geneid | 25926 |
---|---|
ensemblid | ENSG00000130935.10 |
hgncid | 24557 |
symbol | NOL11 |
name | nucleolar protein 11 |
refseq_nuc | NM_015462.5 |
refseq_prot | NP_056277.2 |
ensembl_nuc | ENST00000253247.9 |
ensembl_prot | ENSP00000253247.4 |
mane_status | MANE Select |
chr | chr17 |
start | 67717936 |
end | 67744531 |
strand | + |
ver | v1.2 |
region | chr17:67717936-67744531 |
region5000 | chr17:67712936-67749531 |
regionname0 | NOL11_chr17_67717936_67744531 |
regionname5000 | NOL11_chr17_67712936_67749531 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 719 | 317 | 79 | 64 | 125 | 10 | 37 | 96 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0002 | 0/0 | 719 | 55 | 0 | 2 | 52 | 0 | 1 | 42 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0003 | 0/0 | 719 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0004 | 0/0 | 719 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0005 | 0/0 | 719 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0006 | 0/0 | 719 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0007 | 0/0 | 719 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0008 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0009 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0010 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0011 | 0/0 | 719 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2160 | 156 | 28 | 34 | 76 | 4 | 14 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0002 | 1/0 | 2160 | 115 | 45 | 22 | 21 | 4 | 22 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0003 | 0/0 | 2160 | 55 | 0 | 2 | 52 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0004 | 0/1 | 2160 | 40 | 5 | 6 | 26 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0005 | 0/0 | 2160 | 10 | 9 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0006 | 0/0 | 2160 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0007 | 0/0 | 2160 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0008 | 0/0 | 2160 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0009 | 0/0 | 2160 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0010 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0011 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0012 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0013 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0014 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0015 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0016 | 0/0 | 2160 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0017 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0018 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
c0019 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 685 | 314 | 50 | 53 | 168 | 10 | 32 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0002 | 1/0 | 685 | 49 | 25 | 14 | 3 | 0 | 6 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0003 | 0/0 | 685 | 15 | 14 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0004 | 0/0 | 685 | 6 | 0 | 0 | 6 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0005 | 0/0 | 685 | 3 | 3 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0006 | 0/0 | 685 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0007 | 0/0 | 685 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0008 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0009 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
t0010 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 1 | 4 | 16 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0002 | 0/0 | 18 | 0 | 2 | 16 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0003 | 0/0 | 17 | 1 | 2 | 14 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0004 | 0/0 | 10 | 3 | 3 | 2 | 1 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0005 | 0/0 | 10 | 1 | 2 | 1 | 2 | 4 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0006 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0007 | 0/0 | 6 | 2 | 0 | 3 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0008 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0026 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0027 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0052 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2160 | 156 | 28 | 34 | 76 | 4 | 14 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0002 | 1/0 | 2160 | 115 | 45 | 22 | 21 | 4 | 22 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0004 | 0/1 | 2160 | 40 | 5 | 6 | 26 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0009 | 0/0 | 2160 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0013 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0014 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0016 | 0/0 | 2160 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0018 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0002c0003 | 0/0 | 2160 | 55 | 0 | 2 | 52 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0003c0005 | 0/0 | 2160 | 10 | 9 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0004c0006 | 0/0 | 2160 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0004c0012 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0005c0007 | 0/0 | 2160 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0006c0008 | 0/0 | 2160 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0007c0019 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0008c0010 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0009c0015 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0010c0017 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0011c0011 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2844 | 152 | 28 | 34 | 72 | 4 | 14 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0001t0006 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0001t0007 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0002t0001 | 0/0 | 2844 | 60 | 14 | 8 | 18 | 4 | 16 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0002t0002 | 1/0 | 2844 | 48 | 24 | 14 | 3 | 0 | 6 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0002t0003 | 0/0 | 2844 | 5 | 5 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0002t0008 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0002t0010 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0004t0001 | 0/1 | 2844 | 34 | 5 | 6 | 20 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0004t0004 | 0/0 | 2844 | 6 | 0 | 0 | 6 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0009t0001 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0013t0002 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0014t0001 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0016t0001 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0001c0018t0001 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0002c0003t0001 | 0/0 | 2844 | 54 | 0 | 2 | 51 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0002c0003t0009 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0003c0005t0003 | 0/0 | 2844 | 10 | 9 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0004c0006t0005 | 0/0 | 2844 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0004c0012t0005 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0005c0007t0001 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0006c0008t0001 | 0/0 | 2844 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0007c0019t0001 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0008c0010t0001 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0009c0015t0001 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0010c0017t0001 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
a0011c0011t0001 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | copy fasta | chr17 | 67712936 | 67749531 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 1 | 4 | 14 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0003 | 0/0 | 14 | 1 | 2 | 11 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0004 | 0/0 | 9 | 3 | 3 | 2 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0005 | 0/0 | 10 | 1 | 2 | 1 | 2 | 4 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0026 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0002t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0007 | 0/0 | 6 | 2 | 0 | 3 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0027 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0052 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0004t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0009t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0013t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0014t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0016t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0001c0018t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0002 | 0/0 | 18 | 0 | 2 | 16 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0002c0003t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0003c0005t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0003c0005t0003g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0003c0005t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0003c0005t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0003c0005t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0004c0006t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0004c0012t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0005c0007t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0006c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0006c0008t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0007c0019t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0008c0010t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0009c0015t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0010c0017t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
a0011c0011t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0007 | EUR | GBR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0027 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00408 | hp1 | a0001 | c0004 | t0001 | g0224 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00408 | hp2 | a0001 | c0004 | t0001 | g0220 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00438 | hp2 | a0002 | c0003 | t0001 | g0179 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00544 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0172 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00621 | hp2 | a0001 | c0004 | t0001 | g0051 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0229 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01109 | hp1 | a0003 | c0005 | t0003 | g0025 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0051 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01243 | hp2 | a0001 | c0004 | t0001 | g0232 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01255 | hp1 | a0001 | c0004 | t0001 | g0027 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01257 | hp2 | a0001 | c0004 | t0001 | g0213 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01358 | hp1 | a0001 | c0018 | t0001 | g0033 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01496 | hp1 | a0001 | c0014 | t0001 | g0127 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0041 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0041 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01884 | hp2 | a0004 | c0006 | t0005 | g0018 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01934 | hp2 | a0011 | c0011 | t0001 | g0009 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01952 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0171 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02040 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02056 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02071 | hp1 | a0001 | c0004 | t0001 | g0230 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02080 | hp1 | a0001 | c0004 | t0001 | g0052 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02148 | hp2 | a0001 | c0004 | t0001 | g0052 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02165 