geneid | 4924 |
---|---|
ensemblid | ENSG00000104805.17 |
hgncid | 8043 |
symbol | NUCB1 |
name | nucleobindin 1 |
refseq_nuc | NM_006184.6 |
refseq_prot | NP_006175.2 |
ensembl_nuc | ENST00000405315.9 |
ensembl_prot | ENSP00000385923.3 |
mane_status | MANE Select |
chr | chr19 |
start | 48900312 |
end | 48923372 |
strand | + |
ver | v1.2 |
region | chr19:48900312-48923372 |
region5000 | chr19:48895312-48928372 |
regionname0 | NUCB1_chr19_48900312_48923372 |
regionname5000 | NUCB1_chr19_48895312_48928372 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 461 | 387 | 91 | 73 | 168 | 15 | 38 | 120 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0002 | 0/0 | 461 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0003 | 0/0 | 461 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0004 | 0/0 | 457 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0005 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0006 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1386 | 352 | 76 | 62 | 166 | 12 | 34 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0002 | 0/0 | 1386 | 15 | 1 | 9 | 0 | 3 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0003 | 0/0 | 1386 | 15 | 13 | 2 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0004 | 0/0 | 1386 | 7 | 7 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0005 | 0/0 | 1386 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0006 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0007 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0008 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0009 | 0/0 | 1374 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0010 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0011 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
c0012 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1021 | 199 | 67 | 19 | 97 | 2 | 14 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0002 | 0/1 | 1021 | 153 | 8 | 46 | 64 | 13 | 21 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0003 | 1/0 | 1021 | 15 | 3 | 2 | 7 | 0 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0004 | 0/0 | 1021 | 6 | 6 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0005 | 0/0 | 1021 | 5 | 0 | 3 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0006 | 0/0 | 1021 | 4 | 4 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0007 | 0/0 | 1021 | 4 | 0 | 3 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0008 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0009 | 0/0 | 1021 | 2 | 1 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0010 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0011 | 0/0 | 1021 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0012 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0013 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0014 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0015 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
t0016 | 0/0 | 1021 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1386 | 352 | 76 | 62 | 166 | 12 | 34 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0002 | 0/0 | 1386 | 15 | 1 | 9 | 0 | 3 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0003 | 0/0 | 1386 | 15 | 13 | 2 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0005 | 0/0 | 1386 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0007 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0008 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0011 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0002c0004 | 0/0 | 1386 | 7 | 7 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0003c0006 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0004c0009 | 0/0 | 1374 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0005c0010 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0006c0012 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2406 | 170 | 47 | 15 | 93 | 2 | 13 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0002 | 0/1 | 2406 | 140 | 7 | 40 | 64 | 10 | 18 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0003 | 1/0 | 2406 | 15 | 3 | 2 | 7 | 0 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0004 | 0/0 | 2406 | 6 | 6 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0005 | 0/0 | 2406 | 5 | 0 | 3 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0006 | 0/0 | 2406 | 4 | 4 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0007 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0008 | 0/0 | 2406 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0009 | 0/0 | 2406 | 2 | 1 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0010 | 0/0 | 2406 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0011 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0013 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0014 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0015 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0001t0016 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0002t0001 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0002t0002 | 0/0 | 2406 | 12 | 1 | 6 | 0 | 3 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0002t0007 | 0/0 | 2406 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0003t0001 | 0/0 | 2406 | 15 | 13 | 2 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0005t0001 | 0/0 | 2406 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0007t0001 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0008t0012 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0001c0011t0002 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0002c0004t0001 | 0/0 | 2406 | 7 | 7 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0003c0006t0007 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0004c0009t0001 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0005c0010t0001 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
a0006c0012t0001 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | copy fasta | chr19 | 48895312 | 48928372 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0002g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0007g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0009g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0009g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0014g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0001t0016g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0002t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0005t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0007t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0008t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0001c0011t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0002c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0002c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0002c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0002c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0002c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0002c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0002c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0003c0006t0007g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0004c0009t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0005c0010t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
a0006c0012t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0006 | t0007 | g0202 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0092 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | FIN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | FIN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0034 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG00741 | hp2 | a0001 | c0002 | t0007 | g0093 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0097 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0297 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0046 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0080 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01261 | hp1 | a0006 | c0012 | t0001 | g0339 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01358 | hp1 | a0001 | c0002 | t0007 | g0096 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0116 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0091 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0229 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0095 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0383 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0111 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0280 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0272 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0367 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0103 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02615 | hp2 | a0001 | c0001 | t0016 | g0340 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0376 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0184 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02717 | hp1 | a0002 | c0004 | t0001 | g0048 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0323 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0198 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0373 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02738 | hp2 | a0001 | c0011 | t0002 | g0336 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02809 | hp1 | a0001 | c0001 | t0015 | g0316 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0334 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02922 | hp2 | a0002 | c0004 | t0001 | g0032 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02965 | hp1 | a0001 | c0001 | t0013 | g0112 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0332 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02976 | hp2 | a0002 | c0004 | t0001 | g0059 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03041 | hp1 | a0001 | c0001 | t0014 | g0325 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0385 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03209 | hp2 | a0001 | c0008 | t0012 | g0020 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0337 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03669 | hp2 | a0001 | c0007 | t0001 | g0239 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0378 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0379 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03831 | hp1 | a0001 | c0001 | t0011 | g0299 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0351 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0377 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0368 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0372 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0374 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0380 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18522 | hp2 | a0002 | c0004 | t0001 | g0054 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0321 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0386 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0364 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0384 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0390 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18963 | hp1 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0387 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18992 | hp2 | a0004 | c0009 | t0001 | g0349 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0391 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0388 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19088 | hp1 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19091 | hp1 | a0005 | c0010 | t0001 | g0263 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA19240 | hp2 | a0002 | c0004 | t0001 | g0246 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20129 | hp1 | a0002 | c0004 | t0001 | g0041 | AFR | ASW | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | ASW | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0354 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0353 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0333 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02486 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0329 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0159 | REF | REF | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0138 | REF | REF | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48904438
