|
G | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0322 | 3 | HG02280.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.876-350C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739849 | ||||||
chr12:64739864
|
C | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(120): Show | 131 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.876-365G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739864 | ||||||
chr12:64740089
|
G | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.875+517C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64740089 | ||||||
chr12:64740485
|
C | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.875+121G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64740485 | ||||||
chr12:64740756
|
C | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(245): Show | 263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.793-68G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64740756 | ||||||
chr12:64741047
|
TAGAAAAT others(169): Show |
T | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(250): Show | 269 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.793-535_793-360del | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741047 | ||||||
chr12:64741268
|
T | C | 3 | a0001c0001t0003g0301a0001c0001t0003g0302a0001c0001t0003g0303 | 3 | HG03491.hp1 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.793-580A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741268 | ||||||
chr12:64741320
|
C | T | 1 | a0001c0001t0004g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.793-632G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741320 | ||||||
chr12:64741354
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.793-666G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741354 | ||||||
chr12:64741407
|
A | G | 2 | a0001c0001t0021g0330a0004c0007t0019g0064 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.793-719T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741407 | ||||||
chr12:64741491
|
C | T | 1 | a0001c0001t0003g0305 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.793-803G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741491 | ||||||
chr12:64741590
|
T | C | 1 | a0001c0002t0018g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.793-902A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741590 | ||||||
chr12:64741742
|
C | T | 1 | a0004c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.793-1054G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741742 | ||||||
chr12:64742057
|
G | A | 1 | a0001c0002t0002g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.792+1084C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742057 | ||||||
chr12:64742114
|
G | A | 2 | a0001c0001t0014g0065a0001c0001t0014g0066 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792+1027C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742114 | ||||||
chr12:64742158
|
G | C | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.792+983C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742158 | ||||||
chr12:64742210
|
T | C | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.792+931A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742210 | ||||||
chr12:64742216
|
T | G | 3 | a0001c0001t0008g0129a0001c0001t0008g0130a0001c0001t0008g0131 | 3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.792+925A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742216 | ||||||
chr12:64742221
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0304 | 2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.792+920A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742221 | ||||||
chr12:64742239
|
C | T | 1 | a0001c0001t0001g0258 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.792+902G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742239 | ||||||
chr12:64742242
|
A | G | 4 | a0001c0001t0001g0257a0001c0001t0004g0144a0001c0001t0004g0145others(1): Show | 4 | HG01256.hp2 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+899T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742242 | ||||||
chr12:64742255
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.792+886G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742255 | ||||||
chr12:64742261
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.792+880A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742261 | ||||||
chr12:64742266
|
C | G | 5 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0004t0005g0120others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+875G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742266 | ||||||
chr12:64742271
|
T | C | 1 | a0004c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.792+870A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742271 | ||||||
chr12:64742299
|
C | T | 2 | a0001c0003t0002g0067a0001c0003t0002g0090 | 2 | HG01123.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.792+842G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742299 | ||||||
chr12:64742300
|
A | G | 5 | a0001c0001t0008g0129a0001c0001t0008g0130a0001c0001t0008g0131others(2): Show | 5 | HG00733.hp1 HG01081.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+841T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742300 | ||||||
chr12:64742312
|
G | A | 1 | a0001c0002t0020g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.792+829C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742312 | ||||||
chr12:64742413
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(132): Show | 144 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.792+728A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742413 | ||||||
chr12:64742415
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.792+726A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742415 | ||||||
chr12:64742743
|
C | G | 1 | a0001c0001t0003g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.792+398G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742743 | ||||||
chr12:64742774
|
C | T | 2 | a0001c0001t0014g0065a0001c0001t0014g0066 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792+367G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742774 | ||||||
chr12:64742847
|
G | A | 2 | a0001c0001t0014g0065a0001c0001t0014g0066 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792+294C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742847 | ||||||
chr12:64743062
|
G | A | 1 | a0001c0003t0002g0054 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.792+79C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743062 | ||||||
chr12:64743087
|
C | G | 2 | a0001c0003t0002g0077a0001c0003t0002g0089 | 2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.792+54G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743087 | ||||||
