geneid | 51667 |
---|---|
ensemblid | ENSG00000013374.17 |
hgncid | 17623 |
symbol | NUB1 |
name | negative regulator of ubiquitin like proteins 1 |
refseq_nuc | NM_001243351.2 |
refseq_prot | NP_001230280.2 |
ensembl_nuc | ENST00000568733.6 |
ensembl_prot | ENSP00000454264.2 |
mane_status | MANE Select |
chr | chr7 |
start | 151341812 |
end | 151378449 |
strand | + |
ver | v1.2 |
region | chr7:151341812-151378449 |
region5000 | chr7:151336812-151383449 |
regionname0 | NUB1_chr7_151341812_151378449 |
regionname5000 | NUB1_chr7_151336812_151383449 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 615 | 406 | 94 | 76 | 169 | 16 | 49 | 132 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0002 | 0/0 | 615 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0003 | 0/0 | 615 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0004 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0005 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0006 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0007 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0008 | 0/0 | 615 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0009 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0010 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0011 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1848 | 258 | 81 | 46 | 82 | 9 | 39 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0002 | 0/1 | 1848 | 120 | 8 | 25 | 73 | 5 | 8 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0003 | 0/0 | 1848 | 15 | 3 | 4 | 5 | 2 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0004 | 0/0 | 1848 | 11 | 0 | 1 | 9 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0005 | 0/0 | 1848 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0006 | 0/0 | 1848 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0007 | 0/0 | 1848 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0008 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0009 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0010 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0011 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0012 | 0/0 | 1848 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0013 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0014 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
c0015 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1262 | 135 | 11 | 26 | 84 | 5 | 8 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0002 | 0/0 | 1262 | 103 | 10 | 31 | 59 | 2 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0003 | 1/0 | 1262 | 72 | 32 | 12 | 0 | 6 | 21 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0004 | 0/0 | 1262 | 59 | 24 | 6 | 17 | 1 | 11 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0005 | 0/0 | 1262 | 24 | 0 | 2 | 13 | 2 | 7 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0006 | 0/0 | 1262 | 10 | 10 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0007 | 0/0 | 1262 | 7 | 7 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0008 | 0/0 | 1262 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0009 | 0/0 | 1262 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0010 | 0/0 | 1262 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0011 | 0/0 | 1262 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0012 | 0/0 | 1262 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
t0013 | 0/0 | 1262 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1848 | 258 | 81 | 46 | 82 | 9 | 39 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0002 | 0/1 | 1848 | 120 | 8 | 25 | 73 | 5 | 8 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0003 | 0/0 | 1848 | 15 | 3 | 4 | 5 | 2 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0004 | 0/0 | 1848 | 11 | 0 | 1 | 9 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0005 | 0/0 | 1848 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0002c0006 | 0/0 | 1848 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0003c0007 | 0/0 | 1848 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0004c0010 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0005c0011 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0006c0014 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0007c0013 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0008c0012 | 0/0 | 1848 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0009c0015 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0010c0008 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0011c0009 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0002 | 0/0 | 3109 | 92 | 10 | 27 | 53 | 1 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0003 | 1/0 | 3109 | 67 | 28 | 12 | 0 | 6 | 20 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0004 | 0/0 | 3109 | 55 | 24 | 4 | 15 | 1 | 11 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0005 | 0/0 | 3109 | 22 | 0 | 2 | 13 | 1 | 6 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0006 | 0/0 | 3109 | 10 | 10 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0007 | 0/0 | 3109 | 6 | 6 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0008 | 0/0 | 3109 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0010 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0011 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0001t0012 | 0/0 | 3109 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0002t0001 | 0/1 | 3109 | 119 | 8 | 25 | 73 | 5 | 7 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0002t0013 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0003t0002 | 0/0 | 3109 | 8 | 0 | 4 | 3 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0003t0003 | 0/0 | 3109 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0003t0004 | 0/0 | 3109 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0003t0005 | 0/0 | 3109 | 2 | 0 | 0 | 0 | 1 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0003t0007 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0004t0001 | 0/0 | 3109 | 11 | 0 | 1 | 9 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0001c0005t0001 | 0/0 | 3109 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0002c0006t0002 | 0/0 | 3109 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0003c0007t0004 | 0/0 | 3109 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0004c0010t0003 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0005c0011t0003 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0006c0014t0001 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0007c0013t0001 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0008c0012t0003 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0009c0015t0002 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0010c0008t0009 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
a0011c0009t0009 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | copy fasta | chr7 | 151336812 | 151383449 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0011g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0012g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0013g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0005g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0005t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0002c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0002c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0003c0007t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0003c0007t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0004c0010t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0005c0011t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0006c0014t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0007c0013t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0008c0012t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0009c0015t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0010c0008t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0011c0009t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0354 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0341 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0364 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00140 | hp2 | a0001 | c0003 | t0002 | g0308 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0348 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0107 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00323 | hp1 | a0001 | c0003 | t0005 | g0310 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00423 | hp2 | a0001 | c0003 | t0002 | g0242 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0323 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00621 | hp1 | a0001 | c0003 | t0004 | g0189 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0344 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0334 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0369 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01074 | hp1 | a0003 | c0007 | t0004 | g0314 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0352 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0358 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0340 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01106 | hp1 | a0001 | c0001 | t0012 | g0286 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0316 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0035 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0330 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0376 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01243 | hp2 | a0003 | c0007 | t0004 | g0304 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0257 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01256 | hp2 | a0001 | c0003 | t0002 | g0336 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0337 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0324 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0365 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0374 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0353 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01496 | hp2 | a0001 | c0004 | t0001 | g0174 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0327 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0277 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0342 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0278 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0319 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0265 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0355 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02027 | hp2 | a0009 | c0015 | t0002 | g0124 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02055 | hp2 | a0004 | c0010 | t0003 | g0208 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0335 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02080 | hp1 | a0001 | c0003 | t0002 | g0104 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0100 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | CDX | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CDX | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02257 | hp2 | a0005 | c0011 | t0003 | g0188 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0372 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0370 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0261 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0185 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0315 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0359 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0144 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0322 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0289 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0202 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0357 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02683 | hp2 | a0001 | c0002 | t0013 | g0285 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0373 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02698 | hp2 | a0008 | c0012 | t0003 | g0162 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0106 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0333 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0325 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0349 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0306 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0362 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0375 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0371 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0158 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0339 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03654 | hp1 | a0001 | c0003 | t0005 | g0366 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03654 | hp2 | a0001 | c0001 | t0011 | g0010 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0155 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0218 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0287 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0293 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03831 | hp1 | a0001 | c0004 | t0001 | g0360 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0356 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0332 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0347 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0111 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0329 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0117 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0331 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0305 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0112 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0368 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0234 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0307 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18906 | hp1 | a0001 | c0005 | t0001 | g0183 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0378 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18947 | hp1 | a0002 | c0006 | t0002 | g0092 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18951 | hp2 | a0006 | c0014 | t0001 | g0298 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18957 | hp2 | a0001 | c0003 | t0002 | g0120 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18964 | hp1 | a0001 | c0003 | t0004 | g0191 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18971 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18980 | hp2 | a0010 | c0008 | t0009 | g0004 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18988 | hp2 | a0007 | c0013 | t0001 | g0169 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18989 | hp1 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19003 | hp1 | a0011 | c0009 | t0009 | g0070 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19004 | hp2 | a0001 | c0004 | t0001 | g0080 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19011 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19012 | hp1 | a0001 | c0004 | t0001 | g0116 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19012 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0200 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19057 | hp2 | a0001 | c0004 | t0001 | g0055 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19064 | hp2 | a0002 | c0006 | t0002 | g0089 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0214 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19087 | hp2 | a0001 | c0004 | t0001 | g0203 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | ASW | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0266 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0363 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0309 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0279 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0351 | SAS | GIH | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | GIH | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0343 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0345 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02486 | hp2 | a0001 | c0003 | t0007 | g0259 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02559 | hp2 | a0001 | c0003 | t0003 | g0338 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03471 | hp1 | a0001 | c0005 | t0001 | g0275 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0346 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0377 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0301 | REF | REF | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0361 | REF | REF | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151345361