|
A | G | 1 | a0006 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.227A>G | p.Asn76Ser | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/13 | 299/2406 | 227/1386 | 76/461 | chr19 | 48904438 | ||
chr19:48905769
|
G | A | 1 | a0003 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.260G>A | p.Arg87Gln | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/13 | 332/2406 | 260/1386 | 87/461 | chr19 | 48905769 | ||
chr19:48913164
|
C | T | 1 | a0005 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.634C>T | p.Arg212Trp | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/13 | 706/2406 | 634/1386 | 212/461 | chr19 | 48913164 | ||
chr19:48918759
|
A | C | 1 | a0004 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.791A>C | p.Glu264Ala | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/13 | 863/2406 | 791/1386 | 264/461 | chr19 | 48918759 | ||
chr19:48919268
|
C | A | 1 | a0004 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.984C>A | p.Asp328Glu | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/13 | 1056/2406 | 984/1386 | 328/461 | chr19 | 48919268 | ||
chr19:48919269
|
A | C | 1 | a0004 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.985A>C | p.Thr329Pro | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/13 | 1057/2406 | 985/1386 | 329/461 | chr19 | 48919269 | ||
chr19:48919270
|
C | A | 1 | a0004 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.986C>A | p.Thr329Asn | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/13 | 1058/2406 | 986/1386 | 329/461 | chr19 | 48919270 | ||
chr19:48921163
|
A | G | 1 | a0002 | 7 | HG02486.hp1 HG02717.hp1 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.1012A>G | p.Met338Val | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/13 | 1084/2406 | 1012/1386 | 338/461 | chr19 | 48921163 | ||
chr19:48921290
|
GCCGCCTG others(5): Show |
G | 1 | a0004 | 1 | NA18992.hp2 | disruptive_inframe_deletion | MODERATE | c.1142_1153delGCCTGG others(6): Show |
p.Arg381_Ala384del | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/13 | 1214/2406 | 1142/1386 | 381/461 | INFO_REALIGN_3_PRIME | chr19 | 48921290 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48904403
|
G | A | 1 | a0001c0002 | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
synonymous_variant | LOW | c.192G>A | p.Thr64Thr | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/13 | 264/2406 | 192/1386 | 64/461 | chr19 | 48904403 | ||
chr19:48913085
|
C | T | 1 | a0001c0011 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.555C>T | p.His185His | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/13 | 627/2406 | 555/1386 | 185/461 | chr19 | 48913085 | ||
chr19:48913136
|
G | A | 1 | a0001c0007 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.606G>A | p.Ala202Ala | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/13 | 678/2406 | 606/1386 | 202/461 | chr19 | 48913136 | ||
chr19:48921177
|
C | T | 1 | a0001c0005 | 2 | NA18963.hp1 NA19088.hp1 |
synonymous_variant | LOW | c.1026C>T | p.Tyr342Tyr | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/13 | 1098/2406 | 1026/1386 | 342/461 | chr19 | 48921177 | ||
chr19:48922319
|
C | T | 1 | a0001c0003 | 15 | HG00733.hp2 HG01433.hp1 HG01891.hp2 others(12): Show |
splice_region_variant&synonymous_variant | LOW | c.1281C>T | p.Asp427Asp | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 1353/2406 | 1281/1386 | 427/461 | chr19 | 48922319 | ||
chr19:48922394
|
C | G | 1 | a0001c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1356C>G | p.Leu452Leu | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 1428/2406 | 1356/1386 | 452/461 | chr19 | 48922394 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48922515
|
T | C | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(23): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
3_prime_UTR_variant | MODIFIER | c.*91T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 91 | chr19 | 48922515 | |||||
chr19:48922563
|
G | A | 1 | a0001c0001t0008 | 2 | HG02559.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 139 | chr19 | 48922563 | |||||
chr19:48922581
|
G | A | 4 | a0001c0001t0002a0001c0001t0011a0001c0002t0002others(1): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*157G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 157 | chr19 | 48922581 | |||||
chr19:48922703
|
G | A | 1 | a0001c0001t0011 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 279 | chr19 | 48922703 | |||||
chr19:48922708
|
C | T | 1 | a0001c0001t0016 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 284 | chr19 | 48922708 | |||||
chr19:48922765
|
T | C | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 13 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*341T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 341 | chr19 | 48922765 | |||||
chr19:48922808
|
T | G | 1 | a0001c0001t0008 | 2 | HG02559.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*384T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 384 | chr19 | 48922808 | |||||
chr19:48922823
|
G | T | 1 | a0001c0001t0009 | 2 | HG01243.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*399G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 399 | chr19 | 48922823 | |||||
chr19:48922842
|
G | A | 4 | a0001c0001t0002a0001c0001t0011a0001c0002t0002others(1): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 418 | chr19 | 48922842 | |||||
chr19:48923092
|
C | G | 1 | a0001c0001t0015 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 668 | chr19 | 48923092 | |||||
chr19:48923139
|
C | G | 1 | a0001c0001t0005 | 5 | HG01257.hp1 HG02148.hp1 HG02148.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*715C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 715 | chr19 | 48923139 | |||||
chr19:48923209
|
C | T | 1 | a0001c0001t0014 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 785 | chr19 | 48923209 | |||||
chr19:48923210
|
G | A | 1 | a0001c0001t0006 | 4 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*786G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 786 | chr19 | 48923210 | |||||
chr19:48923230
|
T | C | 1 | a0001c0008t0012 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 806 | chr19 | 48923230 | |||||
chr19:48923231
|
T | C | 3 | a0001c0001t0007a0001c0002t0007a0003c0006t0007 | 4 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*807T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 807 | chr19 | 48923231 | |||||
chr19:48923241
|
G | A | 1 | a0001c0008t0012 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 817 | chr19 | 48923241 | |||||
chr19:48923289
|
G | A | 1 | a0001c0001t0013 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 865 | chr19 | 48923289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:48900420
|
G | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(79): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-12+48G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900420 | ||||||
chr19:48900617
|
C | T | 3 | a0001c0001t0001g0389a0001c0001t0001g0391a0001c0001t0002g0390 | 3 | NA18962.hp1 NA19012.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-11-169C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900617 | ||||||
chr19:48900731
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-11-55G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900731 | ||||||
chr19:48900765
|
C | G | 3 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0001t0001g0388 | 3 | NA18950.hp2 NA18977.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-11-21C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900765 | ||||||
chr19:48900956
|
A | G | 1 | a0001c0001t0001g0385 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.135+25A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48900956 | ||||||
chr19:48901011
|
G | T | 1 | a0001c0001t0003g0384 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.135+80G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901011 | ||||||
chr19:48901110
|
CCTGACT | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0342others(42): Show | 47 | HG00621.hp2 HG01993.hp2 HG02071.hp1 others(44): Show |
intron_variant | MODIFIER | c.135+184_135+189del others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48901110 | |||||
chr19:48901136
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(79): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.135+205C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901136 | ||||||
chr19:48901191
|
A | T | 3 | a0001c0001t0001g0341a0001c0001t0016g0340a0006c0012t0001g0339 | 3 | HG01261.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.135+260A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901191 | ||||||
chr19:48901278
|
T | G | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+347T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901278 | ||||||
chr19:48901327
|
C | T | 3 | a0001c0001t0001g0338a0001c0003t0001g0337a0001c0011t0002g0336 | 3 | HG02280.hp1 HG02738.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.135+396C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901327 | ||||||
chr19:48901958
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.135+1027C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901958 | ||||||
chr19:48902255
|
C | T | 1 | a0001c0001t0002g0335 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.135+1324C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902255 | ||||||
chr19:48902311
|
A | G | 25 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(22): Show | 25 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.135+1380A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902311 | ||||||
chr19:48902412
|
TCCTTTTT others(1): Show |
T | 24 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(21): Show | 24 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+1482_135+1489d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902412 | ||||||
chr19:48902413
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(92): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.135+1482C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902413 | ||||||
chr19:48902420
|
CT | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.135+1507delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902420 | |||||
chr19:48902420
|
CTT | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0104a0001c0001t0002g0015others(16): Show | 19 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.135+1506_135+1507d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902420 | |||||
chr19:48902422
|
T | C | 24 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(21): Show | 24 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+1491T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902422 | ||||||
chr19:48902423
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+1492T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902423 | ||||||
chr19:48902425
|
T | C | 6 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0109others(3): Show | 6 | NA18955.hp2 NA18960.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+1494T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902425 | ||||||
chr19:48902438
|
T | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+1507T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902438 | ||||||
chr19:48902478
|
A | G | 1 | a0001c0001t0004g0334 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+1547A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902478 | ||||||
chr19:48902768
|
C | T | 1 | a0001c0001t0004g0333 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-1579C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902768 | ||||||
chr19:48902879
|
G | C | 25 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(22): Show | 25 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.136-1468G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902879 | ||||||
chr19:48902918
|
A | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.136-1429A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902918 | ||||||
chr19:48902937
|
G | GTA | 26 | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0001g0311others(23): Show | 26 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.136-1394_136-1393d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | |||||
chr19:48902937
|