chr12:64743116
|
G | C | 3 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145 | 3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.792+25C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743116 | ||||||
chr12:64743125
|
T | C | 2 | a0001c0001t0021g0330a0004c0007t0019g0064 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.792+16A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743125 | ||||||
chr12:64743356
|
G | A | 10 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(7): Show | 11 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-48C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743356 | ||||||
chr12:64743385
|
G | T | 8 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-77C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743385 | ||||||
chr12:64743626
|
A | T | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.625-318T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743626 | ||||||
chr12:64743631
|
G | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.625-323C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743631 | ||||||
chr12:64743673
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.625-365T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743673 | ||||||
chr12:64743731
|
T | C | 2 | a0001c0001t0014g0065a0001c0001t0014g0066 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.625-423A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743731 | ||||||
chr12:64743921
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0243 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.625-613G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743921 | ||||||
chr12:64744201
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(243): Show | 262 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.624+608C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744201 | ||||||
chr12:64744352
|
A | G | 1 | a0001c0002t0003g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.624+457T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744352 | ||||||
chr12:64744474
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.624+335A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744474 | ||||||
chr12:64744501
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.624+308T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744501 | ||||||
chr12:64744542
|
TC | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.624+266delG | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744542 | ||||||
chr12:64744555
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.624+254T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744555 | ||||||
chr12:64745032
|
A | G | 1 | a0001c0002t0002g0020 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.526-125T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745032 | ||||||
chr12:64745136
|
C | G | 2 | a0001c0002t0002g0048a0001c0002t0002g0049 | 2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.526-229G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745136 | ||||||
chr12:64745164
|
G | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.526-257C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745164 | ||||||
chr12:64745204
|
CT | C | 65 | a0001c0001t0001g0154a0001c0001t0001g0163a0001c0001t0001g0215others(62): Show | 67 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.526-298delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | ||||||
chr12:64745204
|
CTT | C | 62 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0170others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.526-299_526-298del others(2): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | ||||||
chr12:64745204
|
CTTT | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(163): Show | 182 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.526-300_526-298del others(3): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | ||||||
chr12:64745204
|
CTTTT | C | 9 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(6): Show | 9 | HG00280.hp2 HG00544.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-301_526-298del others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | ||||||
chr12:64745204
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0008g0129a0001c0001t0008g0130a0001c0001t0008g0131 | 3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.526-307_526-298del others(10): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | ||||||
chr12:64745204
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.526-312_526-298del others(15): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | ||||||
chr12:64745218
|
T | G | 3 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145 | 3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.526-311A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745218 | ||||||
chr12:64745314
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.525+345C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745314 | ||||||
chr12:64745484
|
T | C | 1 | a0001c0001t0011g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.525+175A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745484 | ||||||
chr12:64745625
|
C | T | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.525+34G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745625 | ||||||
chr12:64746004
|
A | G | 2 | a0001c0006t0011g0332a0001c0006t0011g0333 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.460-280T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64746004 | ||||||
chr12:64746212
|
TCCACACA others(7): Show |
T | 23 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.460-502_460-489del others(14): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64746212 | ||||||
chr12:64746340
|
G | A | 2 | a0001c0006t0011g0332a0001c0006t0011g0333 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.460-616C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64746340 | ||||||
chr12:64747021
|
G | C | 23 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.459+691C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747021 | ||||||
chr12:64747076
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.459+636C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747076 | ||||||
chr12:64747186
|
C | T | 10 | a0001c0004t0005g0119a0001c0004t0005g0120a0001c0004t0005g0121others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.459+526G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747186 | ||||||
chr12:64747340
|
T | C | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.459+372A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747340 | ||||||
chr12:64747531
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.459+181A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747531 | ||||||