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02257 | hp2 | a0003 | c0005 | t0003 | g0194 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0063 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0077 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02723 | hp1 | a0001 | c0002 | t0003 | g0049 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02723 | hp2 | a0006 | c0008 | t0001 | g0125 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02886 | hp1 | a0003 | c0005 | t0003 | g0012 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02896 | hp2 | a0001 | c0002 | t0003 | g0216 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02922 | hp1 | a0001 | c0002 | t0003 | g0215 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02922 | hp2 | a0006 | c0008 | t0001 | g0124 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02965 | hp1 | a0004 | c0006 | t0005 | g0018 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02970 | hp2 | a0007 | c0019 | t0001 | g0068 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02976 | hp2 | a0003 | c0005 | t0003 | g0025 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0207 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03098 | hp1 | a0001 | c0013 | t0002 | g0071 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03130 | hp2 | a0004 | c0012 | t0005 | g0018 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0211 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0197 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03209 | hp1 | a0003 | c0005 | t0003 | g0193 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03486 | hp2 | a0001 | c0002 | t0010 | g0050 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03540 | hp2 | a0003 | c0005 | t0003 | g0012 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0209 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0199 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03942 | hp1 | a0001 | c0016 | t0001 | g0004 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0170 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0185 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18522 | hp1 | a0001 | c0002 | t0008 | g0195 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18612 | hp1 | a0010 | c0017 | t0001 | g0106 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0210 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18906 | hp2 | a0003 | c0005 | t0003 | g0012 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18940 | hp1 | a0001 | c0009 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18940 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18941 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18944 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18945 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18946 | hp1 | a0002 | c0003 | t0009 | g0020 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18947 | hp2 | a0001 | c0004 | t0004 | g0238 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18948 | hp1 | a0001 | c0004 | t0001 | g0218 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18950 | hp2 | a0001 | c0004 | t0004 | g0239 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18954 | hp2 | a0009 | c0015 | t0001 | g0085 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18956 | hp2 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18957 | hp2 | a0001 | c0004 | t0004 | g0235 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18959 | hp2 | a0001 | c0004 | t0004 | g0240 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18960 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18962 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18964 | hp1 | a0005 | c0007 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18968 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0180 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0177 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18978 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18979 | hp1 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18981 | hp1 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18981 | hp2 | a0008 | c0010 | t0001 | g0181 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18983 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18985 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18987 | hp2 | a0001 | c0004 | t0001 | g0233 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18989 | hp1 | a0002 | c0003 | t0001 | g0186 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18994 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18997 | hp1 | a0001 | c0004 | t0001 | g0219 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA18999 | hp2 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19001 | hp2 | a0001 | c0004 | t0001 | g0222 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19002 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0176 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19005 | hp2 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19007 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19009 | hp2 | a0001 | c0004 | t0001 | g0141 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19010 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0184 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19012 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19030 | hp2 | a0003 | c0005 | t0003 | g0025 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19043 | hp2 | a0003 | c0005 | t0003 | g0012 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19055 | hp1 | a0002 | c0003 | t0001 | g0173 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19056 | hp1 | a0001 | c0004 | t0001 | g0212 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19057 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19064 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19065 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19070 | hp2 | a0001 | c0004 | t0004 | g0237 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19072 | hp1 | a0002 | c0003 | t0001 | g0175 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19075 | hp2 | a0002 | c0003 | t0001 | g0174 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19077 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19078 | hp2 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19082 | hp2 | a0001 | c0004 | t0001 | g0221 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19084 | hp1 | a0005 | c0007 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19086 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19086 | hp2 | a0001 | c0009 | t0001 | g0017 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19087 | hp1 | a0001 | c0004 | t0004 | g0236 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19087 | hp2 | a0002 | c0003 | t0001 | g0178 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19088 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19089 | hp1 | a0002 | c0003 | t0001 | g0187 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0027 | AFR | ASW | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | GIH | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02109 | hp1 | a0003 | c0005 | t0003 | g0196 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0050 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0049 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0226 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0001 | g0225 | REF | REF | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0208 | REF | REF | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:67717979
|
C | T | 1 | a0007 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.32C>T | p.Ser11Phe | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/18 | 44/2844 | 32/2160 | 11/719 | chr17 | 67717979 | ||
chr17:67721409
|
T | C | 2 | a0002a0008 | 56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
missense_variant | MODERATE | c.344T>C | p.Val115Ala | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/18 | 356/2844 | 344/2160 | 115/719 | chr17 | 67721409 | ||
chr17:67721493
|
T | C | 1 | a0011 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.428T>C | p.Ile143Thr | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/18 | 440/2844 | 428/2160 | 143/719 | chr17 | 67721493 | ||
chr17:67722626
|
A | C | 1 | a0006 | 2 | HG02723.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.508A>C | p.Ile170Leu | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/18 | 520/2844 | 508/2160 | 170/719 | chr17 | 67722626 | ||
chr17:67724164
|
A | G | 1 | a0010 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.635A>G | p.Asp212Gly | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/18 | 647/2844 | 635/2160 | 212/719 | chr17 | 67724164 | ||
chr17:67726574
|
G | A | 1 | a0004 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.779G>A | p.Arg260Gln | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/18 | 791/2844 | 779/2160 | 260/719 | chr17 | 67726574 | ||
chr17:67726588
|
C | G | 1 | a0003 | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
missense_variant | MODERATE | c.793C>G | p.Leu265Val | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/18 | 805/2844 | 793/2160 | 265/719 | chr17 | 67726588 | ||
chr17:67738142
|
A | C | 1 | a0008 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1550A>C | p.Gln517Pro | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/18 | 1562/2844 | 1550/2160 | 517/719 | chr17 | 67738142 | ||
chr17:67738162
|
G | C | 1 | a0005 | 2 | NA18964.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.1570G>C | p.Glu524Gln | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/18 | 1582/2844 | 1570/2160 | 524/719 | chr17 | 67738162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:67718013
|
C | T | 1 | a0001c0009 | 2 | NA18940.hp1 NA19086.hp2 |
synonymous_variant | LOW | c.66C>T | p.Leu22Leu | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/18 | 78/2844 | 66/2160 | 22/719 | chr17 | 67718013 | ||
chr17:67722634
|
A | G | 1 | a0003c0005 | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
synonymous_variant | LOW | c.516A>G | p.Glu172Glu | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/18 | 528/2844 | 516/2160 | 172/719 | chr17 | 67722634 | ||
chr17:67724108
|
A | G | 1 | a0001c0018 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.579A>G | p.Thr193Thr | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/18 | 591/2844 | 579/2160 | 193/719 | chr17 | 67724108 | ||
chr17:67735977
|
A | G | 1 | a0001c0004 | 40 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(37): Show |
synonymous_variant | LOW | c.1008A>G | p.Ser336Ser | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/18 | 1020/2844 | 1008/2160 | 336/719 | chr17 | 67735977 | ||
chr17:67735980
|
A | T | 1 | a0001c0016 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1011A>T | p.Ser337Ser | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/18 | 1023/2844 | 1011/2160 | 337/719 | chr17 | 67735980 | ||
chr17:67738233
|
A | G | 1 | a0001c0014 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1641A>G | p.Gln547Gln | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/18 | 1653/2844 | 1641/2160 | 547/719 | chr17 | 67738233 | ||
chr17:67738938
|
A | G | 1 | a0004c0012 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1770A>G | p.Ala590Ala | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/18 | 1782/2844 | 1770/2160 | 590/719 | chr17 | 67738938 | ||
chr17:67738959
|
C | T | 1 | a0001c0013 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1791C>T | p.Ser597Ser | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/18 | 1803/2844 | 1791/2160 | 597/719 | chr17 | 67738959 | ||
chr17:67743511
|
A | G | 10 | a0001c0001a0001c0009a0001c0014others(7): Show | 168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
synonymous_variant | LOW | c.1968A>G | p.Ala656Ala | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/18 | 1980/2844 | 1968/2160 | 656/719 | chr17 | 67743511 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:67743911