G | GTATA | 97 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(94): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.136-1396_136-1393d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | |||||
chr19:48902937
|
G | GTATATA | 33 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(30): Show | 35 | HG00621.hp2 HG01891.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.136-1398_136-1393d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | |||||
chr19:48902937
|
G | GTATATAT others(1): Show |
12 | a0001c0001t0001g0088a0001c0001t0001g0342a0001c0001t0001g0343others(9): Show | 12 | HG02071.hp1 HG02132.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-1400_136-1393d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | |||||
chr19:48902956
|
T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0113others(47): Show | 52 | HG00621.hp2 HG01993.hp2 HG02071.hp1 others(49): Show |
intron_variant | MODIFIER | c.136-1391T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902956 | ||||||
chr19:48903376
|
G | GGTGTAGA others(10): Show |
1 | a0001c0002t0002g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136-970_136-969ins others(17): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903376 | |||||
chr19:48903380
|
A | AGATGGAT others(9): Show |
15 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(12): Show | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-954_136-953ins others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903380 | |||||
chr19:48903380
|
A | G | 1 | a0001c0002t0002g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136-967A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903380 | ||||||
chr19:48903392
|
A | AGGTGGAT others(9): Show |
104 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(101): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.136-954_136-953ins others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903392 | |||||
chr19:48903394
|
T | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.136-953T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903394 | ||||||
chr19:48903408
|
G | A | 1 | a0001c0001t0003g0372 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.136-939G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903408 | ||||||
chr19:48903450
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(72): Show | 77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.136-897A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903450 | ||||||
chr19:48903454
|
G | A | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-893G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903454 | ||||||
chr19:48903458
|
T | TTGGATGG others(9): Show |
1 | a0001c0001t0002g0105 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136-860_136-845dup others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903458 | |||||
chr19:48903471
|
C | T | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-876C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903471 | ||||||
chr19:48903474
|
G | T | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-873G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903474 | ||||||
chr19:48903524
|
G | GGATGGGT others(13): Show |
1 | a0001c0001t0002g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136-803_136-784dup others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903524 | |||||
chr19:48903533
|
G | T | 1 | a0001c0001t0002g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.136-814G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903533 | ||||||
chr19:48903544
|
C | G | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-803C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903544 | ||||||
chr19:48903569
|
A | G | 3 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG01070.hp2 HG01071.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.136-778A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903569 | ||||||
chr19:48903590
|
A | G | 1 | a0001c0001t0001g0371 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.136-757A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903590 | ||||||
chr19:48903647
|
C | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.136-700C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903647 | ||||||
chr19:48903673
|
AGTGGATG others(13): Show |
A | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.136-638_136-619del others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903673 | |||||
chr19:48903718
|
A | G | 52 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0113others(49): Show | 54 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-629A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903718 | ||||||
chr19:48903828
|
A | G | 1 | a0001c0001t0002g0310 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.136-519A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903828 | ||||||
chr19:48903858
|
GTGGA | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(175): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.136-465_136-462del others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903858 | |||||
chr19:48903858
|
GTGGATGG others(1): Show |
G | 78 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(75): Show | 80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.136-469_136-462del others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903858 | |||||
chr19:48903882
|
A | ATGGG | 75 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(72): Show | 77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.136-457_136-454dup others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903882 | |||||
chr19:48903882
|
A | G | 105 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0088others(102): Show | 107 | HG00140.hp2 HG00621.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-465A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903882 | ||||||
chr19:48903894
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.136-453A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903894 | ||||||
chr19:48903956
|
GGATGGGT others(16): Show |
G | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.136-379_136-357del others(23): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903956 | |||||
chr19:48903966
|
A | G | 1 | a0001c0001t0002g0309 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.136-381A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903966 | ||||||
chr19:48903982
|
T | C | 55 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0113others(52): Show | 57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.136-365T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903982 | ||||||
chr19:48903987
|
G | GGATA | 4 | a0001c0001t0001g0315a0001c0001t0001g0317a0001c0001t0001g0318others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-356_136-353dup others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903987 | |||||
chr19:48904102
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.136-245G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48904102 | ||||||
chr19:48904111
|
A | C | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.136-236A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48904111 | ||||||
chr19:48904148
|
T | C | 1 | a0001c0001t0004g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136-199T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48904148 | ||||||
chr19:48904458
|
C | T | 15 | a0001c0002t0001g0098a0001c0002t0002g0089a0001c0002t0002g0090others(12): Show | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.243+4C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904458 | ||||||
chr19:48904476
|
C | T | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+22C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904476 | ||||||
chr19:48904490
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.243+36C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904490 | ||||||
chr19:48904522
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.243+68G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904522 | ||||||
chr19:48904527
|
C | CT | 36 | a0001c0001t0001g0083a0001c0001t0001g0119a0001c0001t0001g0120others(33): Show | 36 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.243+88dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 48904527 | |||||
chr19:48904587
|
C | T | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.243+133C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904587 | ||||||
chr19:48904669
|
G | A | 1 | a0001c0001t0005g0156 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.243+215G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904669 | ||||||
chr19:48904690
|
A | G | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+236A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904690 | ||||||
chr19:48904758
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.243+304G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904758 | ||||||
chr19:48904765
|
T | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.243+311T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904765 | ||||||
chr19:48904972
|
TG | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.243+521delG | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 48904972 | |||||
chr19:48904988
|
C | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0013g0112others(2): Show | 5 | HG01433.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+534C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904988 | ||||||
chr19:48905046
|
C | T | 360 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(357): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.243+592C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905046 | ||||||
chr19:48905101
|
C | G | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+647C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905101 | ||||||
chr19:48905144
|
G | C | 2 | a0001c0001t0001g0030a0001c0001t0002g0029 | 2 | HG01106.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.244-609G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905144 | ||||||
chr19:48905410
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244-343G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905410 | ||||||
chr19:48905642
|
A | G | 1 | a0001c0001t0005g0080 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.244-111A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905642 | ||||||
chr19:48905686
|
T | C | 15 | a0001c0002t0001g0098a0001c0002t0002g0089a0001c0002t0002g0090others(12): Show | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.244-67T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905686 | ||||||
chr19:48905747
|
T | C | 16 | a0001c0001t0001g0104a0001c0002t0001g0098a0001c0002t0002g0089others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.244-6T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905747 | ||||||
chr19:48905940
|
TCACTC | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(76): Show | 81 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+57_376+61delAC others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48905940 | |||||
chr19:48905964
|
TGTGCTAG others(4): Show |
T | 79 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(76): Show | 81 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+83_376+93delCT others(9): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48905964 | |||||
chr19:48905994
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.376+109C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48905994 | ||||||
chr19:48906017
|
G | A | 3 | a0001c0001t0001g0341a0001c0001t0016g0340a0006c0012t0001g0339 | 3 | HG01261.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.376+132G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906017 | ||||||
chr19:48906175
|
G | T | 1 | a0001c0001t0002g0304 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+290G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906175 | ||||||
chr19:48906196
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.376+311G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906196 | ||||||
chr19:48906211
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(157): Show | 164 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.376+326T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906211 | ||||||
chr19:48906368
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.376+483C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906368 | ||||||