chr12:64747571
|
G | A | 3 | a0001c0001t0003g0198a0001c0001t0003g0285a0001c0001t0003g0296 | 3 | HG00408.hp2 HG01978.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.459+141C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747571 | ||||||
chr12:64747698
|
A | G | 8 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+14T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747698 | ||||||
chr12:64747942
|
C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.253-24G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64747942 | ||||||
chr12:64747989
|
A | G | 4 | a0001c0001t0008g0128a0001c0001t0008g0129a0001c0001t0008g0130others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-71T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64747989 | ||||||
chr12:64748034
|
C | T | 23 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.253-116G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748034 | ||||||
chr12:64748191
|
G | A | 35 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(32): Show | 36 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.253-273C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748191 | ||||||
chr12:64748199
|
AGTT | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.253-284_253-282del others(3): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748199 | ||||||
chr12:64748417
|
C | T | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253-499G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748417 | ||||||
chr12:64748634
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.253-716T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748634 | ||||||
chr12:64748700
|
T | C | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253-782A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748700 | ||||||
chr12:64748771
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.253-853T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748771 | ||||||
chr12:64748844
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0154a0001c0001t0001g0185 | 4 | HG02257.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-926C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748844 | ||||||
chr12:64748960
|
G | A | 4 | a0001c0001t0008g0128a0001c0001t0008g0129a0001c0001t0008g0130others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-1042C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748960 | ||||||
chr12:64748962
|
T | G | 35 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(32): Show | 36 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.253-1044A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748962 | ||||||
chr12:64748964
|
G | A | 4 | a0001c0001t0008g0128a0001c0001t0008g0129a0001c0001t0008g0130others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-1046C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748964 | ||||||
chr12:64748970
|
C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.253-1052G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748970 | ||||||
chr12:64748980
|
C | T | 2 | a0001c0002t0002g0068a0001c0002t0002g0096 | 2 | HG00140.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.253-1062G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748980 | ||||||
chr12:64749001
|
G | A | 1 | a0001c0002t0001g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.253-1083C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749001 | ||||||
chr12:64749033
|
G | A | 3 | a0001c0001t0006g0132a0001c0001t0006g0136a0001c0001t0006g0140 | 3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.253-1115C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749033 | ||||||
chr12:64749089
|
G | A | 1 | a0001c0002t0002g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.253-1171C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749089 | ||||||
chr12:64749182
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(262): Show | 281 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.253-1264T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749182 | ||||||
chr12:64749248
|
C | CT | 16 | a0001c0001t0001g0154a0001c0001t0001g0165a0001c0001t0001g0166others(13): Show | 16 | HG00423.hp1 HG01255.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-1331dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749248 | ||||||
chr12:64749248
|
CT | C | 76 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0004g0007others(73): Show | 79 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.253-1331delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749248 | ||||||
chr12:64749248
|
CTT | C | 56 | a0001c0002t0001g0028a0001c0002t0001g0041a0001c0002t0001g0042others(53): Show | 58 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.253-1332_253-1331d others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749248 | ||||||
chr12:64749336
|
T | C | 2 | a0001c0006t0011g0332a0001c0006t0011g0333 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.253-1418A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749336 | ||||||
chr12:64749363
|
C | T | 5 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-1445G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749363 | ||||||
chr12:64749366
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.253-1448G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749366 | ||||||
chr12:64749409
|
C | T | 9 | a0001c0001t0001g0222a0001c0001t0004g0007a0001c0001t0004g0099others(6): Show | 10 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-1491G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749409 | ||||||
chr12:64749410
|
G | A | 5 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-1492C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749410 | ||||||
chr12:64749551
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.253-1633G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749551 | ||||||
chr12:64749602
|
A | G | 143 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(140): Show | 148 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.253-1684T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749602 | ||||||
chr12:64749623
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG00423.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.253-1705G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749623 | ||||||
chr12:64749668
|
G | A | 1 | a0001c0004t0005g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.253-1750C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749668 | ||||||
chr12:64749729
|
A | G | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-1811T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749729 | ||||||
chr12:64749776
|
T | C | 2 | a0001c0006t0011g0332a0001c0006t0011g0333 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.253-1858A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749776 | ||||||