|
G | T | 1 | a0003 | 2 | HG01074.hp1 HG01243.hp2 |
missense_variant | MODERATE | c.12G>T | p.Lys4Asn | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/15 | 49/3109 | 12/1848 | 4/615 | chr7 | 151345361 | ||
chr7:151345387
|
A | G | 1 | a0002 | 2 | NA18947.hp1 NA19064.hp2 |
missense_variant | MODERATE | c.38A>G | p.Gln13Arg | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/15 | 75/3109 | 38/1848 | 13/615 | chr7 | 151345387 | ||
chr7:151349109
|
T | G | 2 | a0010a0011 | 2 | NA18980.hp2 NA19003.hp1 |
missense_variant | MODERATE | c.154T>G | p.Cys52Gly | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/15 | 191/3109 | 154/1848 | 52/615 | chr7 | 151349109 | ||
chr7:151355891
|
A | G | 1 | a0009 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.539A>G | p.Lys180Arg | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/15 | 576/3109 | 539/1848 | 180/615 | chr7 | 151355891 | ||
chr7:151360154
|
C | T | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.707C>T | p.Ala236Val | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 744/3109 | 707/1848 | 236/615 | chr7 | 151360154 | ||
chr7:151360158
|
G | A | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.711G>A | p.Met237Ile | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 748/3109 | 711/1848 | 237/615 | chr7 | 151360158 | ||
chr7:151360159
|
G | T | 1 | a0011 | 1 | NA19003.hp1 | stop_gained | HIGH | c.712G>T | p.Gly238* | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 749/3109 | 712/1848 | 238/615 | chr7 | 151360159 | ||
chr7:151360160
|
G | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.713G>C | p.Gly238Ala | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 750/3109 | 713/1848 | 238/615 | chr7 | 151360160 | ||
chr7:151360162
|
T | G | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.715T>G | p.Tyr239Asp | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 752/3109 | 715/1848 | 239/615 | chr7 | 151360162 | ||
chr7:151360178
|
G | T | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.731G>T | p.Arg244Ile | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 768/3109 | 731/1848 | 244/615 | chr7 | 151360178 | ||
chr7:151360184
|
T | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.737T>C | p.Phe246Ser | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 774/3109 | 737/1848 | 246/615 | chr7 | 151360184 | ||
chr7:151360189
|
A | T | 1 | a0011 | 1 | NA19003.hp1 | stop_gained | HIGH | c.742A>T | p.Lys248* | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 779/3109 | 742/1848 | 248/615 | chr7 | 151360189 | ||
chr7:151360191
|
A | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.744A>C | p.Lys248Asn | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 781/3109 | 744/1848 | 248/615 | chr7 | 151360191 | ||
chr7:151360195
|
A | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.748A>C | p.Lys250Gln | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 785/3109 | 748/1848 | 250/615 | chr7 | 151360195 | ||
chr7:151360200
|
A | T | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.753A>T | p.Glu251Asp | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 790/3109 | 753/1848 | 251/615 | chr7 | 151360200 | ||
chr7:151360201
|
T | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.754T>C | p.Tyr252His | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 791/3109 | 754/1848 | 252/615 | chr7 | 151360201 | ||
chr7:151367016
|
G | A | 1 | a0004 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.878G>A | p.Arg293His | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/15 | 915/3109 | 878/1848 | 293/615 | chr7 | 151367016 | ||
chr7:151367955
|
A | G | 1 | a0008 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1082A>G | p.Glu361Gly | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/15 | 1119/3109 | 1082/1848 | 361/615 | chr7 | 151367955 | ||
chr7:151374139
|
C | T | 1 | a0005 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1291C>T | p.Arg431Cys | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/15 | 1328/3109 | 1291/1848 | 431/615 | chr7 | 151374139 | ||
chr7:151375929
|
G | A | 1 | a0007 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.1477G>A | p.Glu493Lys | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/15 | 1514/3109 | 1477/1848 | 493/615 | chr7 | 151375929 | ||
chr7:151376748
|
G | A | 1 | a0006 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1606G>A | p.Glu536Lys | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 14/15 | 1643/3109 | 1606/1848 | 536/615 | chr7 | 151376748 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151355889
|
C | T | 1 | a0001c0005 | 2 | HG03471.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.537C>T | p.Ala179Ala | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/15 | 574/3109 | 537/1848 | 179/615 | chr7 | 151355889 | ||
chr7:151360164
|
T | C | 1 | a0011c0009 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.717T>C | p.Tyr239Tyr | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 754/3109 | 717/1848 | 239/615 | chr7 | 151360164 | ||
chr7:151366978
|
C | T | 6 | a0001c0002a0001c0003a0006c0014others(3): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
synonymous_variant | LOW | c.840C>T | p.Tyr280Tyr | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/15 | 877/3109 | 840/1848 | 280/615 | chr7 | 151366978 | ||
chr7:151377210
|
A | G | 6 | a0001c0002a0001c0004a0006c0014others(3): Show | 135 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(132): Show |
synonymous_variant | LOW | c.1833A>G | p.Ala611Ala | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 1870/3109 | 1833/1848 | 611/615 | chr7 | 151377210 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151377393
|
G | A | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(7): Show | 165 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*168G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 168 | chr7 | 151377393 | |||||
chr7:151377400
|
C | T | 2 | a0001c0001t0007a0001c0003t0007 | 7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*175C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 175 | chr7 | 151377400 | |||||
chr7:151377432
|
C | A | 1 | a0001c0002t0013 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 207 | chr7 | 151377432 | |||||
chr7:151377577
|
C | T | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(6): Show | 164 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 352 | chr7 | 151377577 | |||||
chr7:151377657
|
G | A | 1 | a0001c0001t0011 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 432 | chr7 | 151377657 | |||||
chr7:151377803
|
G | C | 5 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(2): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 578 | chr7 | 151377803 | |||||
chr7:151378071
|
T | C | 1 | a0001c0001t0006 | 10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*846T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 846 | chr7 | 151378071 | |||||
chr7:151378170
|
G | A | 2 | a0010c0008t0009a0011c0009t0009 | 2 | NA18980.hp2 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*945G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 945 | chr7 | 151378170 | |||||
chr7:151378222
|
A | G | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(20): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
3_prime_UTR_variant | MODIFIER | c.*997A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 997 | chr7 | 151378222 | |||||
chr7:151378237
|
T | C | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0012others(2): Show | 61 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1012T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 1012 | chr7 | 151378237 | |||||
chr7:151378308
|
G | T | 1 | a0001c0001t0012 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 1083 | chr7 | 151378308 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151341872
|
T | C | 274 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(271): Show | 297 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.-3+26T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341872 | ||||||
chr7:151341918
|
C | G | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG00323.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-3+72C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341918 | ||||||
chr7:151341931
|
C | G | 1 | a0001c0002t0001g0282 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-3+85C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341931 | ||||||
chr7:151341935
|
T | C | 130 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(127): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-3+89T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341935 | ||||||
chr7:151342017
|
G | A | 1 | a0001c0002t0013g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-3+171G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342017 | ||||||
chr7:151342058
|
T | G | 1 | a0001c0002t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3+212T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342058 | ||||||
chr7:151342093
|
T | C | 32 | a0001c0001t0002g0146a0001c0001t0002g0153a0001c0001t0002g0154others(29): Show | 32 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+247T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342093 | ||||||
chr7:151342187
|
C | G | 1 | a0001c0001t0002g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-3+341C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342187 | ||||||
chr7:151342349
|
A | G | 32 | a0001c0001t0002g0146a0001c0001t0002g0153a0001c0001t0002g0154others(29): Show | 32 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+503A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342349 | ||||||
chr7:151342470
|
G | A | 1 | a0001c0001t0004g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3+624G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342470 | ||||||
chr7:151342638
|
G | A | 1 | a0001c0001t0004g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3+792G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342638 | ||||||
chr7:151342720
|
C | T | 1 | a0001c0001t0007g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-3+874C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342720 | ||||||
chr7:151342757
|
G | A | 1 | a0001c0001t0012g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-3+911G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342757 | ||||||
chr7:151342828
|
A | T | 1 | a0001c0002t0001g0280 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-3+982A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342828 | ||||||
chr7:151342864
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+1018G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342864 | ||||||
chr7:151342970
|
G | A | 1 | a0001c0001t0004g0287 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-3+1124G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342970 | ||||||
chr7:151343021
|
T | C | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0007g0182others(2): Show | 5 | HG02615.hp2 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+1175T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343021 | ||||||
chr7:151343041
|
A | G | 1 | a0001c0002t0001g0378 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-3+1195A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343041 | ||||||
chr7:151343092
|
G | A | 5 | a0001c0001t0003g0017a0001c0001t0003g0187a0001c0001t0004g0184others(2): Show | 6 | HG02572.hp1 HG02965.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+1246G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343092 | ||||||
chr7:151343165
|
A | G | 8 | a0001c0001t0002g0274a0001c0001t0003g0273a0001c0001t0003g0276others(5): Show | 8 | HG01515.hp2 HG01517.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+1319A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343165 | ||||||
chr7:151343246
|
C | T | 2 | a0001c0001t0002g0271a0001c0001t0004g0270 | 2 | NA19002.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-3+1400C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343246 | ||||||
chr7:151343308
|
G | A | 318 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(315): Show | 350 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.-3+1462G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343308 | ||||||
chr7:151343348
|
A | G | 20 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0256others(17): Show | 25 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3+1502A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343348 | ||||||
chr7:151343518
|
G | A | 1 | a0001c0001t0002g0288 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3+1672G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343518 | ||||||
chr7:151343566
|
T | C | 32 | a0001c0001t0002g0146a0001c0001t0002g0153a0001c0001t0002g0154others(29): Show | 32 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+1720T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343566 | ||||||
chr7:151343567
|
C | T | 48 | a0001c0001t0002g0020a0001c0001t0002g0219a0001c0001t0002g0220others(45): Show | 50 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-3+1721C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343567 | ||||||
chr7:151343589
|
G | A | 1 | a0001c0001t0006g0289 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+1743G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343589 | ||||||
chr7:151343600
|
C | G | 49 | a0001c0001t0002g0020a0001c0001t0002g0219a0001c0001t0002g0220others(46): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-2-1748C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343600 | ||||||
chr7:151343853
|
T | A | 1 | a0001c0001t0003g0331 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-2-1495T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343853 | ||||||
chr7:151343879
|
A | G | 16 | a0001c0001t0003g0256a0001c0001t0003g0258a0001c0001t0003g0262others(13): Show | 21 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2-1469A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343879 | ||||||
chr7:151343985
|
T | C | 1 | a0005c0011t0003g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2-1363T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343985 | ||||||
chr7:151344033
|
C | T | 1 | a0001c0003t0002g0330 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2-1315C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344033 | ||||||
chr7:151344042
|
G | T | 1 | a0001c0003t0002g0330 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2-1306G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344042 | ||||||
chr7:151344070
|
A | G | 27 | a0001c0001t0002g0139a0001c0001t0003g0179a0001c0001t0003g0180others(24): Show | 32 | HG00735.hp1 HG01243.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2-1278A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344070 | ||||||
chr7:151344151
|
A | G | 13 | a0001c0001t0003g0258a0001c0001t0003g0262a0001c0001t0003g0264others(10): Show | 18 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-1197A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344151 | ||||||
chr7:151344167
|
T | C | 2 | a0001c0002t0001g0290a0001c0002t0001g0291 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-2-1181T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344167 | ||||||
chr7:151344176
|
C | G | 1 | a0001c0001t0004g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2-1172C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344176 | ||||||
chr7:151344180
|
C | CA | 34 | a0001c0001t0002g0195a0001c0001t0003g0179a0001c0001t0003g0205others(31): Show | 35 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.-2-1135dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
C | CAA | 22 | a0001c0001t0002g0018a0001c0001t0002g0190a0001c0001t0002g0192others(19): Show | 23 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-2-1136_-2-1135dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