chr19:48906390
|
T | G | 1 | a0001c0001t0002g0157 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.376+505T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906390 | ||||||
chr19:48906403
|
C | CA | 13 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0161others(10): Show | 13 | HG00438.hp1 HG01074.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.376+536dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906403 | |||||
chr19:48906403
|
C | CAA | 148 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(145): Show | 152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.376+535_376+536dup others(2): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906403 | |||||
chr19:48906403
|
C | CAAA | 9 | a0001c0001t0001g0088a0001c0001t0001g0113a0001c0001t0001g0341others(6): Show | 9 | HG01261.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.376+534_376+536dup others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906403 | |||||
chr19:48906535
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.376+650A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906535 | ||||||
chr19:48906929
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.376+1044C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906929 | ||||||
chr19:48906934
|
G | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(118): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.376+1049G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906934 | ||||||
chr19:48906950
|
C | G | 4 | a0001c0001t0001g0368a0001c0001t0001g0383a0001c0001t0002g0351others(1): Show | 4 | HG01993.hp2 HG02300.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+1065C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906950 | ||||||
chr19:48906979
|
C | CT | 157 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(154): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.376+1107dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906979 | |||||
chr19:48906998
|
A | G | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.376+1113A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906998 | ||||||
chr19:48907005
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01123.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.376+1120C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907005 | ||||||
chr19:48907040
|
T | C | 55 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0113others(52): Show | 57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1155T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907040 | ||||||
chr19:48907216
|
G | T | 39 | a0001c0001t0001g0104a0001c0001t0001g0311a0001c0001t0001g0312others(36): Show | 39 | HG00140.hp2 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.376+1331G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907216 | ||||||
chr19:48907272
|
C | CT | 31 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0001g0153others(28): Show | 31 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.376+1405dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48907272 | |||||
chr19:48907289
|
T | C | 1 | a0001c0001t0002g0031 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.376+1404T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907289 | ||||||
chr19:48907338
|
C | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0113others(52): Show | 57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1453C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907338 | ||||||
chr19:48907417
|
A | G | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.376+1532A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907417 | ||||||
chr19:48907615
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.376+1730C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907615 | ||||||
chr19:48907663
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.376+1778G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907663 | ||||||
chr19:48907713
|
T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(178): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.376+1828T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907713 | ||||||
chr19:48907743
|
C | A | 1 | a0001c0001t0002g0133 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.376+1858C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907743 | ||||||
chr19:48907769
|
G | A | 3 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0001t0001g0388 | 3 | NA18950.hp2 NA18977.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.376+1884G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907769 | ||||||
chr19:48907775
|
A | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0113others(52): Show | 57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1890A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907775 | ||||||
chr19:48907822
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+1937G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907822 | ||||||
chr19:48907841
|
G | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(173): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.376+1956G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907841 | ||||||
chr19:48907914
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.376+2029C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907914 | ||||||
chr19:48907941
|
T | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0131others(23): Show | 27 | HG00408.hp2 HG00621.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.376+2056T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907941 | ||||||
chr19:48908033
|
G | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.376+2148G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908033 | ||||||
chr19:48908303
|
T | C | 15 | a0001c0002t0001g0098a0001c0002t0002g0089a0001c0002t0002g0090others(12): Show | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.376+2418T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908303 | ||||||
chr19:48908311
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.376+2426G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908311 | ||||||
chr19:48908329
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.376+2444C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908329 | ||||||
chr19:48908604
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0008g0178 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.377-2545G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908604 | ||||||
chr19:48908648
|
C | CGT | 38 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0038others(35): Show | 39 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.377-2452_377-2451d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGT | 57 | a0001c0001t0001g0017a0001c0001t0001g0047a0001c0001t0001g0050others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.377-2454_377-2451d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGT | 54 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0055others(51): Show | 54 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.377-2456_377-2451d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGTG others(1): Show |
35 | a0001c0001t0001g0058a0001c0001t0001g0119a0001c0001t0001g0134others(32): Show | 35 | HG00423.hp2 HG00642.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.377-2458_377-2451d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGTG others(3): Show |
36 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(33): Show | 38 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.377-2460_377-2451d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGTG others(5): Show |
27 | a0001c0001t0001g0069a0001c0001t0001g0110a0001c0001t0001g0117others(24): Show | 27 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.377-2462_377-2451d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGTG others(7): Show |
17 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0104others(14): Show | 18 | HG00408.hp1 HG01255.hp1 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.377-2464_377-2451d others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGTG others(9): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0131others(10): Show | 14 | HG00408.hp2 HG00544.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.377-2466_377-2451d others(18): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGTG others(11): Show |
4 | a0001c0001t0001g0075a0001c0001t0001g0289a0001c0001t0001g0391others(1): Show | 4 | HG01258.hp1 NA18999.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2468_377-2451d others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CGTGTGTG others(13): Show |
1 | a0001c0001t0002g0290 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.377-2470_377-2451d others(22): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
C | CTGTGTGT others(10): Show |
1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.377-2501_377-2500i others(19): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908648 | ||||||
chr19:48908648
|
CGT | C | 25 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0001g0185others(22): Show | 25 | HG00621.hp2 HG01123.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.377-2452_377-2451d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
CGTGT | C | 11 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(8): Show | 11 | HG02055.hp2 HG02155.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.377-2454_377-2451d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
CGTGTGT | C | 6 | a0001c0001t0001g0180a0001c0001t0001g0383a0001c0001t0002g0181others(3): Show | 6 | HG00438.hp2 HG00609.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-2456_377-2451d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
CGTGTGTG others(3): Show |
C | 2 | a0001c0002t0001g0098a0001c0002t0002g0099 | 2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.377-2460_377-2451d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
CGTGTGTG others(5): Show |
C | 13 | a0001c0001t0001g0115a0001c0002t0002g0089a0001c0002t0002g0090others(10): Show | 13 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.377-2462_377-2451d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0002g0152a0002c0004t0001g0032 | 2 | HG02922.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.377-2464_377-2451d others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908648
|
CGTGTGTG others(23): Show |
C | 1 | a0001c0001t0002g0375 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.377-2480_377-2451d others(32): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | |||||
chr19:48908718
|
A | AGG | 34 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0021others(31): Show | 35 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.377-2428_377-2427d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908718 | |||||
chr19:48908719
|
G | GGGGT | 23 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0124others(20): Show | 25 | HG00621.hp2 HG02055.hp2 HG02622.hp2 others(22): Show |
intron_variant | MODIFIER | c.377-2428_377-2425d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908719 | |||||
chr19:48908721
|
G | GGGGT | 18 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0002g0060others(15): Show | 18 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.377-2427_377-2426i others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGGGTGTG others(3): Show |
1 | a0001c0002t0002g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.377-2427_377-2426i others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGT | 61 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0036others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.377-2387_377-2386d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGGT | 4 | a0001c0001t0001g0379a0001c0001t0002g0353a0001c0001t0002g0354others(1): Show | 4 | HG03710.hp2 NA19083.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGGTG others(1): Show |
9 | a0001c0001t0001g0125a0001c0001t0001g0347a0001c0001t0001g0383others(6): Show | 9 | HG01993.hp2 HG02132.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGGTG others(3): Show |
4 | a0001c0001t0001g0088a0001c0001t0001g0348a0001c0001t0001g0368others(1): Show | 4 | HG03831.hp2 HG03942.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGGTG others(5): Show |