|
C | T | 2 | a0004c0006t0005a0004c0012t0005 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*52C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 52 | chr17 | 67743911 | |||||
chr17:67744009
|
C | T | 1 | a0001c0004t0004 | 6 | NA18947.hp2 NA18950.hp2 NA18957.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*150C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 150 | chr17 | 67744009 | |||||
chr17:67744138
|
A | C | 1 | a0001c0002t0010 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*279A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 279 | chr17 | 67744138 | |||||
chr17:67744246
|
T | C | 3 | a0001c0002t0003a0001c0002t0010a0003c0005t0003 | 16 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*387T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 387 | chr17 | 67744246 | |||||
chr17:67744375
|
A | G | 1 | a0002c0003t0009 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 516 | chr17 | 67744375 | |||||
chr17:67744403
|
G | T | 1 | a0001c0002t0008 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 544 | chr17 | 67744403 | |||||
chr17:67744470
|
G | A | 1 | a0001c0001t0006 | 2 | NA18945.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*611G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 611 | chr17 | 67744470 | |||||
chr17:67744503
|
G | T | 25 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(22): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*644G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 644 | chr17 | 67744503 | |||||
chr17:67744512
|
A | C | 1 | a0001c0001t0007 | 2 | NA18969.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*653A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 653 | chr17 | 67744512 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:67718116
|
C | G | 38 | a0001c0001t0001g0228a0001c0002t0001g0014a0001c0002t0001g0214others(35): Show | 51 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.141+28C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718116 | ||||||
chr17:67718243
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.141+155G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718243 | ||||||
chr17:67718389
|
C | T | 1 | a0002c0003t0001g0198 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.141+301C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718389 | ||||||
chr17:67718453
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0006g0053a0001c0001t0006g0054 | 3 | HG00741.hp2 NA18945.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.141+365G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718453 | ||||||
chr17:67718467
|
C | G | 1 | a0001c0002t0002g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.141+379C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718467 | ||||||
chr17:67718474
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.141+386G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718474 | ||||||
chr17:67718524
|
G | A | 38 | a0001c0001t0001g0228a0001c0002t0001g0014a0001c0002t0001g0214others(35): Show | 51 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.141+436G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718524 | ||||||
chr17:67718562
|
G | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0191a0001c0002t0001g0192others(6): Show | 17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+474G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718562 | ||||||
chr17:67718616
|
G | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.141+528G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718616 | ||||||
chr17:67718622
|
A | G | 1 | a0001c0002t0001g0188 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.141+534A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718622 | ||||||
chr17:67718810
|
G | C | 1 | a0001c0004t0001g0211 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+722G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718810 | ||||||
chr17:67719031
|
A | G | 28 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(25): Show | 56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-643A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719031 | ||||||
chr17:67719048
|
A | C | 4 | a0001c0002t0001g0019a0001c0002t0001g0168a0001c0002t0001g0169others(1): Show | 6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-626A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719048 | ||||||
chr17:67719057
|
C | T | 2 | a0004c0006t0005g0018a0004c0012t0005g0018 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.142-617C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719057 | ||||||
chr17:67719063
|
T | C | 1 | a0001c0002t0002g0199 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.142-611T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719063 | ||||||
chr17:67719071
|
T | C | 1 | a0001c0004t0001g0212 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.142-603T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719071 | ||||||
chr17:67719112
|
G | A | 2 | a0001c0004t0001g0027a0001c0004t0001g0213 | 4 | HG00280.hp1 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-562G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719112 | ||||||
chr17:67719165
|
C | T | 7 | a0001c0002t0001g0192a0001c0002t0008g0195a0003c0005t0003g0012others(4): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-509C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719165 | ||||||
chr17:67719266
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0191 | 5 | HG02647.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-408A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719266 | ||||||
chr17:67719325
|
A | G | 28 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(25): Show | 56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-349A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719325 | ||||||
chr17:67719333
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.142-341C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719333 | ||||||
chr17:67719407
|
C | A | 3 | a0001c0001t0001g0055a0001c0001t0006g0053a0001c0001t0006g0054 | 3 | HG00741.hp2 NA18945.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.142-267C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719407 | ||||||
chr17:67720107
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.312+145A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720107 | ||||||
chr17:67720157
|
A | G | 1 | a0003c0005t0003g0196 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.312+195A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720157 | ||||||
chr17:67720161
|
G | C | 50 | a0001c0002t0001g0014a0001c0002t0001g0192a0001c0002t0001g0214others(47): Show | 88 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.312+199G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720161 | ||||||
chr17:67720184
|
T | C | 1 | a0001c0002t0002g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312+222T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720184 | ||||||
chr17:67720300
|
C | CT | 29 | a0001c0001t0001g0164a0001c0002t0001g0165a0002c0003t0001g0002others(26): Show | 57 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.312+356dupT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 67720300 | |||||
chr17:67720300
|
CT | C | 18 | a0001c0001t0001g0074a0001c0002t0001g0075a0001c0002t0001g0076others(15): Show | 21 | HG01069.hp1 HG01346.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.312+356delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 67720300 | |||||
chr17:67720387
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.312+425C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720387 | ||||||
chr17:67720415
|
C | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 171 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.312+453C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720415 | ||||||
chr17:67720432
|
G | A | 22 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0039others(19): Show | 38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.312+470G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720432 | ||||||
chr17:67720581
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.312+619A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720581 | ||||||
chr17:67720652
|
A | G | 2 | a0001c0002t0001g0192a0001c0002t0008g0195 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312+690A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720652 | ||||||
chr17:67720709
|
T | G | 1 | a0001c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.313-669T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720709 | ||||||
chr17:67720760
|
A | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.313-618A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720760 | ||||||
chr17:67720974
|
T | C | 31 | a0001c0001t0001g0228a0001c0004t0001g0007a0001c0004t0001g0027others(28): Show | 40 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.313-404T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720974 | ||||||
chr17:67721016
|
G | A | 7 | a0001c0002t0001g0192a0001c0002t0008g0195a0003c0005t0003g0012others(4): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-362G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67721016 | ||||||
chr17:67721067
|
G | A | 1 | a0001c0004t0001g0217 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.313-311G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67721067 | ||||||
chr17:67721345
|
G | A | 2 | a0004c0006t0005g0018a0004c0012t0005g0018 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.313-33G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67721345 | ||||||
chr17:67721557
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.461+31C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721557 | ||||||
chr17:67721709
|
A | G | 7 | a0001c0002t0001g0076a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.461+183A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721709 | ||||||
chr17:67721753
|
A | G | 2 | a0001c0002t0001g0038a0001c0002t0001g0075 | 3 | HG03041.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.461+227A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721753 | ||||||
chr17:67721758
|
G | A | 1 | a0001c0002t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.461+232G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721758 | ||||||
chr17:67721888
|
C | G | 52 | a0001c0002t0001g0014a0001c0002t0001g0192a0001c0002t0001g0214others(49): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.461+362C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721888 | ||||||
chr17:67721940
|
G | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG01192.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.461+414G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721940 | ||||||
chr17:67722002
|
T | TA | 9 | a0001c0002t0001g0192a0001c0002t0003g0050a0001c0002t0008g0195others(6): Show | 14 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.461+477dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr17 | 67722002 | |||||
chr17:67722026
|
G | C | 1 | a0002c0003t0001g0173 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.461+500G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722026 | ||||||
chr17:67722075
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.462-505G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722075 | ||||||
chr17:67722094
|
A | G | 1 | a0002c0003t0001g0187 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.462-486A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722094 | ||||||
chr17:67722177
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.462-403T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722177 | ||||||
chr17:67722186
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.462-394A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722186 | ||||||
chr17:67722264
|
G | A | 2 | a0001c0002t0003g0050a0001c0002t0010g0050 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.462-316G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722264 | ||||||