C | CAAA | 8 | a0001c0001t0004g0335a0001c0002t0001g0292a0001c0002t0001g0334others(5): Show | 8 | HG00621.hp1 HG00642.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-1137_-2-1135dup others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0003g0156others(4): Show | 7 | HG01070.hp1 HG02148.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-1144_-2-1135dup others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0003g0332others(3): Show | 6 | HG00639.hp1 HG01192.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1145_-2-1135dup others(11): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0002t0001g0147others(1): Show | 4 | HG01346.hp2 HG02738.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-1146_-2-1135dup others(12): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-2-1149_-2-1135dup others(15): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0004g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2-1151_-2-1135dup others(17): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
CA | C | 6 | a0001c0001t0003g0180a0001c0001t0003g0211a0001c0001t0003g0376others(3): Show | 6 | HG01168.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-1135delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
CAAAAAA | C | 12 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0172others(9): Show | 12 | HG01069.hp2 HG01496.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-1140_-2-1135del others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0319others(12): Show | 18 | HG00597.hp2 HG01256.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-1145_-2-1135del others(11): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0002g0199a0001c0001t0003g0258a0001c0001t0004g0006others(2): Show | 8 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-1148_-2-1135del others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
CAAAAAAA others(8): Show |
C | 26 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0038others(23): Show | 29 | HG00735.hp1 HG01109.hp1 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-1149_-2-1135del others(15): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
CAAAAAAA others(9): Show |
C | 122 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(119): Show | 136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-2-1150_-2-1135del others(16): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344180
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138 | 3 | HG00609.hp2 HG01257.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-2-1151_-2-1135del others(17): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | |||||
chr7:151344210
|
A | G | 2 | a0001c0001t0002g0271a0001c0001t0007g0255 | 2 | HG02922.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-2-1138A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344210 | ||||||
chr7:151344211
|
A | AGTAG | 14 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0003g0273others(11): Show | 15 | HG00438.hp2 HG00673.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-1137_-2-1136ins others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344211 | ||||||
chr7:151344211
|
A | G | 39 | a0001c0001t0002g0020a0001c0001t0002g0244a0001c0001t0002g0248others(36): Show | 40 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2-1137A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344211 | ||||||
chr7:151344212
|
A | T | 39 | a0001c0001t0002g0020a0001c0001t0002g0244a0001c0001t0002g0248others(36): Show | 40 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2-1136A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344212 | ||||||
chr7:151344213
|
A | G | 2 | a0001c0001t0002g0271a0001c0001t0007g0255 | 2 | HG02922.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-2-1135A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344213 | ||||||
chr7:151344213
|
A | T | 16 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0003g0273others(13): Show | 17 | HG00438.hp2 HG00673.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2-1135A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344213 | ||||||
chr7:151344214
|
G | GATGT | 37 | a0001c0001t0002g0020a0001c0001t0002g0244a0001c0001t0002g0248others(34): Show | 38 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-2-1134_-2-1133ins others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344214 | ||||||
chr7:151344214
|
G | GT | 16 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0003g0273others(13): Show | 17 | HG00438.hp2 HG00673.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2-1133dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344214 | |||||
chr7:151344214
|
G | T | 2 | a0001c0001t0002g0271a0001c0001t0007g0255 | 2 | HG02922.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-2-1134G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344214 | ||||||
chr7:151344248
|
T | C | 1 | a0001c0002t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-2-1100T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344248 | ||||||
chr7:151344300
|
G | A | 1 | a0001c0001t0003g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2-1048G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344300 | ||||||
chr7:151344324
|
A | G | 1 | a0001c0001t0007g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-2-1024A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344324 | ||||||
chr7:151344333
|
C | T | 24 | a0001c0001t0003g0017a0001c0001t0003g0134a0001c0001t0003g0135others(21): Show | 30 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2-1015C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344333 | ||||||
chr7:151344334
|
G | A | 1 | a0001c0001t0002g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-2-1014G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344334 | ||||||
chr7:151344386
|
C | G | 3 | a0001c0001t0002g0288a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-962C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344386 | ||||||
chr7:151344425
|
C | T | 1 | a0001c0001t0007g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-2-923C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344425 | ||||||
chr7:151344435
|
C | T | 1 | a0001c0001t0003g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-2-913C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344435 | ||||||
chr7:151344467
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | NA18970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-2-881C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344467 | ||||||
chr7:151344580
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2-768G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344580 | ||||||
chr7:151344631
|
T | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0319 | 3 | HG01256.hp1 HG01261.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-2-717T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344631 | ||||||
chr7:151344632
|
C | G | 1 | a0001c0001t0008g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-716C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344632 | ||||||
chr7:151344683
|
G | A | 4 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | HG03490.hp1 HG03710.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-665G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344683 | ||||||
chr7:151344739
|
C | CGCCTGTA others(126): Show |
6 | a0001c0001t0002g0037a0001c0001t0002g0128a0001c0001t0002g0173others(3): Show | 6 | HG01496.hp2 HG01943.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-493_-2-492insTG others(131): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344739 | |||||
chr7:151344739
|
C | CGCCTGTA others(259): Show |
1 | a0001c0002t0001g0127 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-2-493_-2-492insTG others(264): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344739 | |||||
chr7:151344739
|
C | CGCCTGTA others(392): Show |
1 | a0001c0001t0002g0130 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-2-493_-2-492insTG others(397): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344739 | |||||
chr7:151344770
|
T | C | 5 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-578T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344770 | ||||||
chr7:151344776
|
G | A | 5 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-572G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344776 | ||||||
chr7:151344835
|
A | ACTAAAAA others(146): Show |
1 | a0001c0001t0004g0129 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-2-493_-2-492insTG others(151): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344835 | |||||
chr7:151344856
|
C | T | 109 | a0001c0001t0002g0015a0001c0001t0002g0020a0001c0001t0002g0038others(106): Show | 124 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(121): Show |
intron_variant | MODIFIER | c.-2-492C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344856 | ||||||
chr7:151344860
|
C | T | 7 | a0001c0001t0003g0331a0001c0001t0003g0355a0001c0001t0003g0369others(4): Show | 8 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-488C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344860 | ||||||
chr7:151344861
|
G | A | 1 | a0001c0002t0001g0193 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-2-487G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344861 | ||||||
chr7:151344866
|
G | A | 1 | a0001c0001t0008g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-482G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344866 | ||||||
chr7:151344868
|
C | T | 260 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(257): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-2-480C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344868 | ||||||
chr7:151344869
|
G | A | 7 | a0001c0001t0003g0315a0001c0001t0003g0320a0001c0001t0006g0008others(4): Show | 10 | HG02258.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-479G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344869 | ||||||
chr7:151344870
|
C | G | 1 | a0001c0002t0001g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-2-478C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344870 | ||||||
chr7:151344871
|
A | G | 2 | a0001c0002t0001g0060a0001c0002t0001g0143 | 2 | NA18971.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-2-477A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344871 | ||||||
chr7:151344872
|
T | C | 220 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(217): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-2-476T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344872 | ||||||
chr7:151344903
|
T | G | 5 | a0001c0001t0003g0026a0001c0001t0003g0262a0001c0001t0003g0264others(2): Show | 6 | HG00735.hp1 HG01256.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-445T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344903 | ||||||
chr7:151344916
|
C | G | 2 | a0001c0001t0003g0322a0001c0005t0001g0183 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-432C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344916 | ||||||
chr7:151344917
|
T | G | 7 | a0001c0001t0002g0199a0001c0001t0003g0258a0001c0001t0004g0021others(4): Show | 8 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-431T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344917 | ||||||
chr7:151344925
|
A | G | 8 | a0001c0001t0003g0040a0001c0001t0004g0354a0001c0002t0001g0148others(5): Show | 8 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-423A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344925 | ||||||
chr7:151344928
|
G | A | 9 | a0001c0001t0003g0040a0001c0001t0004g0354a0001c0001t0005g0325others(6): Show | 9 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-420G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344928 | ||||||
chr7:151344941
|
A | C | 1 | a0001c0002t0001g0016 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.-2-407A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344941 | ||||||
chr7:151344943
|
T | C | 8 | a0001c0001t0003g0264a0001c0001t0003g0315a0001c0001t0006g0008others(5): Show | 12 | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-405T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344943 | ||||||
chr7:151344948
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0303 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-2-400C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344948 | ||||||
chr7:151344979
|
G | A | 7 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0274others(4): Show | 10 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-369G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344979 | ||||||
chr7:151344987
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0281 | 2 | NA18948.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-2-361G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344987 | ||||||
chr7:151344995
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0002t0001g0377 | 3 | NA18994.hp1 NA18999.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-2-353G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344995 | ||||||
chr7:151345006
|
G | A | 1 | a0001c0004t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-2-342G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345006 | ||||||
chr7:151345027
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2-321C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345027 | ||||||
chr7:151345151
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-2-197G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345151 | ||||||
chr7:151345197
|
A | G | 78 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(75): Show | 85 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-2-151A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345197 | ||||||
chr7:151345691
|
C | T | 291 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(288): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.117+225C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151345691 | ||||||
chr7:151346087
|
T | A | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.117+621T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346087 | ||||||
chr7:151346135
|
T | C | 19 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(16): Show | 23 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+669T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346135 | ||||||
chr7:151346186
|
G | T | 46 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0017others(43): Show | 55 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.117+720G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346186 | ||||||
chr7:151346195
|
T | G | 1 | a0001c0001t0003g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+729T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346195 | ||||||
chr7:151346199
|
T | A | 1 | a0001c0001t0003g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+733T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346199 | ||||||
chr7:151346200
|
T | A | 1 | a0001c0001t0003g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+734T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346200 | ||||||
chr7:151346242
|
C | T | 1 | a0001c0001t0004g0354 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.117+776C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346242 | ||||||
chr7:151346427
|
G | C | 1 | a0001c0001t0002g0037 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.117+961G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346427 | ||||||
chr7:151346584
|
G | T | 48 | a0001c0001t0002g0038a0001c0001t0002g0139a0001c0001t0002g0199others(45): Show | 57 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.117+1118G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346584 | ||||||
chr7:151346614
|
G | A | 310 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(307): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.117+1148G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346614 | ||||||
chr7:151346643
|
G | T | 3 | a0001c0001t0002g0288a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.117+1177G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346643 | ||||||
chr7:151346661
|
C | T | 8 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(5): Show | 8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+1195C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346661 | ||||||
chr7:151346726
|
C | G | 1 | a0001c0004t0001g0203 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.117+1260C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346726 | ||||||
chr7:151346770
|
G | T | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0267others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+1304G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346770 | ||||||
chr7:151346901
|
G | A | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+1435G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346901 | ||||||
chr7:151346949
|