3 | a0001c0001t0001g0342a0001c0001t0001g0345a0001c0001t0002g0352 | 3 | NA18747.hp1 NA18955.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.377-2425_377-2424i others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGGTG others(7): Show |
2 | a0001c0001t0001g0343a0001c0001t0002g0358 | 2 | HG02155.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.377-2425_377-2424i others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGGTG others(9): Show |
1 | a0001c0001t0001g0350 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.377-2425_377-2424i others(18): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGGTG others(11): Show |
1 | a0001c0001t0001g0344 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.377-2425_377-2424i others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGGTGT others(4): Show |
1 | a0001c0001t0001g0346 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.377-2425_377-2424i others(13): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGT | 18 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0079others(15): Show | 19 | HG00423.hp1 HG01255.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-2389_377-2386d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGTGT | 9 | a0001c0001t0001g0005a0001c0001t0001g0233a0001c0001t0002g0164others(6): Show | 10 | HG00597.hp2 HG01358.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.377-2391_377-2386d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGTGTG others(1): Show |
7 | a0001c0002t0001g0098a0001c0002t0002g0091a0001c0002t0002g0092others(4): Show | 7 | HG00140.hp2 HG00741.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.377-2393_377-2386d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGTGTG others(3): Show |
3 | a0001c0002t0002g0099a0001c0002t0002g0101a0001c0002t0007g0096 | 3 | HG01109.hp1 HG01192.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.377-2395_377-2386d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GGTGTGTG others(5): Show |
1 | a0001c0002t0002g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.377-2397_377-2386d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
G | GT | 4 | a0001c0001t0001g0131a0001c0001t0001g0251a0001c0001t0001g0319others(1): Show | 4 | HG01255.hp2 HG02523.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2428_377-2427i others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908721 | ||||||
chr19:48908721
|
G | GTGTGT | 3 | a0001c0001t0002g0264a0001c0001t0005g0272a0001c0001t0005g0280 | 3 | HG02148.hp1 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.377-2428_377-2427i others(7): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908721 | ||||||
chr19:48908721
|
GGT | G | 12 | a0001c0001t0001g0050a0001c0001t0001g0180a0001c0001t0001g0284others(9): Show | 12 | HG00609.hp1 HG01256.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.377-2387_377-2386d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
GGTGT | G | 22 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0001g0170others(19): Show | 22 | HG00140.hp1 HG00733.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.377-2389_377-2386d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
GGTGTGT | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG00438.hp1 HG01106.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-2391_377-2386d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908721
|
GGTGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0341a0001c0001t0016g0340a0006c0012t0001g0339 | 3 | HG01261.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.377-2397_377-2386d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | |||||
chr19:48908723
|
T | G | 12 | a0001c0001t0001g0208a0001c0001t0001g0235a0001c0001t0001g0315others(9): Show | 12 | HG00558.hp1 HG01978.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.377-2426T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908723 | ||||||
chr19:48908723
|
T | TGG | 4 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0369others(1): Show | 4 | HG02896.hp2 HG02897.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908723 | |||||
chr19:48908725
|
T | G | 2 | a0001c0001t0001g0338a0001c0011t0002g0336 | 2 | HG02280.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.377-2424T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908725 | ||||||
chr19:48908844
|
C | A | 15 | a0001c0002t0001g0098a0001c0002t0002g0089a0001c0002t0002g0090others(12): Show | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.377-2305C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908844 | ||||||
chr19:48909142
|
T | G | 1 | a0001c0001t0001g0320 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.377-2007T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909142 | ||||||
chr19:48909248
|
TA | T | 23 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0311others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.377-1900delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909248 | ||||||
chr19:48909249
|
A | T | 7 | a0001c0001t0001g0248a0001c0001t0001g0287a0001c0001t0001g0300others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-1900A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909249 | ||||||
chr19:48909249
|
AT | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(76): Show | 81 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.377-1887delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48909249 | |||||
chr19:48909252
|
T | A | 23 | a0001c0001t0001g0170a0001c0001t0001g0201a0001c0001t0002g0147others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.377-1897T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909252 | ||||||
chr19:48909253
|
T | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0043others(6): Show | 9 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1896T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909253 | ||||||
chr19:48909255
|
T | A | 15 | a0001c0002t0001g0098a0001c0002t0002g0089a0001c0002t0002g0090others(12): Show | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.377-1894T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909255 | ||||||
chr19:48909261
|
T | C | 4 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0385others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-1888T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909261 | ||||||
chr19:48909262
|
T | C | 26 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0001g0120others(23): Show | 26 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.377-1887T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909262 | ||||||
chr19:48909283
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0002g0023a0001c0001t0010g0027others(8): Show | 12 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.377-1866C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909283 | ||||||
chr19:48909396
|
C | T | 1 | a0001c0001t0001g0377 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.377-1753C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909396 | ||||||
chr19:48909447
|
A | G | 2 | a0001c0001t0002g0373a0001c0001t0002g0378 | 2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.377-1702A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909447 | ||||||
chr19:48909568
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.377-1581T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909568 | ||||||
chr19:48909580
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.377-1569C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909580 | ||||||
chr19:48909752
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.377-1397C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909752 | ||||||
chr19:48909931
|
A | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0042 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.377-1218A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909931 | ||||||
chr19:48909979
|
T | C | 23 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.377-1170T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909979 | ||||||
chr19:48910002
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(159): Show | 166 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.377-1147T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910002 | ||||||
chr19:48910073
|
G | A | 3 | a0001c0001t0002g0128a0001c0001t0002g0155a0001c0001t0002g0274 | 3 | HG00733.hp1 HG01256.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.377-1076G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910073 | ||||||
chr19:48910102
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.377-1047C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910102 | ||||||
chr19:48910242
|
A | G | 1 | a0001c0003t0001g0337 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.377-907A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910242 | ||||||
chr19:48910368
|
A | G | 6 | a0002c0004t0001g0032a0002c0004t0001g0040a0002c0004t0001g0041others(3): Show | 6 | HG02486.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-781A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910368 | ||||||
chr19:48910382
|
GT | G | 390 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(387): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.377-759delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48910382 | |||||
chr19:48910405
|
G | A | 19 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0212others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-744G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910405 | ||||||
chr19:48910562
|
T | C | 19 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0212others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-587T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910562 | ||||||
chr19:48910634
|
G | A | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(6): Show | 9 | HG01346.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-515G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910634 | ||||||
chr19:48910665
|
C | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0013g0112others(2): Show | 5 | HG01433.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-484C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910665 | ||||||
chr19:48910672
|
CA | C | 9 | a0001c0001t0001g0289a0001c0001t0001g0314a0001c0001t0001g0344others(6): Show | 9 | HG01070.hp2 HG01257.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-462delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48910672 | |||||
chr19:48911328
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0013g0112others(2): Show | 5 | HG01433.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+76G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911328 | ||||||
chr19:48911385
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.480+133T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911385 | ||||||
chr19:48911391
|
GTTTCT | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(66): Show | 71 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.480+153_480+157del others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48911391 | |||||
chr19:48911405
|
C | CT | 13 | a0001c0001t0001g0066a0001c0001t0001g0119a0001c0001t0001g0120others(10): Show | 13 | HG01255.hp1 HG01346.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.480+170dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48911405 | |||||
chr19:48911405
|
CT | C | 57 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0104others(54): Show | 59 | HG00621.hp2 HG00642.hp1 HG01261.hp2 others(56): Show |
intron_variant | MODIFIER | c.480+170delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48911405 | |||||
chr19:48911475
|
G | A | 56 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0338others(53): Show | 58 | HG00621.hp2 HG00642.hp1 HG01261.hp2 others(55): Show |
intron_variant | MODIFIER | c.480+223G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911475 | ||||||
chr19:48911562
|
C | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0119a0001c0001t0001g0120others(7): Show | 10 | HG01346.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+310C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911562 | ||||||
chr19:48911639
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0013g0112 | 2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.480+387C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911639 | ||||||
chr19:48911874
|