chr17:67722376
|
A | G | 6 | a0001c0004t0004g0235a0001c0004t0004g0236a0001c0004t0004g0237others(3): Show | 6 | NA18947.hp2 NA18950.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.462-204A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722376 | ||||||
chr17:67722431
|
A | G | 2 | a0001c0002t0002g0066a0001c0002t0002g0067 | 2 | HG01346.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.462-149A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722431 | ||||||
chr17:67722442
|
C | T | 7 | a0001c0002t0001g0076a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.462-138C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722442 | ||||||
chr17:67722682
|
TA | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.519+57delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67722682 | |||||
chr17:67722694
|
A | T | 1 | a0001c0002t0001g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.519+57A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722694 | ||||||
chr17:67722723
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.519+86C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722723 | ||||||
chr17:67722751
|
G | A | 22 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0039others(19): Show | 38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.519+114G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722751 | ||||||
chr17:67722758
|
C | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.519+121C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722758 | ||||||
chr17:67722818
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.519+181C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722818 | ||||||
chr17:67722892
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.519+255A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722892 | ||||||
chr17:67723005
|
C | CT | 11 | a0001c0002t0002g0015a0001c0002t0002g0057a0001c0002t0002g0059others(8): Show | 13 | HG01346.hp1 HG02258.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+392dupT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723005 | |||||
chr17:67723005
|
CT | C | 31 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0069others(28): Show | 62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.519+392delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723005 | |||||
chr17:67723005
|
CTTTTTTT | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.519+386_519+392del others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723005 | |||||
chr17:67723076
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.519+439G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723076 | ||||||
chr17:67723103
|
C | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.519+466C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723103 | ||||||
chr17:67723114
|
G | A | 2 | a0001c0002t0001g0014a0001c0002t0001g0214 | 5 | NA18963.hp2 NA18990.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+477G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723114 | ||||||
chr17:67723127
|
C | T | 1 | a0001c0004t0001g0141 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.519+490C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723127 | ||||||
chr17:67723138
|
G | A | 49 | a0001c0002t0001g0014a0001c0002t0001g0192a0001c0002t0001g0214others(46): Show | 87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.519+501G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723138 | ||||||
chr17:67723156
|
G | A | 3 | a0001c0002t0002g0059a0001c0002t0002g0066a0001c0002t0002g0067 | 3 | HG01346.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.519+519G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723156 | ||||||
chr17:67723238
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+601C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723238 | ||||||
chr17:67723287
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.519+650C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723287 | ||||||
chr17:67723307
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.519+670T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723307 | ||||||
chr17:67723310
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519+673C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723310 | ||||||
chr17:67723347
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.520-702G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723347 | ||||||
chr17:67723370
|
A | ATTTTTTT others(4): Show |
1 | a0001c0002t0002g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.520-652_520-642dup others(11): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
AT | A | 9 | a0001c0002t0002g0013a0001c0002t0002g0061a0001c0002t0002g0062others(6): Show | 12 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-642delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATT | A | 4 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0058others(1): Show | 6 | HG00735.hp2 HG01255.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-643_520-642del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTT | A | 13 | a0001c0001t0001g0228a0001c0002t0001g0168a0001c0002t0001g0169others(10): Show | 15 | HG00609.hp2 HG00621.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.520-646_520-642del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTT | A | 17 | a0001c0002t0001g0159a0001c0002t0001g0162a0001c0004t0001g0007others(14): Show | 24 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.520-647_520-642del others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT | A | 8 | a0001c0001t0001g0139a0001c0002t0001g0156a0001c0002t0001g0157others(5): Show | 8 | HG01358.hp2 HG02451.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-648_520-642del others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(1): Show |
A | 33 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0079others(30): Show | 51 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.520-649_520-642del others(8): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(2): Show |
A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 145 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.520-650_520-642del others(9): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(3): Show |
A | 10 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0030others(7): Show | 15 | HG01071.hp1 HG01517.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-651_520-642del others(10): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0002t0002g0201a0003c0005t0003g0194 | 2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.520-653_520-642del others(12): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(6): Show |
A | 8 | a0002c0003t0001g0044a0002c0003t0001g0173a0002c0003t0001g0186others(5): Show | 14 | HG00597.hp2 HG01109.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-654_520-642del others(13): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(7): Show |
A | 20 | a0002c0003t0001g0002a0002c0003t0001g0021a0002c0003t0001g0022others(17): Show | 46 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.520-655_520-642del others(14): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(8): Show |
A | 6 | a0001c0002t0001g0014a0001c0002t0001g0214a0002c0003t0001g0020others(3): Show | 10 | NA18946.hp1 NA18962.hp2 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-656_520-642del others(15): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0002t0003g0049 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.520-657_520-642del others(16): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(10): Show |
A | 4 | a0001c0002t0003g0050a0001c0002t0003g0215a0001c0002t0003g0216others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-658_520-642del others(17): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(12): Show |
A | 3 | a0001c0002t0001g0076a0001c0002t0001g0160a0001c0002t0001g0165 | 3 | HG02486.hp2 HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.520-660_520-642del others(19): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723370
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0002t0001g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.520-661_520-642del others(20): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | |||||
chr17:67723413
|
G | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.520-636G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723413 | ||||||
chr17:67723435
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.520-614T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723435 | ||||||
chr17:67723544
|
A | G | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-505A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723544 | ||||||
chr17:67723608
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.520-441C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723608 | ||||||
chr17:67723632
|
C | T | 2 | a0001c0002t0001g0192a0001c0002t0008g0195 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.520-417C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723632 | ||||||
chr17:67723662
|
C | T | 3 | a0001c0004t0001g0217a0001c0004t0001g0233a0001c0004t0001g0234 | 3 | NA18979.hp1 NA18981.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.520-387C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723662 | ||||||
chr17:67723740
|
C | G | 2 | a0001c0002t0001g0192a0001c0002t0008g0195 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.520-309C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723740 | ||||||
chr17:67723744
|
T | TA | 33 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0039others(30): Show | 51 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.520-292dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723744 | |||||
chr17:67723744
|
TA | T | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-292delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723744 | |||||
chr17:67723847
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0129 | 3 | NA18948.hp2 NA18953.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.520-202A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723847 | ||||||
chr17:67723848
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.520-201A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723848 | ||||||
chr17:67723892
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.520-157C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723892 | ||||||
chr17:67723915
|
A | C | 1 | a0001c0002t0003g0049 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.520-134A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723915 | ||||||
chr17:67723932
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.520-117A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723932 | ||||||
chr17:67723982
|
T | C | 2 | a0001c0002t0001g0076a0001c0002t0001g0160 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.520-67T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723982 | ||||||
chr17:67724034
|
C | CT | 13 | a0001c0001t0001g0081a0001c0001t0001g0128a0001c0001t0001g0166others(10): Show | 14 | HG01099.hp1 HG01496.hp1 HG02258.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.520-5dupT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67724034 | |||||
chr17:67724034
|
CT | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.520-5delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67724034 | |||||
chr17:67724224
|
T | A | 1 | a0003c0005t0003g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664+31T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724224 | ||||||
chr17:67724230
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 164 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.664+37A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724230 | ||||||
chr17:67724244
|
T | C | 1 | a0007c0019t0001g0068 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.664+51T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724244 | ||||||
chr17:67724328
|