chr12:64749873
|
A | AT | 125 | a0001c0001t0001g0162a0001c0001t0001g0327a0001c0001t0004g0143others(122): Show | 129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.253-1956dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749873 | ||||||
chr12:64749921
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.253-2003C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749921 | ||||||
chr12:64750028
|
C | A | 1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.253-2110G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750028 | ||||||
chr12:64750187
|
T | C | 6 | a0001c0001t0001g0186a0001c0001t0007g0008a0001c0001t0007g0114others(3): Show | 7 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-2269A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750187 | ||||||
chr12:64750196
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.253-2278C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750196 | ||||||
chr12:64750255
|
G | C | 1 | a0001c0001t0001g0288 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.253-2337C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750255 | ||||||
chr12:64750384
|
T | C | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252+2314A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750384 | ||||||
chr12:64750495
|
A | T | 142 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(139): Show | 147 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.252+2203T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750495 | ||||||
chr12:64750631
|
C | T | 4 | a0001c0001t0008g0128a0001c0001t0008g0129a0001c0001t0008g0130others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+2067G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750631 | ||||||
chr12:64750658
|
A | G | 1 | a0004c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.252+2040T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750658 | ||||||
chr12:64750679
|
G | A | 35 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(32): Show | 36 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.252+2019C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750679 | ||||||
chr12:64750704
|
A | G | 23 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.252+1994T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750704 | ||||||
chr12:64750811
|
C | T | 4 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145others(1): Show | 4 | HG01884.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1887G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750811 | ||||||
chr12:64750812
|
G | A | 23 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.252+1886C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750812 | ||||||
chr12:64750855
|
T | C | 1 | a0001c0002t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.252+1843A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750855 | ||||||
chr12:64750955
|
C | T | 2 | a0001c0001t0014g0065a0001c0001t0014g0066 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.252+1743G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750955 | ||||||
chr12:64750984
|
G | T | 1 | a0001c0001t0001g0010 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.252+1714C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750984 | ||||||
chr12:64751132
|
G | A | 5 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+1566C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751132 | ||||||
chr12:64751343
|
C | A | 10 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(7): Show | 11 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.252+1355G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751343 | ||||||
chr12:64751375
|
A | G | 1 | a0001c0002t0003g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.252+1323T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751375 | ||||||
chr12:64751444
|
G | A | 4 | a0001c0001t0008g0128a0001c0001t0008g0129a0001c0001t0008g0130others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1254C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751444 | ||||||
chr12:64751599
|
C | T | 33 | a0001c0002t0001g0028a0001c0002t0001g0041a0001c0002t0001g0042others(30): Show | 34 | HG01175.hp2 HG01361.hp2 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.252+1099G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751599 | ||||||
chr12:64751637
|
C | T | 1 | a0004c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.252+1061G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751637 | ||||||
chr12:64751660
|
T | C | 3 | a0001c0002t0002g0005a0001c0002t0002g0057a0001c0002t0002g0091 | 4 | HG02155.hp1 NA18966.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1038A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751660 | ||||||
chr12:64751787
|
G | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.252+911C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751787 | ||||||
chr12:64751951
|
C | CA | 27 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0325others(24): Show | 30 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.252+746dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751951 | ||||||
chr12:64751951
|
CA | C | 10 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0003g0294others(7): Show | 10 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.252+746delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751951 | ||||||
chr12:64752102
|
TTAAA | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.252+592_252+595del others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752102 | ||||||
chr12:64752324
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.252+374T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752324 | ||||||
chr12:64752507
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.252+191A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752507 | ||||||
chr12:64752511
|
C | T | 2 | a0001c0006t0011g0332a0001c0006t0011g0333 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.252+187G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752511 | ||||||
chr12:64752896
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.193-139A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64752896 | ||||||
chr12:64753009
|
G | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | NA18747.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.193-252C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753009 | ||||||
chr12:64753079
|
G | A | 4 | a0001c0002t0002g0038a0001c0002t0002g0058a0001c0002t0002g0092others(1): Show | 4 | HG00735.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-322C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753079 | ||||||
chr12:64753591