C | T | 19 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0212others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+622C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911874 | ||||||
chr19:48911993
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.480+741C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911993 | ||||||
chr19:48912019
|
C | CT | 19 | a0001c0001t0001g0012a0001c0001t0001g0211a0001c0001t0001g0385others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+786dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912019 | |||||
chr19:48912019
|
CT | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(148): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.480+786delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912019 | |||||
chr19:48912104
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.480+852A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912104 | ||||||
chr19:48912129
|
A | G | 1 | a0001c0001t0009g0332 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.480+877A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912129 | ||||||
chr19:48912179
|
C | T | 16 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0212others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.481-832C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912179 | ||||||
chr19:48912225
|
T | C | 20 | a0001c0001t0001g0113a0001c0001t0001g0123a0001c0001t0001g0124others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.481-786T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912225 | ||||||
chr19:48912311
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.481-700C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912311 | ||||||
chr19:48912377
|
G | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(70): Show | 75 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.481-634G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912377 | ||||||
chr19:48912561
|
C | T | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.481-450C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912561 | ||||||
chr19:48912604
|
C | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(100): Show | 106 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.481-407C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912604 | ||||||
chr19:48912627
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.481-384G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912627 | ||||||
chr19:48912665
|
G | A | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.481-346G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912665 | ||||||
chr19:48912704
|
C | T | 1 | a0001c0001t0001g0391 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.481-307C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912704 | ||||||
chr19:48912711
|
C | T | 1 | a0001c0001t0002g0367 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.481-300C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912711 | ||||||
chr19:48912714
|
T | TA | 27 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0119others(24): Show | 27 | HG00140.hp2 HG00280.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.481-295dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912714 | |||||
chr19:48912760
|
C | T | 1 | a0001c0001t0005g0193 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.481-251C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912760 | ||||||
chr19:48912843
|
C | CA | 49 | a0001c0001t0001g0007a0001c0001t0001g0083a0001c0001t0001g0123others(46): Show | 51 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.481-149dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | |||||
chr19:48912843
|
C | CAA | 14 | a0001c0001t0001g0021a0001c0001t0001g0087a0001c0001t0001g0104others(11): Show | 14 | HG01433.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.481-150_481-149dup others(2): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | |||||
chr19:48912843
|
C | CAAA | 28 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0042others(25): Show | 28 | HG00733.hp2 HG01070.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.481-151_481-149dup others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | |||||
chr19:48912843
|
C | CAAAA | 13 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0119others(10): Show | 13 | HG01346.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-152_481-149dup others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | |||||
chr19:48912843
|
CA | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(87): Show | 93 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.481-149delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | |||||
chr19:48912914
|
C | T | 2 | a0001c0002t0002g0089a0001c0002t0002g0103 | 2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.481-97C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912914 | ||||||
chr19:48913199
|
G | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
splice_region_variant&intron_variant | LOW | c.666+3G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913199 | ||||||
chr19:48913208
|
A | G | 1 | a0001c0001t0002g0375 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.666+12A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913208 | ||||||
chr19:48913246
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.666+50C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913246 | ||||||
chr19:48913247
|
G | C | 13 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0119others(10): Show | 13 | HG01255.hp2 HG01346.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.666+51G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913247 | ||||||
chr19:48913297
|
C | CA | 7 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+108dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 48913297 | |||||
chr19:48913297
|
CA | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.666+108delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 48913297 | |||||
chr19:48913679
|
C | T | 89 | a0001c0001t0001g0042a0001c0001t0001g0123a0001c0001t0001g0124others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.757+115C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913679 | ||||||
chr19:48913723
|
G | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+159G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913723 | ||||||
chr19:48913731
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0072 | 2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.757+167G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913731 | ||||||
chr19:48913817
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0033others(32): Show | 36 | HG00544.hp1 HG00642.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.757+253G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913817 | ||||||
chr19:48913941
|
G | C | 3 | a0001c0001t0004g0158a0001c0001t0004g0334a0001c0008t0012g0020 | 3 | HG02809.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.757+377G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913941 | ||||||
chr19:48913968
|
C | CT | 30 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0134others(27): Show | 30 | HG00621.hp1 HG00673.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.757+421dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48913968 | |||||
chr19:48913971
|
T | C | 1 | a0001c0001t0004g0329 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.757+407T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913971 | ||||||
chr19:48913989
|
A | G | 171 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0042others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.757+425A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913989 | ||||||
chr19:48914068
|
C | T | 13 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0079others(10): Show | 13 | HG01261.hp1 HG01433.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.757+504C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914068 | ||||||
chr19:48914173
|
A | T | 1 | a0001c0001t0002g0295 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.757+609A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914173 | ||||||
chr19:48914230
|
A | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(214): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.757+666A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914230 | ||||||
chr19:48914267
|
G | A | 2 | a0001c0001t0001g0311a0001c0001t0001g0327 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.757+703G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914267 | ||||||
chr19:48914401
|
T | C | 369 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(366): Show | 376 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(373): Show |
intron_variant | MODIFIER | c.757+837T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914401 | ||||||
chr19:48914432
|
C | G | 6 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0114others(3): Show | 6 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+868C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914432 | ||||||
chr19:48914528
|
C | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0341a0001c0001t0010g0184others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.757+964C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914528 | ||||||
chr19:48914616
|
G | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0114others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+1052G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914616 | ||||||
chr19:48914684
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(234): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.757+1120T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914684 | ||||||
chr19:48914784
|
T | TA | 9 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0002g0365others(6): Show | 9 | HG01109.hp1 HG01433.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.757+1232dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48914784 | |||||
chr19:48914796
|
AT | A | 5 | a0001c0001t0002g0077a0001c0001t0002g0136a0001c0001t0002g0183others(2): Show | 5 | HG01123.hp2 HG01981.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.757+1233delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914796 | ||||||
chr19:48914797
|
T | A | 182 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0042others(179): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.757+1233T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914797 | ||||||
chr19:48914876
|
T | G | 2 | a0001c0001t0002g0288a0001c0001t0002g0290 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.757+1312T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914876 | ||||||
chr19:48914886
|
G | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0386 | 2 | NA18747.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.757+1322G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914886 | ||||||
chr19:48914934
|
G | T | 2 | a0001c0003t0001g0111a0001c0003t0001g0321 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.757+1370G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914934 | ||||||
chr19:48914981
|
G | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0119a0001c0001t0001g0120others(11): Show | 14 | HG01346.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.757+1417G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914981 | ||||||
chr19:48915007
|
G | A | 7 | a0001c0001t0002g0023a0001c0001t0002g0160a0001c0001t0002g0167others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.757+1443G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915007 | ||||||
chr19:48915111
|
G | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0114others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+1547G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915111 | ||||||
chr19:48915333
|
A | AAAAAC | 249 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(246): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.757+1779_757+1783d others(7): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48915333 | |||||
chr19:48915340
|
A | AAAC | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 136 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.757+1779_757+1781d others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48915340 | |||||
chr19:48915403
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(232): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.757+1839T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915403 | ||||||