T | C | 1 | a0002c0003t0001g0176 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.664+135T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724328 | ||||||
chr17:67724332
|
CT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 293 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.664+158delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr17 | 67724332 | |||||
chr17:67724332
|
CTT | C | 14 | a0001c0001t0001g0092a0001c0002t0001g0014a0001c0002t0001g0076others(11): Show | 23 | HG01109.hp1 HG01168.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.664+157_664+158del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr17 | 67724332 | |||||
chr17:67724364
|
C | T | 2 | a0001c0002t0001g0014a0001c0002t0001g0214 | 5 | NA18963.hp2 NA18990.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+171C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724364 | ||||||
chr17:67724436
|
C | T | 1 | a0007c0019t0001g0068 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.664+243C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724436 | ||||||
chr17:67724438
|
A | G | 1 | a0001c0002t0001g0019 | 3 | NA18944.hp2 NA18947.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.664+245A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724438 | ||||||
chr17:67724468
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.664+275G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724468 | ||||||
chr17:67724480
|
C | T | 1 | a0003c0005t0003g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.664+287C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724480 | ||||||
chr17:67724596
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.664+403C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724596 | ||||||
chr17:67724627
|
C | G | 2 | a0006c0008t0001g0124a0006c0008t0001g0125 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.664+434C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724627 | ||||||
chr17:67724628
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.664+435G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724628 | ||||||
chr17:67724664
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 171 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.664+471G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724664 | ||||||
chr17:67724718
|
A | C | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+525A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724718 | ||||||
chr17:67724788
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.664+595A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724788 | ||||||
chr17:67724829
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.664+636T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724829 | ||||||
chr17:67724834
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.664+641A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724834 | ||||||
chr17:67724873
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.664+680A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724873 | ||||||
chr17:67724927
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.664+734G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724927 | ||||||
chr17:67724990
|
G | A | 12 | a0001c0002t0002g0015a0001c0002t0002g0057a0001c0002t0002g0058others(9): Show | 14 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.664+797G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724990 | ||||||
chr17:67725013
|
G | A | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.664+820G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725013 | ||||||
chr17:67725052
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664+859G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725052 | ||||||
chr17:67725059
|
G | A | 1 | a0001c0002t0001g0039 | 2 | HG00642.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.664+866G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725059 | ||||||
chr17:67725068
|
A | G | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+875A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725068 | ||||||
chr17:67725090
|
A | G | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+897A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725090 | ||||||
chr17:67725137
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.664+944T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725137 | ||||||
chr17:67725174
|
T | C | 3 | a0002c0003t0001g0021a0002c0003t0001g0175a0002c0003t0001g0186 | 5 | NA18943.hp2 NA18961.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+981T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725174 | ||||||
chr17:67725193
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.664+1000T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725193 | ||||||
chr17:67725331
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.665-1129A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725331 | ||||||
chr17:67725449
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.665-1011C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725449 | ||||||
chr17:67725779
|
G | A | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665-681G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725779 | ||||||
chr17:67725780
|
G | A | 1 | a0001c0002t0003g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.665-680G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725780 | ||||||
chr17:67725830
|
G | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0214a0007c0019t0001g0068 | 6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-630G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725830 | ||||||
chr17:67725845
|
C | G | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-615C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725845 | ||||||
chr17:67725881
|
A | C | 3 | a0001c0002t0001g0014a0001c0002t0001g0214a0007c0019t0001g0068 | 6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-579A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725881 | ||||||
chr17:67726187
|
G | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.665-273G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67726187 | ||||||
chr17:67726258
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.665-202T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67726258 | ||||||
chr17:67726281
|
C | T | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-179C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67726281 | ||||||
chr17:67726696
|
C | T | 2 | a0004c0006t0005g0018a0004c0012t0005g0018 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.853+48C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726696 | ||||||
chr17:67726733
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.853+85G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726733 | ||||||
chr17:67726775
|
A | G | 1 | a0001c0001t0001g0011 | 4 | HG02647.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+127A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726775 | ||||||
chr17:67726865
|
A | G | 3 | a0001c0002t0001g0014a0001c0002t0001g0214a0007c0019t0001g0068 | 6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+217A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726865 | ||||||
chr17:67726900
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.853+252C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726900 | ||||||
chr17:67727137
|
A | G | 1 | a0002c0003t0001g0184 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.853+489A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727137 | ||||||
chr17:67727310
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.853+662A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727310 | ||||||
chr17:67727595
|
C | T | 2 | a0001c0002t0001g0042a0001c0002t0002g0072 | 3 | HG01361.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.853+947C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727595 | ||||||
chr17:67727604
|
C | T | 47 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0015others(44): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+956C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727604 | ||||||
chr17:67727644
|
C | T | 2 | a0001c0002t0001g0146a0001c0002t0001g0153 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.853+996C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727644 | ||||||
chr17:67727645
|
G | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0214a0007c0019t0001g0068 | 6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+997G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727645 | ||||||
chr17:67727653
|
G | A | 4 | a0001c0002t0002g0060a0001c0002t0002g0061a0001c0002t0002g0063others(1): Show | 4 | HG02258.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+1005G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727653 | ||||||
chr17:67727657
|
C | CA | 5 | a0001c0002t0002g0066a0001c0002t0002g0067a0002c0003t0001g0173others(2): Show | 6 | HG01346.hp1 HG01884.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+1021dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727657 | |||||
chr17:67727657
|
CA | C | 7 | a0001c0001t0001g0121a0002c0003t0001g0183a0003c0005t0003g0012others(4): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+1021delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727657 | |||||
chr17:67727759
|
T | G | 47 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0015others(44): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1111T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727759 | ||||||
chr17:67727761
|
C | T | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.853+1113C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727761 | ||||||
chr17:67727793
|
A | G | 47 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0015others(44): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1145A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727793 | ||||||
chr17:67727842
|
A | G | 47 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0015others(44): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1194A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727842 | ||||||
chr17:67727918
|
CA | C | 22 | a0001c0002t0002g0013a0001c0002t0002g0026a0001c0002t0002g0028others(19): Show | 31 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.853+1295delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | |||||
chr17:67727918
|
CAAA | C | 8 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(5): Show | 12 | HG00544.hp1 HG00621.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+1293_853+1295d others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | |||||
chr17:67727918
|
CAAAA | C | 42 | a0001c0002t0001g0147a0001c0002t0001g0159a0001c0002t0001g0160others(39): Show | 69 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.853+1292_853+1295d others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | |||||
chr17:67727918
|
CAAAAA | C | 37 | a0001c0001t0001g0095a0001c0001t0001g0130a0001c0001t0001g0138others(34): Show | 61 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.853+1291_853+1295d others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | |||||
chr17:67727918
|
CAAAAAA | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(56): Show | 106 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.853+1290_853+1295d others(8): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | |||||
chr17:67727918
|
CAAAAAAA | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.853+1289_853+1295d others(9): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | |||||
chr17:67727918
|
CAAAAAAA others(7): Show |
C | 6 | a0001c0002t0001g0019a0001c0002t0001g0168a0001c0002t0001g0169others(3): Show | 9 | HG00609.hp2 HG01884.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+1282_853+1295d others(16): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | |||||
chr17:67727937
|
A | C | 27 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(24): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.853+1289A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727937 | ||||||