G | A | 316 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(313): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.117+1483G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346949 | ||||||
chr7:151347271
|
G | A | 1 | a0001c0001t0004g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.118-1802G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347271 | ||||||
chr7:151347326
|
C | T | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1747C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347326 | ||||||
chr7:151347418
|
G | GA | 316 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(313): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.118-1646dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151347418 | |||||
chr7:151347450
|
T | C | 1 | a0001c0001t0003g0350 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.118-1623T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347450 | ||||||
chr7:151347464
|
T | C | 1 | a0001c0001t0004g0129 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.118-1609T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347464 | ||||||
chr7:151347466
|
C | T | 1 | a0001c0001t0004g0129 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.118-1607C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347466 | ||||||
chr7:151347490
|
A | C | 22 | a0001c0001t0004g0007a0001c0001t0004g0023a0001c0001t0004g0031others(19): Show | 26 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.118-1583A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347490 | ||||||
chr7:151347503
|
G | T | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0267others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1570G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347503 | ||||||
chr7:151347505
|
T | C | 288 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(285): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.118-1568T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347505 | ||||||
chr7:151347571
|
C | T | 25 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0017others(22): Show | 30 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.118-1502C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347571 | ||||||
chr7:151347671
|
G | A | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1402G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347671 | ||||||
chr7:151347749
|
G | A | 5 | a0001c0001t0004g0031a0001c0001t0004g0155a0001c0001t0004g0218others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-1324G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347749 | ||||||
chr7:151347752
|
C | A | 19 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(16): Show | 23 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.118-1321C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347752 | ||||||
chr7:151347807
|
C | G | 3 | a0001c0002t0001g0062a0001c0002t0001g0103a0001c0003t0002g0104 | 3 | HG00408.hp1 HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.118-1266C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347807 | ||||||
chr7:151347847
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.118-1226G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347847 | ||||||
chr7:151347943
|
A | T | 19 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(16): Show | 23 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.118-1130A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347943 | ||||||
chr7:151347978
|
C | T | 1 | a0001c0002t0001g0312 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.118-1095C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347978 | ||||||
chr7:151348075
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0199 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.118-998A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348075 | ||||||
chr7:151348237
|
A | G | 2 | a0001c0002t0001g0327a0001c0003t0002g0308 | 2 | HG00140.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.118-836A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348237 | ||||||
chr7:151348353
|
A | T | 1 | a0001c0002t0001g0105 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.118-720A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348353 | ||||||
chr7:151348370
|
G | C | 1 | a0001c0001t0004g0270 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.118-703G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348370 | ||||||
chr7:151348479
|
T | C | 338 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(335): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.118-594T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348479 | ||||||
chr7:151348569
|
C | CT | 9 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0041others(6): Show | 9 | HG00438.hp2 HG00735.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-480dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
C | CTT | 23 | a0001c0001t0004g0066a0001c0001t0004g0158a0001c0001t0004g0287others(20): Show | 24 | HG00099.hp1 HG01517.hp1 HG03041.hp1 others(21): Show |
intron_variant | MODIFIER | c.118-481_118-480dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
C | CTTT | 121 | a0001c0001t0002g0001a0001c0001t0002g0195a0001c0001t0002g0198others(118): Show | 130 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.118-482_118-480dup others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
C | CTTTT | 39 | a0001c0001t0001g0367a0001c0001t0003g0316a0001c0001t0003g0332others(36): Show | 39 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.118-483_118-480dup others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
CTT | C | 9 | a0001c0001t0002g0167a0001c0001t0003g0315a0001c0001t0006g0008others(6): Show | 13 | HG01993.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-481_118-480del others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
CTTT | C | 7 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(4): Show | 7 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-482_118-480del others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
CTTTT | C | 13 | a0001c0001t0002g0057a0001c0001t0002g0090a0001c0001t0002g0091others(10): Show | 14 | HG00099.hp2 HG00597.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.118-483_118-480del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
CTTTTT | C | 87 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(84): Show | 104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.118-484_118-480del others(5): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
CTTTTTT | C | 25 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0328others(22): Show | 29 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.118-485_118-480del others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348569
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0003t0007g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118-489_118-480del others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | |||||
chr7:151348710
|
G | A | 3 | a0001c0001t0002g0288a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.118-363G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348710 | ||||||
chr7:151348818
|
G | A | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0267others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-255G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348818 | ||||||
chr7:151348903
|
C | G | 337 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(334): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.118-170C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348903 | ||||||
chr7:151348908
|
C | G | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0267others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-165C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348908 | ||||||
chr7:151348936
|
A | G | 315 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(312): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.118-137A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348936 | ||||||
chr7:151348961
|
G | A | 1 | a0001c0002t0001g0067 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.118-112G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348961 | ||||||
chr7:151349020
|
T | A | 1 | a0001c0001t0004g0129 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.118-53T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151349020 | ||||||
chr7:151349032
|
T | A | 1 | a0001c0001t0004g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.118-41T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151349032 | ||||||
chr7:151349534
|
C | G | 1 | a0001c0001t0004g0270 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.285+294C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349534 | ||||||
chr7:151349563
|
C | T | 175 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(172): Show | 192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.285+323C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349563 | ||||||
chr7:151349643
|
A | G | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+403A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349643 | ||||||
chr7:151349663
|
C | T | 1 | a0001c0002t0001g0324 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.285+423C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349663 | ||||||
chr7:151349746
|
A | G | 316 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(313): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.285+506A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349746 | ||||||
chr7:151349810
|
C | T | 97 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0003g0157others(94): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.285+570C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349810 | ||||||
chr7:151349915
|
C | G | 259 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(256): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.285+675C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349915 | ||||||
chr7:151350035
|
C | T | 2 | a0002c0006t0002g0089a0002c0006t0002g0092 | 2 | NA18947.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.285+795C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350035 | ||||||
chr7:151350056
|
G | A | 231 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(228): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.285+816G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350056 | ||||||
chr7:151350060
|
G | C | 3 | a0001c0001t0002g0288a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.285+820G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350060 | ||||||
chr7:151350281
|
T | C | 1 | a0001c0002t0001g0301 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.285+1041T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350281 | ||||||
chr7:151350291
|
C | A | 11 | a0001c0002t0001g0009a0001c0002t0001g0068a0001c0002t0001g0093others(8): Show | 12 | NA18947.hp2 NA18951.hp2 NA18956.hp2 others(9): Show |
intron_variant | MODIFIER | c.285+1051C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350291 | ||||||
chr7:151350412
|
T | G | 24 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0350others(21): Show | 25 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.286-1012T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350412 | ||||||
chr7:151350424
|
A | G | 341 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(338): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.286-1000A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350424 | ||||||
chr7:151350459
|
A | G | 25 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0273others(22): Show | 26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-965A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350459 | ||||||
chr7:151350519
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.286-905A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350519 | ||||||
chr7:151350558
|
C | T | 1 | a0001c0001t0002g0138 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.286-866C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350558 | ||||||
chr7:151350562
|
G | C | 2 | a0001c0001t0002g0012a0001c0001t0002g0079 | 3 | HG00438.hp1 NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.286-862G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350562 | ||||||
chr7:151350585
|
G | C | 182 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(179): Show | 199 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.286-839G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350585 | ||||||
chr7:151350692
|
C | T | 1 | a0001c0002t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.286-732C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350692 | ||||||
chr7:151350764
|
C | T | 1 | a0001c0002t0001g0060 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.286-660C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350764 | ||||||
chr7:151350861
|
A | G | 259 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(256): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.286-563A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350861 | ||||||
chr7:151350897
|
C | CCA | 7 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0044others(4): Show | 9 | HG00438.hp1 HG00621.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.286-527_286-526ins others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350897 | ||||||
chr7:151350898
|
G | C | 7 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0044others(4): Show | 9 | HG00438.hp1 HG00621.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.286-526G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350898 | ||||||
chr7:151350900
|
T | C | 1 | a0001c0005t0001g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.286-524T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350900 | ||||||
chr7:151350926
|
A | G | 257 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(254): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.286-498A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350926 | ||||||
chr7:151350941
|
G | A | 1 | a0001c0002t0001g0227 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.286-483G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350941 | ||||||
chr7:151351398
|
G | A | 271 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(268): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.286-26G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151351398 | ||||||
chr7:151351621
|
G | A | 1 | a0001c0001t0007g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.344+139G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351621 | ||||||
chr7:151351830
|
T | C | 6 | a0001c0001t0002g0038a0001c0001t0007g0106a0001c0001t0007g0131others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+348T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351830 | ||||||
chr7:151351863
|
A | G | 5 | a0001c0001t0004g0007a0001c0001t0004g0110a0001c0001t0004g0184others(2): Show | 7 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+381A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351863 | ||||||
chr7:151351873
|
G | A | 1 | a0001c0002t0001g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.344+391G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351873 | ||||||
chr7:151351916
|
A | AAC | 46 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0039others(43): Show | 48 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.344+453_344+454dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | AACAC | 33 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0033others(30): Show | 37 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.344+451_344+454dup others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | AACACAC | 36 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0274others(33): Show | 40 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.344+449_344+454dup others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | AACACACA others(1): Show |
53 | a0001c0001t0002g0248a0001c0001t0003g0017a0001c0001t0003g0187others(50): Show | 60 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.344+447_344+454dup others(8): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | AACACACA others(3): Show |
9 | a0001c0001t0002g0038a0001c0001t0003g0315a0001c0001t0005g0111others(6): Show | 13 | HG02258.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.344+445_344+454dup others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | AACACACA others(5): Show |
11 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(8): Show | 11 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+443_344+454dup others(12): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | AACACACA others(7): Show |