chr19:48915429
|
C | T | 3 | a0001c0001t0001g0341a0001c0001t0010g0184a0001c0001t0016g0340 | 3 | HG02257.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.757+1865C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915429 | ||||||
chr19:48915451
|
G | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0033others(34): Show | 38 | HG00140.hp2 HG00544.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.757+1887G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915451 | ||||||
chr19:48915728
|
T | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+2164T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915728 | ||||||
chr19:48915761
|
G | A | 195 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0042others(192): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.757+2197G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915761 | ||||||
chr19:48915804
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.757+2240C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915804 | ||||||
chr19:48915807
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.757+2243C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915807 | ||||||
chr19:48915810
|
G | A | 3 | a0001c0001t0001g0341a0001c0001t0010g0184a0001c0001t0016g0340 | 3 | HG02257.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.757+2246G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915810 | ||||||
chr19:48916010
|
A | G | 165 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0109others(162): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.757+2446A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916010 | ||||||
chr19:48916051
|
A | G | 1 | a0001c0001t0008g0178 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.757+2487A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916051 | ||||||
chr19:48916171
|
C | CGT | 40 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0033others(37): Show | 41 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.758-2528_758-2527d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | CGTGT | 13 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0379others(10): Show | 13 | HG01261.hp1 HG02145.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.758-2530_758-2527d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0004g0322 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.758-2536_758-2527d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | CGTGTGTG others(5): Show |
2 | a0001c0001t0001g0016a0001c0001t0004g0329 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.758-2538_758-2527d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | CGTGTGTG others(7): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG01346.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.758-2540_758-2527d others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | CGTGTGTG others(9): Show |
5 | a0001c0001t0001g0104a0001c0001t0006g0082a0001c0001t0006g0084others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-2542_758-2527d others(18): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | CGTGTGTG others(11): Show |
7 | a0002c0004t0001g0032a0002c0004t0001g0040a0002c0004t0001g0041others(4): Show | 7 | HG02486.hp1 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.758-2544_758-2527d others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | CGTGTGTG others(13): Show |
1 | a0001c0001t0013g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.758-2546_758-2527d others(22): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916171
|
C | T | 10 | a0001c0001t0003g0078a0001c0001t0003g0173a0001c0001t0003g0214others(7): Show | 10 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.758-2555C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916171 | ||||||
chr19:48916171
|
CGT | C | 12 | a0001c0001t0001g0328a0001c0001t0001g0330a0001c0001t0001g0385others(9): Show | 13 | HG01516.hp2 HG01517.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.758-2528_758-2527d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | |||||
chr19:48916356
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.758-2370G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916356 | ||||||
chr19:48916383
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.758-2343C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916383 | ||||||
chr19:48916393
|
G | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0114others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-2333G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916393 | ||||||
chr19:48916439
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.758-2287A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916439 | ||||||
chr19:48916583
|
GC | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0033others(29): Show | 33 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.758-2140delC | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916583 | |||||
chr19:48916646
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 136 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.758-2080A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916646 | ||||||
chr19:48916654
|
A | C | 190 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0042others(187): Show | 191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.758-2072A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916654 | ||||||
chr19:48916658
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.758-2068C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916658 | ||||||
chr19:48916676
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 149 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.758-2050C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916676 | ||||||
chr19:48916848
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.758-1878G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916848 | ||||||
chr19:48916977
|
T | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(222): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.758-1749T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916977 | ||||||
chr19:48917056
|
T | C | 376 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(373): Show | 383 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(380): Show |
intron_variant | MODIFIER | c.758-1670T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917056 | ||||||
chr19:48917407
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0386 | 2 | NA18747.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.758-1319C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917407 | ||||||
chr19:48917498
|
A | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0104a0001c0001t0001g0121others(10): Show | 13 | HG01261.hp1 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.758-1228A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917498 | ||||||
chr19:48917498
|
AT | A | 176 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0043others(173): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.758-1218delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917498 | |||||
chr19:48917684
|
C | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0114others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-1042C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917684 | ||||||
chr19:48917696
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0008g0178 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.758-1030A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917696 | ||||||
chr19:48917748
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.758-978G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917748 | ||||||
chr19:48917786
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.758-940G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917786 | ||||||
chr19:48917797
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(220): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.758-929A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917797 | ||||||
chr19:48917798
|
A | T | 1 | a0001c0001t0001g0012 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.758-928A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917798 | ||||||
chr19:48917806
|
C | CT | 23 | a0001c0001t0001g0118a0001c0001t0001g0293a0001c0001t0001g0341others(20): Show | 23 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.758-904dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917806 | |||||
chr19:48917806
|
C | CTT | 10 | a0001c0001t0001g0016a0001c0001t0001g0104a0001c0001t0001g0121others(7): Show | 10 | HG01261.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.758-905_758-904dup others(2): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917806 | |||||
chr19:48917825
|
A | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0114others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-901A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917825 | ||||||
chr19:48917834
|
G | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0114others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-892G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917834 | ||||||
chr19:48917879
|
A | ATGATC | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 148 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.758-845_758-841dup others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917879 | |||||
chr19:48917894
|
C | T | 1 | a0001c0001t0009g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.758-832C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917894 | ||||||
chr19:48917935
|
T | A | 1 | a0004c0009t0001g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-791T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917935 | ||||||
chr19:48917995
|
G | C | 2 | a0001c0001t0001g0311a0001c0001t0001g0327 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.758-731G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917995 | ||||||
chr19:48918101
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.758-625C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918101 | ||||||
chr19:48918379
|
G | A | 1 | a0001c0001t0001g0377 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.758-347G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918379 | ||||||
chr19:48918471
|
A | T | 176 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0043others(173): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.758-255A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918471 | ||||||
chr19:48918495
|
G | C | 1 | a0001c0001t0002g0256 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.758-231G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918495 | ||||||
chr19:48918572
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(232): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.758-154A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918572 | ||||||
chr19:48918646
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 136 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.758-80A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918646 | ||||||
chr19:48918709
|
T | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(219): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.758-17T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918709 | ||||||
chr19:48918814
|
G | A | 1 | a0004c0009t0001g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.816+30G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | chr19 | 48918814 | ||||||
chr19:48918815
|
A | G | 1 | a0004c0009t0001g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.816+31A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | chr19 | 48918815 | ||||||
chr19:48918914
|
CA | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(44): Show | 48 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.817-111delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr19 | 48918914 | |||||
chr19:48918961
|
G | C | 12 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0001g0118others(9): Show | 12 | HG01243.hp2 HG01433.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.817-69G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | chr19 | 48918961 | ||||||
chr19:48919180
|
A | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0033others(29): Show | 33 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.910-14A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 9/12 | chr19 | 48919180 | ||||||