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(208): Show | 226 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.193-834A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753591 | ||||||
chr12:64753600
|
G | T | 1 | a0001c0004t0005g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193-843C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753600 | ||||||
chr12:64753633
|
T | C | 2 | a0001c0001t0006g0118a0001c0001t0006g0142 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-876A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753633 | ||||||
chr12:64753778
|
A | T | 1 | a0001c0001t0009g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-1021T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753778 | ||||||
chr12:64753902
|
T | C | 1 | a0001c0001t0003g0319 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.193-1145A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753902 | ||||||
chr12:64753921
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.193-1164T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753921 | ||||||
chr12:64753976
|
G | A | 4 | a0001c0001t0008g0128a0001c0001t0008g0129a0001c0001t0008g0130others(1): Show | 4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1219C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753976 | ||||||
chr12:64754209
|
T | C | 10 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0136others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-1452A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754209 | ||||||
chr12:64754333
|
T | C | 5 | a0001c0002t0002g0039a0001c0002t0002g0059a0001c0002t0002g0094others(2): Show | 5 | HG01361.hp2 HG01975.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-1576A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754333 | ||||||
chr12:64754691
|
C | T | 2 | a0001c0006t0011g0332a0001c0006t0011g0333 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.193-1934G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754691 | ||||||
chr12:64754734
|
T | C | 1 | a0001c0002t0002g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.193-1977A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754734 | ||||||
chr12:64754805
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(245): Show | 264 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.193-2048A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754805 | ||||||
chr12:64754813
|
C | G | 1 | a0001c0001t0001g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.193-2056G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754813 | ||||||
chr12:64754890
|
C | CA | 53 | a0001c0001t0001g0293a0001c0001t0001g0304a0001c0001t0001g0311others(50): Show | 56 | HG00140.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.193-2134dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754890 | ||||||
chr12:64754902
|
AAAG | A | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.193-2148_193-2146d others(5): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754902 | ||||||
chr12:64755077
|
T | C | 1 | a0001c0002t0002g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.193-2320A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755077 | ||||||
chr12:64755317
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.193-2560G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755317 | ||||||
chr12:64755331
|
C | A | 33 | a0001c0001t0006g0118a0001c0001t0006g0134a0001c0001t0006g0136others(30): Show | 34 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.193-2574G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755331 | ||||||
chr12:64755439
|
G | A | 1 | a0004c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.193-2682C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755439 | ||||||
chr12:64755532
|
C | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.193-2775G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755532 | ||||||
chr12:64755577
|
C | CA | 7 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0001t0004g0144others(4): Show | 7 | HG00558.hp2 HG01175.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2821dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755577 | ||||||
chr12:64755577
|
CA | C | 11 | a0001c0001t0006g0118a0001c0001t0006g0134a0001c0001t0006g0136others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-2821delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755577 | ||||||
chr12:64755678
|
A | AT | 39 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0155others(36): Show | 41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.193-2922dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755678 | ||||||
chr12:64755752
|
C | T | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-2995G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755752 | ||||||
chr12:64755755
|
T | C | 1 | a0001c0002t0002g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.193-2998A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755755 | ||||||
chr12:64755845
|
A | AT | 9 | a0001c0004t0005g0119a0001c0004t0005g0120a0001c0004t0005g0121others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-3089dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755845 | ||||||
chr12:64755866
|
G | A | 3 | a0001c0001t0003g0199a0001c0001t0003g0320a0001c0001t0003g0321 | 3 | HG00642.hp1 HG01433.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.193-3109C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755866 | ||||||
chr12:64755997
|
T | C | 17 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(14): Show | 18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+3088A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755997 | ||||||
chr12:64756064
|
A | T | 1 | a0001c0001t0006g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192+3021T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756064 | ||||||
chr12:64756232
|
A | T | 1 | a0001c0001t0006g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192+2853T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756232 | ||||||
chr12:64756393
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.192+2692C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756393 | ||||||
chr12:64756458
|
T | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(9): Show | 13 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+2627A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756458 | ||||||
chr12:64756562
|
G | A | 2 | a0001c0001t0003g0323a0001c0001t0003g0324 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.192+2523C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756562 | ||||||
chr12:64756705
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(245): Show | 264 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.192+2380G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756705 | ||||||