chr17:67727982
|
C | T | 6 | a0001c0002t0001g0010a0001c0002t0001g0151a0001c0002t0001g0152others(3): Show | 9 | NA18943.hp1 NA18949.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+1334C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727982 | ||||||
chr17:67728043
|
A | G | 1 | a0001c0002t0001g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.853+1395A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728043 | ||||||
chr17:67728076
|
T | C | 50 | a0001c0001t0001g0096a0001c0002t0001g0014a0001c0002t0001g0038others(47): Show | 89 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.853+1428T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728076 | ||||||
chr17:67728093
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.853+1445C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728093 | ||||||
chr17:67728175
|
G | A | 3 | a0002c0003t0001g0023a0002c0003t0001g0174a0002c0003t0001g0177 | 5 | NA18971.hp1 NA19001.hp1 NA19075.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+1527G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728175 | ||||||
chr17:67728196
|
C | G | 2 | a0001c0002t0002g0057a0001c0002t0002g0065 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.853+1548C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728196 | ||||||
chr17:67728328
|
A | G | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+1680A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728328 | ||||||
chr17:67728469
|
G | A | 47 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0015others(44): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1821G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728469 | ||||||
chr17:67728685
|
G | A | 1 | a0006c0008t0001g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.853+2037G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728685 | ||||||
chr17:67728918
|
C | T | 2 | a0001c0002t0003g0050a0001c0002t0010g0050 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.853+2270C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728918 | ||||||
chr17:67728950
|
G | T | 47 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0015others(44): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+2302G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728950 | ||||||
chr17:67729099
|
TG | T | 40 | a0001c0002t0001g0014a0001c0002t0001g0214a0001c0002t0002g0015others(37): Show | 73 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.853+2452delG | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729099 | ||||||
chr17:67729100
|
G | T | 7 | a0002c0003t0001g0173a0002c0003t0001g0183a0003c0005t0003g0012others(4): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+2452G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729100 | ||||||
chr17:67729100
|
GT | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.853+2463delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67729100 | |||||
chr17:67729104
|
T | G | 7 | a0001c0002t0001g0038a0001c0002t0001g0075a0001c0002t0003g0215others(4): Show | 8 | HG00408.hp1 HG02071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+2456T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729104 | ||||||
chr17:67729155
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.853+2507C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729155 | ||||||
chr17:67729245
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0110others(2): Show | 10 | HG00642.hp2 HG01069.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.853+2597C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729245 | ||||||
chr17:67729398
|
C | T | 5 | a0001c0004t0001g0141a0001c0004t0001g0217a0001c0004t0001g0227others(2): Show | 5 | NA18979.hp1 NA18981.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+2750C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729398 | ||||||
chr17:67729584
|
CT | C | 7 | a0001c0002t0003g0215a0001c0002t0003g0216a0003c0005t0003g0012others(4): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+2948delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67729584 | |||||
chr17:67729639
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.853+2991C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729639 | ||||||
chr17:67729648
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.853+3000G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729648 | ||||||
chr17:67729671
|
C | T | 2 | a0001c0002t0002g0066a0001c0002t0002g0067 | 2 | HG01346.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.853+3023C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729671 | ||||||
chr17:67729672
|
G | A | 28 | a0001c0002t0001g0147a0002c0003t0001g0002a0002c0003t0001g0020others(25): Show | 56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.853+3024G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729672 | ||||||
chr17:67729673
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853+3025G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729673 | ||||||
chr17:67729723
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0122 | 3 | HG01361.hp1 HG01433.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.853+3075C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729723 | ||||||
chr17:67729831
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0113others(1): Show | 7 | HG00423.hp1 HG00609.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.853+3183G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729831 | ||||||
chr17:67729961
|
C | G | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.853+3313C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729961 | ||||||
chr17:67729988
|
C | T | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.853+3340C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729988 | ||||||
chr17:67730090
|
A | G | 1 | a0001c0002t0001g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.853+3442A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730090 | ||||||
chr17:67730139
|
G | A | 22 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0039others(19): Show | 38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.853+3491G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730139 | ||||||
chr17:67730141
|
T | C | 22 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0039others(19): Show | 38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.853+3493T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730141 | ||||||
chr17:67730205
|
A | G | 2 | a0001c0002t0003g0050a0001c0002t0010g0050 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.853+3557A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730205 | ||||||
chr17:67730214
|
C | A | 27 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(24): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.853+3566C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730214 | ||||||
chr17:67730252
|
TTTTG | T | 4 | a0001c0001t0001g0087a0001c0002t0001g0014a0001c0002t0001g0214others(1): Show | 7 | HG02257.hp1 HG02970.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+3620_853+3623d others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67730252 | |||||
chr17:67730268
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0191 | 5 | HG02647.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.853+3620G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730268 | ||||||
chr17:67730353
|
C | T | 1 | a0001c0002t0001g0041 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.853+3705C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730353 | ||||||
chr17:67730552
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.854-3811G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730552 | ||||||
chr17:67730642
|
AT | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.854-3714delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67730642 | |||||
chr17:67730734
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.854-3629G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730734 | ||||||
chr17:67730760
|
C | T | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-3603C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730760 | ||||||
chr17:67730812
|
C | T | 27 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(24): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.854-3551C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730812 | ||||||
chr17:67731084
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.854-3279T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731084 | ||||||
chr17:67731238
|
TTCGTGCA others(269): Show |
T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.854-3107_854-2832d others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731238 | |||||
chr17:67731251
|
GT | G | 12 | a0001c0002t0002g0013a0001c0002t0002g0045a0001c0002t0002g0048others(9): Show | 17 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.854-3082delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731251 | |||||
chr17:67731251
|
GTT | G | 6 | a0001c0002t0002g0060a0001c0002t0002g0062a0001c0002t0002g0064others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-3083_854-3082d others(4): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731251 | |||||
chr17:67731251
|
GTTT | G | 7 | a0001c0002t0002g0015a0001c0002t0002g0058a0001c0002t0002g0059others(4): Show | 9 | HG01346.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.854-3084_854-3082d others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731251 | |||||
chr17:67731260
|
T | G | 2 | a0001c0002t0002g0066a0001c0002t0002g0067 | 2 | HG01346.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.854-3103T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731260 | ||||||
chr17:67731598
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.854-2765C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731598 | ||||||
chr17:67731633
|
C | T | 1 | a0002c0003t0001g0182 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.854-2730C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731633 | ||||||
chr17:67731751
|
G | A | 1 | a0002c0003t0001g0178 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.854-2612G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731751 | ||||||
chr17:67731826
|
A | G | 4 | a0001c0002t0001g0019a0001c0002t0001g0168a0001c0002t0001g0169others(1): Show | 6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-2537A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731826 | ||||||
chr17:67731916
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.854-2447G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731916 | ||||||
chr17:67731968
|
A | G | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0108others(2): Show | 6 | HG01358.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-2395A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731968 | ||||||
chr17:67732009
|
A | G | 1 | a0001c0004t0001g0223 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.854-2354A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732009 | ||||||
chr17:67732056
|
G | A | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-2307G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732056 | ||||||
chr17:67732146
|
A | G | 1 | a0001c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.854-2217A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732146 | ||||||
chr17:67732416
|
G | A | 17 | a0001c0002t0002g0015a0001c0002t0002g0057a0001c0002t0002g0058others(14): Show | 24 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-1947G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732416 | ||||||
chr17:67732432
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.854-1931G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732432 | ||||||
chr17:67732439
|
C | G | 4 | a0001c0002t0001g0019a0001c0002t0001g0168a0001c0002t0001g0169others(1): Show | 6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-1924C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732439 | ||||||
chr17:67732491
|