8 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(5): Show | 8 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+441_344+454dup others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | AACACACA others(9): Show |
1 | a0001c0001t0003g0201 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344+439_344+454dup others(16): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | |||||
chr7:151351916
|
A | ATCACACA others(1): Show |
96 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0003g0032others(93): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.344+434_344+435ins others(8): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | ||||||
chr7:151351916
|
A | ATCACACA others(3): Show |
77 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(74): Show | 89 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.344+434_344+435ins others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | ||||||
chr7:151351916
|
A | ATCACACA others(5): Show |
5 | a0001c0001t0002g0050a0001c0001t0002g0082a0001c0001t0002g0154others(2): Show | 5 | HG00323.hp2 HG00609.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+434_344+435ins others(12): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | ||||||
chr7:151351916
|
A | ATCACACA others(7): Show |
1 | a0001c0001t0002g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.344+434_344+435ins others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | ||||||
chr7:151351917
|
A | T | 1 | a0001c0003t0002g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.344+435A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351917 | ||||||
chr7:151351939
|
T | C | 307 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(304): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.344+457T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351939 | ||||||
chr7:151352145
|
C | T | 284 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(281): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.344+663C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352145 | ||||||
chr7:151352251
|
A | G | 339 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(336): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.345-561A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352251 | ||||||
chr7:151352293
|
G | A | 5 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0033others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-519G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352293 | ||||||
chr7:151352321
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0199 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.345-491A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352321 | ||||||
chr7:151352417
|
A | C | 184 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(181): Show | 201 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.345-395A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352417 | ||||||
chr7:151352443
|
A | T | 11 | a0001c0001t0004g0027a0001c0001t0004g0066a0001c0001t0004g0158others(8): Show | 12 | HG00099.hp1 HG02647.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-369A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352443 | ||||||
chr7:151352512
|
T | C | 7 | a0001c0001t0003g0315a0001c0001t0006g0008a0001c0001t0006g0022others(4): Show | 11 | HG02258.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-300T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352512 | ||||||
chr7:151352537
|
G | A | 11 | a0001c0001t0004g0027a0001c0001t0004g0066a0001c0001t0004g0158others(8): Show | 12 | HG00099.hp1 HG02647.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-275G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352537 | ||||||
chr7:151352620
|
T | A | 1 | a0001c0001t0002g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.345-192T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352620 | ||||||
chr7:151352621
|
T | G | 1 | a0001c0001t0007g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.345-191T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352621 | ||||||
chr7:151352630
|
A | C | 13 | a0001c0001t0002g0038a0001c0001t0003g0315a0001c0001t0006g0008others(10): Show | 17 | HG02258.hp2 HG02572.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-182A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352630 | ||||||
chr7:151352653
|
G | T | 1 | a0001c0001t0003g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.345-159G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352653 | ||||||
chr7:151352720
|
G | A | 2 | a0001c0003t0002g0035a0001c0003t0003g0339 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.345-92G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352720 | ||||||
chr7:151352732
|
C | G | 12 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(9): Show | 12 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-80C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352732 | ||||||
chr7:151352732
|
C | T | 259 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(256): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.345-80C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352732 | ||||||
chr7:151352736
|
C | T | 2 | a0001c0001t0003g0313a0001c0001t0003g0357 | 2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.345-76C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352736 | ||||||
chr7:151352897
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(9): Show | 12 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+15G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151352897 | ||||||
chr7:151352942
|
C | A | 1 | a0001c0001t0003g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.415+60C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151352942 | ||||||
chr7:151353012
|
G | A | 1 | a0001c0001t0005g0365 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.415+130G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353012 | ||||||
chr7:151353072
|
T | C | 284 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(281): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.415+190T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353072 | ||||||
chr7:151353147
|
A | C | 23 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0273others(20): Show | 24 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+265A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353147 | ||||||
chr7:151353187
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.415+305A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353187 | ||||||
chr7:151353197
|
G | C | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+315G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353197 | ||||||
chr7:151353318
|
A | G | 339 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(336): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.415+436A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353318 | ||||||
chr7:151353528
|
C | T | 74 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(71): Show | 86 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.415+646C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353528 | ||||||
chr7:151353535
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0199 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.415+653A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353535 | ||||||
chr7:151353633
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.415+751C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353633 | ||||||
chr7:151353666
|
A | G | 6 | a0001c0001t0002g0038a0001c0001t0007g0106a0001c0001t0007g0131others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+784A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353666 | ||||||
chr7:151353722
|
C | A | 38 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0274others(35): Show | 42 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+840C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353722 | ||||||
chr7:151353733
|
T | C | 1 | a0001c0001t0007g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.415+851T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353733 | ||||||
chr7:151353734
|
G | A | 1 | a0001c0001t0003g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.415+852G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353734 | ||||||
chr7:151353750
|
G | A | 1 | a0001c0001t0003g0347 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.415+868G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353750 | ||||||
chr7:151354215
|
G | T | 1 | a0001c0001t0005g0056 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.415+1333G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354215 | ||||||
chr7:151354322
|
C | CT | 12 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(9): Show | 12 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-1431dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 151354322 | |||||
chr7:151354322
|
CT | C | 6 | a0001c0001t0002g0018a0001c0001t0002g0173a0001c0001t0003g0277others(3): Show | 7 | HG01515.hp2 HG01943.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-1431delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 151354322 | |||||
chr7:151354397
|
G | A | 5 | a0001c0001t0004g0007a0001c0001t0004g0110a0001c0001t0004g0184others(2): Show | 7 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-1371G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354397 | ||||||
chr7:151354418
|
A | T | 1 | a0001c0002t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.416-1350A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354418 | ||||||
chr7:151354437
|
G | A | 1 | a0001c0001t0004g0362 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.416-1331G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354437 | ||||||
chr7:151354524
|
T | C | 14 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0001t0004g0048others(11): Show | 15 | HG00423.hp1 HG02015.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.416-1244T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354524 | ||||||
chr7:151354715
|
A | T | 1 | a0001c0001t0005g0056 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.416-1053A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354715 | ||||||
chr7:151354719
|
C | T | 8 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(5): Show | 8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.416-1049C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354719 | ||||||
chr7:151355043
|
TG | T | 23 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0273others(20): Show | 24 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-723delG | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 151355043 | |||||
chr7:151355061
|
G | A | 277 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(274): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.416-707G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355061 | ||||||
chr7:151355211
|
C | T | 284 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(281): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.416-557C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355211 | ||||||
chr7:151355261
|
T | A | 1 | a0001c0001t0007g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.416-507T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355261 | ||||||
chr7:151355281
|
G | A | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.416-487G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355281 | ||||||
chr7:151355613
|
T | C | 284 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(281): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.416-155T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355613 | ||||||
chr7:151355633
|
A | C | 7 | a0001c0001t0003g0315a0001c0001t0006g0008a0001c0001t0006g0022others(4): Show | 11 | HG02258.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-135A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355633 | ||||||
chr7:151355760
|
T | A | 3 | a0001c0002t0001g0234a0001c0002t0001g0240a0001c0002t0001g0342 | 3 | HG01123.hp1 HG01517.hp1 HG04228.hp1 |
splice_region_variant&intron_variant | LOW | c.416-8T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355760 | ||||||
chr7:151355957
|
A | G | 272 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(269): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
splice_region_variant&intron_variant | LOW | c.598+7A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151355957 | ||||||
chr7:151356002
|
G | A | 1 | a0001c0001t0004g0326 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.598+52G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151356002 | ||||||
chr7:151356075
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0145 | 2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.599-53C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151356075 | ||||||
chr7:151356118
|
T | C | 8 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(5): Show | 8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-10T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151356118 | ||||||
chr7:151356358
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.693+136T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356358 | ||||||
chr7:151356458
|
T | G | 8 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(5): Show | 8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+236T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356458 | ||||||
chr7:151356474
|
A | C | 1 | a0007c0013t0001g0169 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.693+252A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356474 | ||||||
chr7:151356547
|
C | A | 38 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0274others(35): Show | 42 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.693+325C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356547 | ||||||
chr7:151356721
|
G | T | 5 | a0001c0001t0004g0007a0001c0001t0004g0110a0001c0001t0004g0184others(2): Show | 7 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+499G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356721 | ||||||
chr7:151356721
|
GT | G | 283 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(280): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.693+506delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151356721 | |||||
chr7:151356925
|
C | T | 2 | a0001c0002t0001g0232a0001c0002t0001g0299 | 2 | NA18947.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.693+703C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356925 | ||||||
chr7:151356944
|
C | T | 1 | a0001c0001t0003g0348 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.693+722C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356944 | ||||||
chr7:151356978
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.693+756A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356978 | ||||||
chr7:151357006
|
C | T | 2 | a0001c0003t0002g0336a0001c0003t0002g0337 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.693+784C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357006 | ||||||
chr7:151357083
|
C | T | 21 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0273others(18): Show | 22 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.693+861C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357083 | ||||||
chr7:151357087
|
G | A | 1 | a0001c0001t0004g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.693+865G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357087 | ||||||
chr7:151357127
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.693+905C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357127 | ||||||
chr7:151357128
|
C | T | 2 | a0001c0002t0001g0141a0001c0002t0001g0142 | 2 | NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.693+906C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357128 | ||||||
chr7:151357183
|
ATTT | A | 268 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(265): Show | 295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.693+979_693+981del others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357183 | |||||
chr7:151357183
|
ATTTT | A | 8 | a0001c0001t0002g0190a0001c0001t0002g0318a0001c0001t0004g0287others(5): Show | 8 | HG01192.hp2 HG02895.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+978_693+981del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357183 | |||||
chr7:151357270
|