chr19:48919305
|
C | T | 1 | a0001c0001t0002g0353 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1002+19C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919305 | ||||||
chr19:48919395
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0033others(28): Show | 32 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1002+109C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919395 | ||||||
chr19:48919452
|
C | CTTAT | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1002+204_1002+207d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | |||||
chr19:48919452
|
C | CTTATTTA others(1): Show |
5 | a0001c0001t0001g0125a0001c0001t0001g0150a0001c0001t0001g0360others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+200_1002+207d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | |||||
chr19:48919452
|
C | CTTATTTA others(5): Show |
1 | a0001c0001t0002g0152 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1002+196_1002+207d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | |||||
chr19:48919452
|
CTTATTTA others(5): Show |
C | 1 | a0001c0001t0002g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1002+196_1002+207d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | |||||
chr19:48919492
|
T | C | 1 | a0001c0001t0002g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1002+206T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919492 | ||||||
chr19:48919514
|
A | G | 365 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(362): Show | 372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.1002+228A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919514 | ||||||
chr19:48919607
|
A | G | 3 | a0001c0001t0004g0158a0001c0001t0004g0334a0001c0008t0012g0020 | 3 | HG02809.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1002+321A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919607 | ||||||
chr19:48919608
|
G | T | 3 | a0001c0001t0004g0158a0001c0001t0004g0334a0001c0008t0012g0020 | 3 | HG02809.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1002+322G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919608 | ||||||
chr19:48919761
|
A | AT | 17 | a0001c0001t0001g0119a0001c0001t0004g0322a0001c0001t0004g0329others(14): Show | 17 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1002+498dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919761 | |||||
chr19:48919781
|
TTTTC | T | 12 | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0230others(9): Show | 12 | HG01070.hp1 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1002+497_1002+500d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919781 | |||||
chr19:48919782
|
TTTC | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1002+498_1002+500d others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919782 | |||||
chr19:48919783
|
TTC | T | 155 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0030others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1002+499_1002+500d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919783 | |||||
chr19:48919784
|
TC | T | 22 | a0001c0001t0001g0063a0001c0001t0001g0104a0001c0001t0001g0121others(19): Show | 22 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1002+499delC | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919784 | ||||||
chr19:48919785
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0001g0320others(2): Show | 5 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+499C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919785 | ||||||
chr19:48919810
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+524G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919810 | ||||||
chr19:48919814
|
G | T | 37 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0058others(34): Show | 37 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1002+528G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919814 | ||||||
chr19:48919838
|
G | A | 9 | a0001c0001t0001g0043a0001c0003t0001g0001a0001c0003t0001g0018others(6): Show | 10 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002+552G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919838 | ||||||
chr19:48919871
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0104a0001c0001t0013g0112 | 3 | HG02965.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1002+585C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919871 | ||||||
chr19:48919875
|
C | T | 36 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0058others(33): Show | 36 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+589C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919875 | ||||||
chr19:48919900
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1002+614C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919900 | ||||||
chr19:48920058
|
C | T | 26 | a0001c0001t0001g0021a0001c0001t0001g0058a0001c0001t0001g0113others(23): Show | 26 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1002+772C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920058 | ||||||
chr19:48920107
|
G | GC | 378 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(375): Show | 385 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.1002+822dupC | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48920107 | |||||
chr19:48920119
|
G | A | 2 | a0001c0001t0001g0347a0004c0009t0001g0349 | 2 | HG02132.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1002+833G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920119 | ||||||
chr19:48920168
|
C | T | 1 | a0001c0001t0004g0329 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1002+882C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920168 | ||||||
chr19:48920270
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0120a0001c0003t0001g0111others(2): Show | 5 | HG02145.hp2 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-884A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920270 | ||||||
chr19:48920378
|
G | C | 3 | a0001c0001t0006g0082a0001c0001t0006g0084a0001c0001t0006g0122 | 3 | HG02055.hp2 HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1003-776G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920378 | ||||||
chr19:48920448
|
T | G | 19 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0047others(16): Show | 19 | HG00733.hp2 HG01261.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1003-706T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920448 | ||||||
chr19:48920506
|
TTTTA | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0104a0001c0001t0013g0112 | 3 | HG02965.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1003-632_1003-629d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48920506 | |||||
chr19:48920526
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1003-628G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920526 | ||||||
chr19:48920529
|
T | G | 1 | a0004c0009t0001g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1003-625T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920529 | ||||||
chr19:48920530
|
G | T | 1 | a0004c0009t0001g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1003-624G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920530 | ||||||
chr19:48920599
|
T | C | 377 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(374): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1003-555T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920599 | ||||||
chr19:48920704
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0053 | 2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1003-450G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920704 | ||||||
chr19:48920782
|
G | A | 361 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(358): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1003-372G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920782 | ||||||
chr19:48920877
|
C | T | 361 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(358): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1003-277C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920877 | ||||||
chr19:48920960
|
G | A | 359 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(356): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1003-194G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920960 | ||||||
chr19:48920978
|
G | A | 10 | a0001c0001t0004g0322a0001c0001t0004g0329a0001c0001t0016g0340others(7): Show | 10 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-176G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920978 | ||||||
chr19:48920990
|
C | T | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1003-164C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920990 | ||||||
chr19:48921009
|
A | C | 1 | a0001c0001t0003g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1003-145A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921009 | ||||||
chr19:48921054
|
C | A | 10 | a0001c0001t0004g0322a0001c0001t0004g0329a0001c0001t0016g0340others(7): Show | 10 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-100C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921054 | ||||||
chr19:48921097
|
C | T | 154 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1003-57C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921097 | ||||||
chr19:48921124
|
C | A | 154 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1003-30C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921124 | ||||||
chr19:48921382
|
C | T | 11 | a0001c0003t0001g0001a0001c0003t0001g0018a0001c0003t0001g0019others(8): Show | 12 | HG00733.hp2 HG01433.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173+58C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/12 | chr19 | 48921382 | ||||||
chr19:48921455
|
C | T | 1 | a0001c0001t0004g0322 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1173+131C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/12 | chr19 | 48921455 | ||||||
chr19:48921668
|
C | T | 154 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1174-159C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/12 | chr19 | 48921668 | ||||||
chr19:48922001
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0001g0121a0006c0012t0001g0339 | 3 | HG01261.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1279+69G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922001 | ||||||
chr19:48922007
|
G | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0121a0006c0012t0001g0339 | 3 | HG01261.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1279+75G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922007 | ||||||
chr19:48922080
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1279+148G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922080 | ||||||
chr19:48922084
|
T | C | 180 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0058others(177): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1279+152T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922084 | ||||||
chr19:48922085
|
C | T | 3 | a0001c0001t0004g0322a0001c0001t0004g0329a0001c0001t0016g0340 | 3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1279+153C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922085 | ||||||
chr19:48922134
|
G | A | 2 | a0001c0001t0009g0046a0001c0001t0009g0332 | 2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1280-184G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922134 | ||||||
chr19:48922134
|
GGAGGAGG others(23): Show |
G | 3 | a0001c0001t0004g0322a0001c0001t0004g0329a0001c0001t0016g0340 | 3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-169_1280-140d others(32): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 48922134 | |||||
chr19:48922146
|
GGGACCCC others(29): Show |
G | 10 | a0001c0001t0004g0028a0001c0001t0004g0158a0001c0001t0004g0333others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1280-154_1280-119d others(38): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 48922146 | |||||
chr19:48922280
|
G | A | 3 | a0001c0001t0004g0322a0001c0001t0004g0329a0001c0001t0016g0340 | 3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-38G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922280 | ||||||
chr19:48922289
|
G | A | 3 | a0001c0001t0004g0322a0001c0001t0004g0329a0001c0001t0016g0340 | 3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-29G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922289 |