C | CA | 11 | a0001c0001t0001g0114a0001c0001t0001g0121a0001c0001t0001g0135others(8): Show | 12 | HG00597.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.854-1854dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67732491 | |||||
chr17:67732491
|
CA | C | 6 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0118others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-1854delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67732491 | |||||
chr17:67732491
|
CAA | C | 17 | a0001c0002t0002g0015a0001c0002t0002g0057a0001c0002t0002g0058others(14): Show | 24 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-1855_854-1854d others(4): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67732491 | |||||
chr17:67732573
|
A | T | 2 | a0001c0002t0003g0215a0001c0002t0003g0216 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.854-1790A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732573 | ||||||
chr17:67732641
|
T | G | 17 | a0001c0002t0002g0015a0001c0002t0002g0057a0001c0002t0002g0058others(14): Show | 24 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-1722T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732641 | ||||||
chr17:67732678
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.854-1685G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732678 | ||||||
chr17:67732781
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-1582C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732781 | ||||||
chr17:67733021
|
A | G | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-1342A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733021 | ||||||
chr17:67733049
|
G | A | 3 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0204 | 5 | HG00735.hp2 HG00738.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.854-1314G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733049 | ||||||
chr17:67733070
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.854-1293A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733070 | ||||||
chr17:67733129
|
C | T | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-1234C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733129 | ||||||
chr17:67733320
|
G | A | 33 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(30): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.854-1043G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733320 | ||||||
chr17:67733521
|
A | G | 1 | a0002c0003t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.854-842A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733521 | ||||||
chr17:67733690
|
G | T | 7 | a0001c0002t0001g0076a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.854-673G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733690 | ||||||
chr17:67733847
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.854-516T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733847 | ||||||
chr17:67733935
|
A | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.854-428A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733935 | ||||||
chr17:67733943
|
CTG | C | 2 | a0001c0002t0001g0041a0001c0002t0001g0144 | 3 | HG01099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.854-418_854-417del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67733943 | |||||
chr17:67733945
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.854-418G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733945 | ||||||
chr17:67733968
|
T | G | 5 | a0001c0002t0001g0040a0001c0002t0001g0042a0001c0002t0001g0146others(2): Show | 7 | HG01168.hp2 HG01169.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.854-395T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733968 | ||||||
chr17:67734094
|
GAAGCC | G | 24 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0014others(21): Show | 43 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.854-267_854-263del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67734094 | |||||
chr17:67734115
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.854-248T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734115 | ||||||
chr17:67734143
|
T | C | 31 | a0001c0004t0001g0007a0001c0004t0001g0027a0001c0004t0001g0051others(28): Show | 40 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.854-220T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734143 | ||||||
chr17:67734145
|
C | G | 1 | a0001c0002t0001g0156 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.854-218C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734145 | ||||||
chr17:67734145
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.854-218C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734145 | ||||||
chr17:67734288
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.854-75G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734288 | ||||||
chr17:67734542
|
T | C | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+103T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734542 | ||||||
chr17:67734640
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.930+201A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734640 | ||||||
chr17:67734731
|
A | G | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+292A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734731 | ||||||
chr17:67734755
|
A | G | 7 | a0001c0002t0001g0076a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.930+316A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734755 | ||||||
chr17:67734774
|
G | A | 1 | a0001c0002t0002g0065 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.930+335G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734774 | ||||||
chr17:67735031
|
C | G | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.930+592C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735031 | ||||||
chr17:67735068
|
GTGTTAAA | G | 2 | a0002c0003t0001g0023a0002c0003t0001g0174 | 4 | NA19001.hp1 NA19075.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+642_930+648del others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 67735068 | |||||
chr17:67735135
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.930+696A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735135 | ||||||
chr17:67735234
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931-666T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735234 | ||||||
chr17:67735332
|
TTATAC | T | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.931-566_931-562del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 67735332 | |||||
chr17:67735336
|
A | C | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.931-564A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735336 | ||||||
chr17:67735382
|
GT | G | 31 | a0001c0004t0001g0007a0001c0004t0001g0027a0001c0004t0001g0051others(28): Show | 40 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.931-517delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735382 | ||||||
chr17:67735390
|
ACT | A | 8 | a0001c0002t0001g0076a0001c0002t0001g0159a0001c0002t0001g0160others(5): Show | 8 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.931-508_931-507del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 67735390 | |||||
chr17:67735494
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.931-406C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735494 | ||||||
chr17:67735529
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.931-371T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735529 | ||||||
chr17:67735677
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.931-223A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735677 | ||||||
chr17:67735797
|
G | A | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.931-103G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735797 | ||||||
chr17:67735875
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.931-25A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735875 | ||||||
chr17:67735958
|
C | CATACAAG others(75): Show |
1 | a0009c0015t0001g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.990_1054+17dupATAC others(78): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 67735958 | |||||
chr17:67736062
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0086 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1054+39G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736062 | ||||||
chr17:67736146
|
T | C | 8 | a0001c0002t0001g0019a0001c0002t0001g0168a0001c0002t0001g0169others(5): Show | 11 | HG00609.hp2 HG01884.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.1054+123T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736146 | ||||||
chr17:67736174
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1054+151G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736174 | ||||||
chr17:67736236
|
G | A | 4 | a0001c0002t0001g0019a0001c0002t0001g0168a0001c0002t0001g0169others(1): Show | 6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+213G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736236 | ||||||
chr17:67736292
|
G | GA | 13 | a0001c0001t0001g0035a0001c0001t0001g0087a0001c0001t0001g0098others(10): Show | 14 | HG01099.hp1 HG01175.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1054+273dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 67736292 | |||||
chr17:67736296
|
AC | A | 3 | a0001c0001t0001g0111a0001c0002t0001g0192a0001c0002t0008g0195 | 3 | HG03486.hp1 HG03491.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1054+274delC | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736296 | ||||||
chr17:67736297
|
C | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1054+274C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736297 | ||||||
chr17:67736369
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1055-297G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736369 | ||||||
chr17:67736419
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1055-247A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736419 | ||||||
chr17:67736458
|
A | G | 4 | a0001c0002t0001g0019a0001c0002t0001g0168a0001c0002t0001g0169others(1): Show | 6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-208A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736458 | ||||||
chr17:67736530
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1055-136G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736530 | ||||||
chr17:67736775
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1143+21T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 10/17 | chr17 | 67736775 | ||||||
chr17:67736843
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1143+89A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 10/17 | chr17 | 67736843 | ||||||
chr17:67737003
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 160 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1144-68T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 10/17 | chr17 | 67737003 | ||||||
chr17:67737339
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1219-169T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 11/17 | chr17 | 67737339 | ||||||
chr17:67737376
|
G | A | 2 | a0004c0006t0005g0018a0004c0012t0005g0018 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1219-132G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 11/17 | chr17 | 67737376 | ||||||
chr17:67737751
|
A | G | 3 | a0001c0004t0001g0224a0001c0004t0001g0230a0001c0004t0001g0231 | 3 | HG00408.hp1 HG02071.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1403+59A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 12/17 | chr17 | 67737751 | ||||||
chr17:67738061
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1530-61G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 13/17 | chr17 | 67738061 | ||||||
chr17:67738113
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1530-9C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 13/17 | chr17 | 67738113 | ||||||
chr17:67738398
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1763+43A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738398 | ||||||
chr17:67738473
|
T | C | 1 | a0002c0003t0001g0179 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1763+118T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738473 | ||||||