C | T | 6 | a0001c0001t0002g0038a0001c0001t0007g0106a0001c0001t0007g0131others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+1048C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357270 | ||||||
chr7:151357502
|
T | C | 3 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0328 | 3 | HG02280.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.693+1280T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357502 | ||||||
chr7:151357506
|
G | A | 1 | a0001c0002t0001g0221 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.693+1284G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357506 | ||||||
chr7:151357608
|
G | GT | 7 | a0001c0001t0002g0079a0001c0001t0002g0081a0001c0001t0002g0095others(4): Show | 7 | HG00438.hp1 HG02080.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+1402dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357608 | |||||
chr7:151357608
|
GT | G | 115 | a0001c0001t0002g0038a0001c0001t0002g0042a0001c0001t0002g0146others(112): Show | 130 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.693+1402delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357608 | |||||
chr7:151357672
|
C | T | 76 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(73): Show | 88 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.693+1450C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357672 | ||||||
chr7:151357910
|
G | A | 22 | a0001c0001t0004g0007a0001c0001t0004g0023a0001c0001t0004g0031others(19): Show | 26 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.693+1688G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357910 | ||||||
chr7:151358013
|
G | A | 182 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(179): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.693+1791G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358013 | ||||||
chr7:151358164
|
G | A | 3 | a0001c0001t0002g0288a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.693+1942G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358164 | ||||||
chr7:151358329
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0136 | 2 | HG01257.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.694-1812C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358329 | ||||||
chr7:151358391
|
G | T | 1 | a0004c0010t0003g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.694-1750G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358391 | ||||||
chr7:151358443
|
AG | A | 6 | a0001c0001t0006g0008a0001c0001t0006g0022a0001c0001t0006g0025others(3): Show | 10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.694-1696delG | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151358443 | |||||
chr7:151358461
|
G | A | 2 | a0001c0001t0003g0017a0001c0001t0003g0187 | 3 | HG02970.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.694-1680G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358461 | ||||||
chr7:151358472
|
A | G | 322 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(319): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.694-1669A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358472 | ||||||
chr7:151358860
|
C | T | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.694-1281C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358860 | ||||||
chr7:151358926
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.694-1215G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358926 | ||||||
chr7:151359105
|
A | G | 25 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0273others(22): Show | 26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-1036A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359105 | ||||||
chr7:151359132
|
CTAGATGA others(6): Show |
C | 1 | a0011c0009t0009g0070 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-1008_694-996de others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359132 | ||||||
chr7:151359136
|
A | G | 4 | a0001c0001t0004g0011a0001c0001t0004g0048a0001c0001t0004g0098others(1): Show | 5 | HG02132.hp2 NA18941.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-1005A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359136 | ||||||
chr7:151359161
|
G | A | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.694-980G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359161 | ||||||
chr7:151359166
|
C | T | 1 | a0011c0009t0009g0070 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-975C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359166 | ||||||
chr7:151359265
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.694-876T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359265 | ||||||
chr7:151359282
|
C | CA | 45 | a0001c0001t0003g0017a0001c0001t0003g0033a0001c0001t0003g0179others(42): Show | 53 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.694-848dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359282 | |||||
chr7:151359282
|
C | CAA | 8 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0004g0023others(5): Show | 9 | HG01074.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.694-849_694-848dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359282 | |||||
chr7:151359367
|
T | C | 78 | a0001c0001t0002g0042a0001c0001t0002g0139a0001c0001t0002g0146others(75): Show | 91 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.694-774T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359367 | ||||||
chr7:151359384
|
A | G | 6 | a0001c0001t0006g0008a0001c0001t0006g0022a0001c0001t0006g0025others(3): Show | 10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.694-757A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359384 | ||||||
chr7:151359442
|
C | CA | 53 | a0001c0001t0003g0017a0001c0001t0003g0033a0001c0001t0003g0179others(50): Show | 62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.694-686dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359442 | |||||
chr7:151359507
|
C | CGTGGCTC others(36): Show |
5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-632_694-590dup others(43): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359507 | |||||
chr7:151359516
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.694-625C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359516 | ||||||
chr7:151359517
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.694-624G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359517 | ||||||
chr7:151359527
|
C | T | 5 | a0001c0001t0003g0331a0001c0001t0003g0352a0001c0001t0003g0355others(2): Show | 5 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-614C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359527 | ||||||
chr7:151359670
|
G | A | 25 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0273others(22): Show | 26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-471G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359670 | ||||||
chr7:151359725
|
C | T | 27 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0267others(24): Show | 31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.694-416C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359725 | ||||||
chr7:151359772
|
G | A | 51 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0017others(48): Show | 60 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.694-369G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359772 | ||||||
chr7:151359776
|
C | CA | 21 | a0001c0001t0003g0017a0001c0001t0003g0187a0001c0001t0003g0209others(18): Show | 26 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-358dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359776 | |||||
chr7:151359911
|
C | T | 76 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(73): Show | 88 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.694-230C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359911 | ||||||
chr7:151360061
|
T | C | 25 | a0001c0001t0002g0248a0001c0001t0003g0205a0001c0001t0003g0273others(22): Show | 26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-80T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360061 | ||||||
chr7:151360096
|
A | G | 2 | a0001c0001t0003g0201a0001c0001t0003g0315 | 2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.694-45A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360096 | ||||||
chr7:151360129
|
A | G | 1 | a0011c0009t0009g0070 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-12A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360129 | ||||||
chr7:151360130
|
T | A | 1 | a0011c0009t0009g0070 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-11T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360130 | ||||||
chr7:151360136
|
C | T | 1 | a0011c0009t0009g0070 | 1 | NA19003.hp1 | splice_region_variant&intron_variant | LOW | c.694-5C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360136 | ||||||
chr7:151360310
|
AC | A | 94 | a0001c0002t0001g0004a0001c0002t0001g0016a0001c0002t0001g0024others(91): Show | 99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.800+66delC | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360310 | |||||
chr7:151360386
|
T | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0199 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.800+139T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360386 | ||||||
chr7:151360468
|
C | T | 2 | a0001c0002t0001g0094a0001c0002t0001g0196 | 2 | NA18961.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.800+221C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360468 | ||||||
chr7:151360492
|
T | C | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.800+245T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360492 | ||||||
chr7:151360502
|
C | T | 1 | a0001c0001t0004g0346 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.800+255C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360502 | ||||||
chr7:151360532
|
G | T | 1 | a0001c0003t0003g0339 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.800+285G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360532 | ||||||
chr7:151360557
|
A | T | 8 | a0001c0001t0003g0201a0001c0001t0003g0315a0001c0001t0006g0008others(5): Show | 12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.800+310A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360557 | ||||||
chr7:151360599
|
A | G | 80 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(77): Show | 92 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.800+352A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360599 | ||||||
chr7:151360616
|
C | A | 2 | a0001c0002t0001g0168a0007c0013t0001g0169 | 2 | NA18954.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.800+369C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360616 | ||||||
chr7:151360628
|
A | AT | 53 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0017others(50): Show | 62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.800+389dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360628 | |||||
chr7:151360756
|
TCACAGGT others(9): Show |
T | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+528_800+543del others(16): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360756 | |||||
chr7:151360848
|
A | G | 318 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(315): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.800+601A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360848 | ||||||
chr7:151360895
|
TCAAAGTG others(137): Show |
T | 252 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(249): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.800+660_800+803del | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360895 | |||||
chr7:151360907
|
T | G | 1 | a0001c0001t0004g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.800+660T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360907 | ||||||
chr7:151360907
|
TATTACAG others(137): Show |
T | 1 | a0001c0002t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.800+675_800+818del | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360907 | |||||
chr7:151360934
|
C | CT | 8 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0267others(5): Show | 8 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.800+710dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360934 | |||||
chr7:151360934
|
CT | C | 18 | a0001c0001t0002g0166a0001c0001t0003g0201a0001c0001t0003g0278others(15): Show | 24 | HG01069.hp2 HG01074.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.800+710delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360934 | |||||
chr7:151360975
|
C | T | 9 | a0001c0001t0002g0038a0001c0001t0003g0201a0001c0001t0003g0315others(6): Show | 13 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.800+728C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360975 | ||||||
chr7:151361070
|
C | T | 6 | a0001c0001t0003g0347a0001c0001t0007g0106a0001c0001t0007g0131others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.800+823C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361070 | ||||||
chr7:151361153
|
C | A | 1 | a0001c0003t0005g0366 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.800+906C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361153 | ||||||
chr7:151361159
|
G | A | 1 | a0001c0001t0005g0371 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.800+912G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361159 | ||||||
chr7:151361537
|
A | T | 255 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(252): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.800+1290A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361537 | ||||||
chr7:151361563
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.800+1316G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361563 | ||||||
chr7:151361645
|
A | C | 3 | a0001c0001t0002g0288a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.800+1398A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361645 | ||||||
chr7:151361688
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.800+1441T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361688 | ||||||
chr7:151361739
|
T | C | 1 | a0005c0011t0003g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.800+1492T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361739 | ||||||
chr7:151361770
|
C | T | 1 | a0001c0002t0001g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.800+1523C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361770 | ||||||
chr7:151361838
|
A | G | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+1591A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361838 | ||||||
chr7:151362040
|
C | T | 1 | a0001c0003t0002g0330 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.800+1793C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362040 | ||||||
chr7:151362131
|
T | C | 313 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(310): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.800+1884T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362131 | ||||||
chr7:151362311
|
G | T | 2 | a0001c0001t0003g0201a0001c0001t0003g0315 | 2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.800+2064G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362311 | ||||||
chr7:151362353
|
T | C | 1 | a0001c0001t0004g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.800+2106T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362353 | ||||||
chr7:151362404
|
C | A | 1 | a0001c0002t0001g0327 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.800+2157C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362404 | ||||||
chr7:151362446
|
T | C | 52 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0274others(49): Show | 57 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.800+2199T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362446 | ||||||
chr7:151362451
|
G | C | 1 | a0001c0001t0002g0002 | 3 | HG01081.hp1 HG01109.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.800+2204G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362451 | ||||||
chr7:151362517
|
T | C | 8 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(5): Show | 8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.800+2270T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362517 | ||||||
chr7:151362575
|
A | T | 1 | a0001c0001t0003g0028 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.800+2328A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362575 | ||||||
chr7:151362648
|
G | T | 75 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(72): Show | 87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.800+2401G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362648 | ||||||
chr7:151362707
|