chr12:64756746
|
G | A | 22 | a0001c0001t0006g0118a0001c0001t0006g0132a0001c0001t0006g0134others(19): Show | 22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.192+2339C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756746 | ||||||
chr12:64756898
|
T | C | 1 | a0001c0002t0002g0098 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.192+2187A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756898 | ||||||
chr12:64756982
|
C | T | 2 | a0001c0001t0014g0065a0001c0001t0014g0066 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.192+2103G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756982 | ||||||
chr12:64757082
|
G | C | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+2003C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757082 | ||||||
chr12:64757146
|
T | C | 1 | a0001c0001t0003g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.192+1939A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757146 | ||||||
chr12:64757194
|
G | C | 10 | a0001c0001t0004g0007a0001c0001t0004g0099a0001c0001t0004g0103others(7): Show | 11 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+1891C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757194 | ||||||
chr12:64757222
|
A | T | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+1863T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757222 | ||||||
chr12:64757293
|
C | T | 1 | a0004c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.192+1792G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757293 | ||||||
chr12:64757785
|
C | T | 2 | a0001c0003t0002g0033a0001c0003t0002g0034 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.192+1300G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757785 | ||||||
chr12:64757847
|
C | A | 9 | a0001c0004t0005g0119a0001c0004t0005g0120a0001c0004t0005g0121others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+1238G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757847 | ||||||
chr12:64757911
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.192+1174G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757911 | ||||||
chr12:64758073
|
G | A | 1 | a0001c0002t0002g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.192+1012C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758073 | ||||||
chr12:64758162
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG00323.hp2 HG01346.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+923G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758162 | ||||||
chr12:64758204
|
C | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(206): Show | 224 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.192+881G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758204 | ||||||
chr12:64758230
|
G | A | 1 | a0001c0001t0004g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.192+855C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758230 | ||||||
chr12:64758309
|
C | CT | 32 | a0001c0002t0001g0036a0001c0002t0001g0041a0001c0002t0001g0042others(29): Show | 34 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.192+775dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
C | CTT | 14 | a0001c0002t0001g0028a0001c0002t0002g0019a0001c0002t0002g0020others(11): Show | 14 | HG00621.hp2 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+774_192+775dup others(2): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTT | C | 50 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0155others(47): Show | 50 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+772_192+775del others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTT | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(142): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.192+771_192+775del others(5): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTT | C | 8 | a0001c0001t0001g0325a0001c0001t0003g0326a0001c0001t0004g0007others(5): Show | 9 | HG01243.hp1 HG02080.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+770_192+775del others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0007g0008a0001c0001t0007g0114a0001c0001t0007g0115others(2): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+765_192+775del others(11): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTTT others(5): Show |
C | 11 | a0001c0001t0001g0327a0001c0001t0006g0118a0001c0004t0005g0119others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+764_192+775del others(12): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTTT others(6): Show |
C | 15 | a0001c0001t0006g0132a0001c0001t0006g0134a0001c0001t0006g0136others(12): Show | 15 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+763_192+775del others(13): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+762_192+775del others(14): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0004g0143a0001c0001t0004g0144 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.192+761_192+775del others(15): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0004g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+760_192+775del others(16): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758309
|
CTTTTTTT others(10): Show |
C | 5 | a0001c0002t0002g0146a0001c0002t0002g0147a0001c0002t0002g0148others(2): Show | 5 | HG01255.hp1 HG01515.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+759_192+775del others(17): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | ||||||
chr12:64758386
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(187): Show | 204 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.192+699C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758386 | ||||||
chr12:64758716
|
C | G | 1 | a0001c0002t0002g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+369G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758716 | ||||||
chr12:64758717
|
T | G | 1 | a0001c0002t0002g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+368A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758717 | ||||||
chr12:64758734
|
A | G | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+351T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758734 | ||||||
chr12:64758776
|
G | C | 1 | a0001c0002t0002g0329 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.192+309C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758776 | ||||||
chr12:64758918
|
T | C | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.192+167A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758918 | ||||||
chr12:64758972
|
C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+113G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758972 | ||||||
chr12:64759005
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.192+80C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64759005 |