chr17:67738527
|
T | G | 3 | a0001c0002t0002g0059a0001c0002t0002g0066a0001c0002t0002g0067 | 3 | HG01346.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1763+172T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738527 | ||||||
chr17:67738539
|
A | T | 1 | a0008c0010t0001g0181 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1763+184A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738539 | ||||||
chr17:67738541
|
T | A | 1 | a0008c0010t0001g0181 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1763+186T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738541 | ||||||
chr17:67738597
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1763+242C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738597 | ||||||
chr17:67738598
|
G | A | 2 | a0001c0002t0002g0058a0001c0002t0002g0062 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1763+243G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738598 | ||||||
chr17:67738678
|
TA | T | 39 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0113others(36): Show | 70 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1764-240delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr17 | 67738678 | |||||
chr17:67738712
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1764-220A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738712 | ||||||
chr17:67738722
|
T | C | 1 | a0001c0002t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1764-210T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738722 | ||||||
chr17:67738912
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0116 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1764-20G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738912 | ||||||
chr17:67739295
|
A | G | 1 | a0001c0002t0001g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1843-221A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739295 | ||||||
chr17:67739300
|
T | A | 1 | a0001c0004t0001g0227 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1843-216T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739300 | ||||||
chr17:67739405
|
G | A | 8 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0102others(5): Show | 8 | HG02523.hp2 NA18954.hp1 NA18997.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843-111G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739405 | ||||||
chr17:67739427
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0133 | 2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1843-89G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739427 | ||||||
chr17:67739430
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0133 | 2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1843-86C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739430 | ||||||
chr17:67739431
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0133 | 2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1843-85A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739431 | ||||||
chr17:67739447
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 171 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1843-69G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739447 | ||||||
chr17:67739626
|
CTTTGA | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0191 | 5 | HG02647.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+23_1935+27del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67739626 | |||||
chr17:67739681
|
C | T | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+73C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67739681 | ||||||
chr17:67739756
|
A | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0039others(19): Show | 38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1935+148A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67739756 | ||||||
chr17:67739905
|
C | T | 12 | a0001c0002t0002g0015a0001c0002t0002g0057a0001c0002t0002g0058others(9): Show | 14 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1935+297C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67739905 | ||||||
chr17:67740102
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0123 | 3 | HG02132.hp1 HG02523.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1935+494G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740102 | ||||||
chr17:67740192
|
G | A | 1 | a0002c0003t0001g0180 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1935+584G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740192 | ||||||
chr17:67740233
|
CA | C | 18 | a0001c0002t0001g0038a0001c0002t0001g0075a0001c0002t0002g0015others(15): Show | 26 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1935+636delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740233 | |||||
chr17:67740247
|
G | A | 2 | a0001c0002t0001g0192a0001c0002t0008g0195 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1935+639G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740247 | ||||||
chr17:67740333
|
G | C | 28 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(25): Show | 56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1935+725G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740333 | ||||||
chr17:67740443
|
C | T | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+835C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740443 | ||||||
chr17:67740530
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1935+922A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740530 | ||||||
chr17:67740534
|
G | A | 2 | a0004c0006t0005g0018a0004c0012t0005g0018 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1935+926G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740534 | ||||||
chr17:67740609
|
C | CA | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1935+1016dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740609 | |||||
chr17:67740609
|
C | CAA | 9 | a0001c0001t0001g0074a0001c0001t0001g0079a0001c0001t0001g0084others(6): Show | 9 | HG01069.hp1 HG01891.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1935+1015_1935+101 others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740609 | |||||
chr17:67740609
|
CA | C | 28 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(25): Show | 56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1935+1016delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740609 | |||||
chr17:67740696
|
C | T | 1 | a0001c0002t0002g0204 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1935+1088C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740696 | ||||||
chr17:67740796
|
A | G | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1935+1188A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740796 | ||||||
chr17:67740797
|
T | C | 31 | a0001c0004t0001g0007a0001c0004t0001g0027a0001c0004t0001g0051others(28): Show | 40 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.1935+1189T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740797 | ||||||
chr17:67740820
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1935+1212T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740820 | ||||||
chr17:67740900
|
CT | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1935+1303delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740900 | |||||
chr17:67741101
|
G | A | 31 | a0001c0002t0001g0014a0001c0002t0001g0214a0002c0003t0001g0002others(28): Show | 62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1935+1493G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741101 | ||||||
chr17:67741103
|
T | C | 5 | a0001c0002t0003g0049a0001c0002t0003g0050a0001c0002t0003g0215others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1935+1495T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741103 | ||||||
chr17:67741133
|
G | A | 2 | a0001c0002t0001g0161a0001c0002t0001g0162 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1935+1525G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741133 | ||||||
chr17:67741152
|
C | G | 1 | a0003c0005t0003g0025 | 3 | HG01109.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1935+1544C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741152 | ||||||
chr17:67741156
|
G | A | 2 | a0001c0002t0001g0192a0001c0002t0008g0195 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1935+1548G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741156 | ||||||
chr17:67741270
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1935+1662G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741270 | ||||||
chr17:67741282
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1935+1674C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741282 | ||||||
chr17:67741288
|
T | C | 5 | a0003c0005t0003g0012a0003c0005t0003g0025a0003c0005t0003g0193others(2): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+1680T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741288 | ||||||
chr17:67741588
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1936-1891C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741588 | ||||||
chr17:67741686
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(40): Show | 73 | HG00438.hp1 HG00642.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1936-1793C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741686 | ||||||
chr17:67741753
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1936-1726G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741753 | ||||||
chr17:67741909
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1936-1570C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741909 | ||||||
chr17:67742216
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1936-1263T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742216 | ||||||
chr17:67742444
|
C | G | 1 | a0001c0002t0003g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1936-1035C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742444 | ||||||
chr17:67742657
|
G | A | 21 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0039others(18): Show | 37 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1936-822G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742657 | ||||||
chr17:67742823
|
A | C | 1 | a0001c0002t0002g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1936-656A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742823 | ||||||
chr17:67742961
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1936-518T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742961 | ||||||
chr17:67742968
|
G | A | 7 | a0001c0002t0001g0076a0001c0002t0001g0159a0001c0002t0001g0160others(4): Show | 7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1936-511G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742968 | ||||||
chr17:67743109
|
G | A | 1 | a0001c0002t0003g0049 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1936-370G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743109 | ||||||
chr17:67743113
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1936-366A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743113 | ||||||
chr17:67743163
|
G | A | 2 | a0002c0003t0001g0022a0002c0003t0001g0024 | 6 | HG00423.hp2 HG00673.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-316G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743163 | ||||||
chr17:67743312
|
G | A | 27 | a0002c0003t0001g0002a0002c0003t0001g0020a0002c0003t0001g0021others(24): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1936-167G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743312 | ||||||
chr17:67743673
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.2044-70A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/17 | chr17 | 67743673 | ||||||
chr17:67743680
|
C | G | 8 | a0001c0002t0001g0076a0001c0002t0001g0159a0001c0002t0001g0160others(5): Show | 8 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2044-63C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/17 | chr17 | 67743680 | ||||||
chr17:67743681
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2044-62A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/17 | chr17 | 67743681 |