A | C | 53 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0017others(50): Show | 62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.800+2460A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362707 | ||||||
chr7:151362803
|
A | G | 31 | a0001c0002t0001g0009a0001c0002t0001g0047a0001c0002t0001g0068others(28): Show | 32 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.800+2556A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362803 | ||||||
chr7:151362855
|
C | T | 50 | a0001c0001t0003g0017a0001c0001t0003g0033a0001c0001t0003g0179others(47): Show | 59 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.800+2608C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362855 | ||||||
chr7:151362988
|
C | T | 255 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(252): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.800+2741C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362988 | ||||||
chr7:151363182
|
T | C | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+2935T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363182 | ||||||
chr7:151363417
|
G | A | 8 | a0001c0001t0003g0201a0001c0001t0003g0315a0001c0001t0006g0008others(5): Show | 12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.800+3170G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363417 | ||||||
chr7:151363453
|
T | TA | 59 | a0001c0001t0002g0038a0001c0001t0002g0042a0001c0001t0002g0139others(56): Show | 68 | HG00423.hp1 HG01069.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.800+3221dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363453 | |||||
chr7:151363453
|
T | TAAAA | 8 | a0001c0001t0003g0201a0001c0001t0003g0315a0001c0001t0006g0008others(5): Show | 12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.800+3218_800+3221d others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363453 | |||||
chr7:151363453
|
TA | T | 94 | a0001c0001t0002g0271a0001c0002t0001g0004a0001c0002t0001g0016others(91): Show | 99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.800+3221delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363453 | |||||
chr7:151363634
|
A | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0199 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.801-3305A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363634 | ||||||
chr7:151363721
|
T | C | 1 | a0001c0002t0001g0305 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.801-3218T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363721 | ||||||
chr7:151363751
|
GAA | G | 8 | a0001c0001t0003g0201a0001c0001t0003g0315a0001c0001t0006g0008others(5): Show | 12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.801-3183_801-3182d others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363751 | |||||
chr7:151363756
|
AAGTT | A | 53 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0001t0003g0017others(50): Show | 62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.801-3180_801-3177d others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363756 | |||||
chr7:151363954
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.801-2985C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363954 | ||||||
chr7:151364019
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0199 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.801-2920C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364019 | ||||||
chr7:151364051
|
C | A | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-2888C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364051 | ||||||
chr7:151364081
|
A | C | 3 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0328 | 3 | HG02280.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.801-2858A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364081 | ||||||
chr7:151364084
|
G | A | 9 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(6): Show | 9 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.801-2855G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364084 | ||||||
chr7:151364144
|
C | T | 1 | a0001c0002t0001g0016 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.801-2795C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364144 | ||||||
chr7:151364290
|
A | G | 314 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(311): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.801-2649A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364290 | ||||||
chr7:151364349
|
A | AG | 8 | a0001c0001t0003g0201a0001c0001t0003g0315a0001c0001t0006g0008others(5): Show | 12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.801-2588dupG | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364349 | |||||
chr7:151364397
|
G | C | 5 | a0001c0001t0004g0036a0001c0001t0004g0345a0001c0001t0004g0346others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.801-2542G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364397 | ||||||
chr7:151364432
|
CA | C | 220 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0042others(217): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.801-2498delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364432 | |||||
chr7:151364440
|
A | AC | 4 | a0001c0001t0002g0014a0001c0001t0002g0057a0001c0001t0002g0130others(1): Show | 5 | NA18940.hp2 NA18946.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-2499_801-2498i others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364440 | ||||||
chr7:151364441
|
A | C | 92 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(89): Show | 107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.801-2498A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364441 | ||||||
chr7:151364442
|
C | A | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(87): Show | 102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.801-2497C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364442 | ||||||
chr7:151364452
|
A | C | 4 | a0001c0001t0002g0038a0001c0001t0003g0179a0001c0001t0003g0180others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-2487A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364452 | ||||||
chr7:151364453
|
A | C | 306 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(303): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.801-2486A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364453 | ||||||
chr7:151364465
|
T | G | 3 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0328 | 3 | HG02280.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.801-2474T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364465 | ||||||
chr7:151364481
|
A | C | 314 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(311): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.801-2458A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364481 | ||||||
chr7:151364556
|
G | C | 1 | a0001c0001t0004g0326 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.801-2383G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364556 | ||||||
chr7:151364867
|
T | C | 317 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(314): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.801-2072T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364867 | ||||||
chr7:151364872
|
C | T | 1 | a0001c0002t0001g0282 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.801-2067C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364872 | ||||||
chr7:151364908
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.801-2031G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364908 | ||||||
chr7:151364974
|
A | AAATTTTT others(317): Show |
1 | a0001c0001t0004g0326 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.801-1952_801-1951i others(326): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364974 | |||||
chr7:151364984
|
T | A | 1 | a0011c0009t0009g0070 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.801-1955T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364984 | ||||||
chr7:151364992
|
AT | A | 9 | a0001c0001t0003g0201a0001c0001t0003g0315a0001c0001t0003g0357others(6): Show | 13 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.801-1935delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364992 | |||||
chr7:151365030
|
T | C | 322 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(319): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.801-1909T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365030 | ||||||
chr7:151365076
|
G | A | 2 | a0001c0001t0003g0340a0001c0001t0005g0365 | 2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.801-1863G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365076 | ||||||
chr7:151365078
|
C | A | 21 | a0001c0001t0003g0017a0001c0001t0003g0187a0001c0001t0003g0209others(18): Show | 26 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.801-1861C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365078 | ||||||
chr7:151365093
|
A | G | 317 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(314): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.801-1846A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365093 | ||||||
chr7:151365210
|
T | G | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1729T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365210 | ||||||
chr7:151365262
|
G | A | 96 | a0001c0002t0001g0004a0001c0002t0001g0016a0001c0002t0001g0024others(93): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.801-1677G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365262 | ||||||
chr7:151365318
|
CT | C | 299 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(296): Show | 330 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.801-1607delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151365318 | |||||
chr7:151365434
|
G | A | 7 | a0001c0002t0001g0009a0001c0002t0001g0068a0001c0002t0001g0093others(4): Show | 8 | NA18956.hp2 NA18970.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.801-1505G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365434 | ||||||
chr7:151365551
|
T | C | 1 | a0001c0001t0002g0095 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.801-1388T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365551 | ||||||
chr7:151365669
|
C | T | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1270C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365669 | ||||||
chr7:151365707
|
G | A | 1 | a0001c0003t0002g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.801-1232G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365707 | ||||||
chr7:151365714
|
A | G | 5 | a0001c0002t0001g0151a0001c0002t0001g0300a0001c0002t0001g0309others(2): Show | 5 | HG00738.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.801-1225A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365714 | ||||||
chr7:151365745
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.801-1194G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365745 | ||||||
chr7:151365766
|
G | A | 1 | a0001c0002t0001g0030 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.801-1173G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365766 | ||||||
chr7:151365890
|
C | CT | 253 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(250): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.801-1039dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151365890 | |||||
chr7:151365890
|
CT | C | 24 | a0001c0001t0002g0288a0001c0001t0002g0317a0001c0001t0002g0318others(21): Show | 29 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.801-1039delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151365890 | |||||
chr7:151365905
|
C | A | 4 | a0001c0001t0004g0011a0001c0001t0004g0048a0001c0001t0004g0098others(1): Show | 5 | HG02132.hp2 NA18941.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1034C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365905 | ||||||
chr7:151365910
|
A | G | 1 | a0001c0001t0003g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.801-1029A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365910 | ||||||
chr7:151366245
|
A | T | 1 | a0001c0001t0004g0027 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.801-694A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366245 | ||||||
chr7:151366404
|
G | C | 1 | a0001c0001t0004g0031 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.801-535G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366404 | ||||||
chr7:151366471
|
C | A | 2 | a0001c0001t0003g0179a0001c0001t0003g0180 | 2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.801-468C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366471 | ||||||
chr7:151366478
|
A | G | 5 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-461A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366478 | ||||||
chr7:151366519
|
T | TAAAG | 3 | a0001c0001t0002g0038a0001c0001t0003g0157a0001c0001t0003g0332 | 3 | HG02965.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.801-397_801-394dup others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151366519 | |||||
chr7:151366519
|
TAAAG | T | 327 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(324): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.801-397_801-394del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151366519 | |||||
chr7:151366547
|
G | A | 8 | a0001c0001t0002g0042a0001c0001t0002g0146a0001c0001t0002g0153others(5): Show | 8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.801-392G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366547 | ||||||
chr7:151366708
|
C | A | 6 | a0001c0001t0004g0023a0001c0001t0004g0257a0001c0001t0004g0265others(3): Show | 7 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.801-231C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366708 | ||||||
chr7:151366783
|
C | G | 1 | a0001c0003t0003g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.801-156C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366783 | ||||||
chr7:151367188
|
T | A | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.987+63T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367188 | ||||||
chr7:151367219
|
A | G | 336 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(333): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.987+94A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367219 | ||||||
chr7:151367336
|
A | G | 149 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0053others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.987+211A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367336 | ||||||
chr7:151367645
|
A | T | 1 | a0001c0002t0001g0122 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.988-216A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367645 | ||||||
chr7:151367646
|
C | T | 16 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0328others(13): Show | 19 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.988-215C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367646 | ||||||
chr7:151367672
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0004t0001g0174 | 3 | HG01496.hp2 HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.988-189A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367672 | ||||||
chr7:151367786
|
A | G | 120 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(117): Show | 139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.988-75A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367786 | ||||||
chr7:151368127
|
G | C | 4 | a0001c0001t0004g0027a0001c0001t0004g0326a0001c0001t0008g0200others(1): Show | 5 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+159G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/14 | chr7 | 151368127 | ||||||
chr7:151368388
|
C | T | 1 | a0001c0002t0001g0193 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1096-347C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/14 | chr7 | 151368388 | ||||||
chr7:151368590
|
A | G | 1 | a0001c0002t0001g0016 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1096-145A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/14 | chr7 | 151368590 | ||||||
chr7:151368992
|
GA | G | 6 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+107delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151368992 | |||||
chr7:151369071
|
G | A | 2 | a0001c0001t0003g0209a0004c0010t0003g0208 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1248+184G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369071 | ||||||
chr7:151369455
|
T | C | 135 | a0001c0001t0003g0032a0001c0001t0003g0135a0001c0001t0003g0258others(132): Show | 141 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1248+568T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369455 | ||||||
chr7:151369649
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1248+762A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369649 | ||||||
chr7:151369790
|
A | G | 1 | a0001c0001t0007g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1248+903A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369790 | ||||||
chr7:151370028
|
C | T | 8 | a0001c0001t0003g0201a0001c0001t0003g0315a0001c0001t0006g0008others(5): Show | 12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1248+1141C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370028 | ||||||
chr7:151370084
|
G | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0136 | 2 | HG01257.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1248+1197G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370084 | ||||||
chr7:151370097
|
CT | C | 15 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0042others(12): Show | 18 | HG01069.hp2 HG01070.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1248+1224delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151370097 | |||||
chr7:151370165
|
C | G | 2 | a0001c0001t0008g0200a0001c0001t0008g0202 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1248+1278C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370165 | ||||||
chr7:151370392
|
A | C | 1 | a0001c0001t0007g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1248+1505A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370392 | ||||||
chr7:151370503
|
A | T | 261 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(258): Show | 284 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1248+1616A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370503 | ||||||
chr7:151370692
|
C | G | 112 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(109): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1248+1805C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370692 | ||||||
chr7:151371146
|
C | T | 2 | a0001c0001t0003g0043a0001c0001t0003g0156 | 2 | HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1248+2259C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371146 | ||||||
chr7:151371176
|
C | T | 329 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(326): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1248+2289C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371176 | ||||||
chr7:151371180
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1248+2293G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371180 | ||||||
chr7:151371180
|
G | C | 3 | a0001c0003t0002g0308a0001c0003t0002g0336a0001c0003t0002g0337 | 3 | HG00140.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1248+2293G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371180 | ||||||
chr7:151371363
|
A | AC | 249 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(246): Show | 272 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1248+2482dupC | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151371363 | |||||
chr7:151371363
|
A | ACC | 16 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0087others(13): Show | 16 | HG01934.hp1 HG02135.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.1248+2481_1248+248 others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151371363 | |||||
chr7:151371554
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1249-2543G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371554 | ||||||
chr7:151371647
|
C | T | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1249-2450C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371647 | ||||||
chr7:151371672
|
A | T | 1 | a0001c0001t0002g0095 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1249-2425A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371672 | ||||||
chr7:151371836
|
C | T | 8 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(5): Show | 8 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-2261C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371836 | ||||||
chr7:151371843
|
C | T | 1 | a0001c0002t0001g0341 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1249-2254C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371843 | ||||||
chr7:151372043
|
T | A | 2 | a0001c0002t0001g0300a0001c0002t0001g0309 | 2 | HG02559.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1249-2054T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372043 | ||||||
chr7:151372138
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1249-1959C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372138 | ||||||
chr7:151372170
|
A | G | 2 | a0001c0001t0008g0200a0001c0001t0008g0202 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1249-1927A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372170 | ||||||
chr7:151372210
|
A | G | 77 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(74): Show | 89 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1249-1887A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372210 | ||||||
chr7:151372221
|
C | A | 2 | a0001c0001t0008g0200a0001c0001t0008g0202 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1249-1876C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372221 | ||||||
chr7:151372243
|
C | T | 5 | a0001c0002t0001g0148a0001c0002t0001g0152a0001c0002t0001g0233others(2): Show | 5 | HG00639.hp1 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-1854C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372243 | ||||||
chr7:151372325
|
T | C | 252 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(249): Show | 275 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1249-1772T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372325 | ||||||
chr7:151372608
|
A | G | 266 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(263): Show | 289 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.1249-1489A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372608 | ||||||
chr7:151372648
|
G | A | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1249-1449G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372648 | ||||||
chr7:151372773
|
G | A | 10 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(7): Show | 10 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1249-1324G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372773 | ||||||
chr7:151372900
|
C | T | 1 | a0001c0002t0001g0030 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1249-1197C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372900 | ||||||
chr7:151372926
|
G | A | 1 | a0004c0010t0003g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1249-1171G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372926 | ||||||
chr7:151373121
|
G | A | 4 | a0001c0001t0002g0050a0001c0001t0002g0082a0001c0001t0002g0154others(1): Show | 4 | HG00323.hp2 HG01934.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-976G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373121 | ||||||
chr7:151373144
|
T | C | 4 | a0001c0002t0001g0060a0001c0002t0001g0119a0001c0002t0001g0125others(1): Show | 4 | NA18969.hp2 NA18971.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-953T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373144 | ||||||
chr7:151373207
|
T | C | 143 | a0001c0001t0003g0032a0001c0001t0003g0135a0001c0001t0003g0179others(140): Show | 149 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.1249-890T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373207 | ||||||
chr7:151373445
|
C | T | 134 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0258others(131): Show | 140 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1249-652C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373445 | ||||||
chr7:151373602
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1249-495G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373602 | ||||||
chr7:151373657
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1249-440T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373657 | ||||||
chr7:151373702
|
G | A | 5 | a0001c0002t0001g0147a0001c0002t0001g0290a0001c0002t0001g0291others(2): Show | 5 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-395G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373702 | ||||||
chr7:151373911
|
ACC | A | 4 | a0001c0001t0003g0205a0001c0001t0003g0209a0001c0001t0003g0273others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-183_1249-182d others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151373911 | |||||
chr7:151374257
|
C | T | 1 | a0001c0002t0001g0125 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1395+14C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374257 | ||||||
chr7:151374373
|
C | G | 1 | a0001c0001t0002g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1395+130C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374373 | ||||||
chr7:151374429
|
C | A | 1 | a0001c0001t0004g0375 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1395+186C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374429 | ||||||
chr7:151374540
|
G | A | 1 | a0001c0001t0003g0180 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1395+297G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374540 | ||||||
chr7:151374548
|
C | T | 1 | a0001c0003t0003g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1395+305C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374548 | ||||||
chr7:151374558
|
G | A | 1 | a0001c0002t0001g0016 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1395+315G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374558 | ||||||
chr7:151374652
|
C | A | 14 | a0001c0001t0003g0205a0001c0001t0003g0209a0001c0001t0003g0273others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395+409C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374652 | ||||||
chr7:151374753
|
T | A | 97 | a0001c0002t0001g0004a0001c0002t0001g0016a0001c0002t0001g0024others(94): Show | 102 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1395+510T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374753 | ||||||
chr7:151374796
|
C | T | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+553C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374796 | ||||||
chr7:151374797
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0136 | 2 | HG01257.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1395+554G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374797 | ||||||
chr7:151374801
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1395+558C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374801 | ||||||
chr7:151374840
|
C | T | 126 | a0001c0002t0001g0004a0001c0002t0001g0009a0001c0002t0001g0016others(123): Show | 132 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.1395+597C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374840 | ||||||
chr7:151374852
|
T | A | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+609T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374852 | ||||||
chr7:151374885
|
A | G | 261 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(258): Show | 284 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1395+642A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374885 | ||||||
chr7:151374962
|
G | A | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+719G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374962 | ||||||
chr7:151374978
|
A | G | 329 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(326): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1395+735A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374978 | ||||||
chr7:151375010
|
T | C | 2 | a0001c0005t0001g0183a0001c0005t0001g0275 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+767T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375010 | ||||||
chr7:151375022
|
G | A | 6 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+779G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375022 | ||||||
chr7:151375159
|
C | T | 1 | a0001c0001t0004g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1396-689C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375159 | ||||||
chr7:151375198
|
A | T | 3 | a0001c0001t0002g0139a0001c0001t0002g0199a0001c0003t0002g0035 | 3 | HG01109.hp1 HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1396-650A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375198 | ||||||
chr7:151375254
|
C | T | 329 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0002others(326): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1396-594C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375254 | ||||||
chr7:151375279
|
T | C | 12 | a0001c0001t0001g0367a0001c0001t0002g0001a0001c0001t0002g0042others(9): Show | 15 | HG01069.hp2 HG01070.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1396-569T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375279 | ||||||
chr7:151375326
|
A | G | 1 | a0001c0002t0001g0163 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1396-522A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375326 | ||||||
chr7:151375475
|
C | A | 1 | a0001c0001t0003g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1396-373C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375475 | ||||||
chr7:151375588
|
C | T | 2 | a0001c0004t0001g0116a0001c0004t0001g0214 | 2 | NA19012.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1396-260C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375588 | ||||||
chr7:151375792
|
TCTGA | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0288a0001c0001t0002g0317others(1): Show | 4 | HG02895.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-55_1396-52del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375792 | ||||||
chr7:151375793
|
C | G | 1 | a0001c0001t0004g0354 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1396-55C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375793 | ||||||
chr7:151376007
|
C | T | 67 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(64): Show | 77 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1491+64C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376007 | ||||||
chr7:151376035
|
A | T | 5 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0267others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1491+92A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376035 | ||||||
chr7:151376148
|
G | A | 7 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1491+205G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376148 | ||||||
chr7:151376312
|
A | G | 4 | a0001c0001t0003g0209a0001c0002t0001g0260a0001c0002t0001g0261others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1492-322A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376312 | ||||||
chr7:151376438
|
C | A | 4 | a0001c0001t0002g0139a0001c0001t0002g0288a0001c0001t0002g0318others(1): Show | 4 | HG01243.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492-196C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376438 | ||||||
chr7:151376484
|
T | C | 7 | a0001c0001t0007g0106a0001c0001t0007g0131a0001c0001t0007g0144others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1492-150T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376484 | ||||||
chr7:151376568
|
A | G | 6 | a0001c0001t0006g0008a0001c0001t0006g0022a0001c0001t0006g0025others(3): Show | 10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492-66A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376568 | ||||||
chr7:151376572
|
C | G | 117 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(114): Show | 130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1492-62C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376572 | ||||||
chr7:151376576
|
C | T | 11 | a0001c0002t0001g0009a0001c0002t0001g0068a0001c0002t0001g0093others(8): Show | 12 | NA18947.hp2 NA18951.hp2 NA18956.hp2 others(9): Show |
intron_variant | MODIFIER | c.1492-58C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376576 | ||||||
chr7:151376577
|
G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0145 | 2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1492-57G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376577 | ||||||
chr7:151376578
|
G | A | 3 | a0001c0001t0003g0209a0001c0001t0003g0273a0004c0010t0003g0208 | 3 | HG01884.hp1 HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1492-56G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376578 | ||||||
chr7:151376929
|
G | C | 131 | a0001c0001t0004g0287a0001c0001t0004g0329a0001c0001t0004g0356others(128): Show | 137 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.1669+118G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 14/14 | chr7 | 151376929 |