geneid | 4925 |
---|---|
ensemblid | ENSG00000070081.18 |
hgncid | 8044 |
symbol | NUCB2 |
name | nucleobindin 2 |
refseq_nuc | NM_005013.4 |
refseq_prot | NP_005004.1 |
ensembl_nuc | ENST00000529010.6 |
ensembl_prot | ENSP00000436455.1 |
mane_status | MANE Select |
chr | chr11 |
start | 17276739 |
end | 17332211 |
strand | + |
ver | v1.2 |
region | chr11:17276739-17332211 |
region5000 | chr11:17271739-17337211 |
regionname0 | NUCB2_chr11_17276739_17332211 |
regionname5000 | NUCB2_chr11_17271739_17337211 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 420 | 165 | 62 | 40 | 39 | 4 | 18 | 35 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002 | 0/0 | 419 | 100 | 8 | 13 | 71 | 2 | 6 | 54 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0003 | 0/0 | 420 | 92 | 0 | 19 | 59 | 2 | 12 | 44 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0004 | 0/0 | 420 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0005 | 0/0 | 420 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1263 | 164 | 62 | 39 | 39 | 4 | 18 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0002 | 0/0 | 1260 | 95 | 4 | 13 | 70 | 2 | 6 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0003 | 0/0 | 1263 | 91 | 0 | 19 | 58 | 2 | 12 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0004 | 0/0 | 1260 | 4 | 4 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0005 | 0/0 | 1263 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0006 | 0/0 | 1263 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0007 | 0/0 | 1263 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0008 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
c0009 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1038 | 222 | 34 | 37 | 125 | 2 | 23 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
t0002 | 1/0 | 1038 | 128 | 35 | 30 | 43 | 6 | 13 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
t0003 | 0/0 | 1038 | 6 | 0 | 4 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
t0004 | 0/0 | 1038 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
t0005 | 0/0 | 1038 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
t0006 | 0/0 | 1038 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
t0007 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0349 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1263 | 164 | 62 | 39 | 39 | 4 | 18 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0001c0009 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0002 | 0/0 | 1260 | 95 | 4 | 13 | 70 | 2 | 6 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0004 | 0/0 | 1260 | 4 | 4 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0008 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0003c0003 | 0/0 | 1263 | 91 | 0 | 19 | 58 | 2 | 12 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0003c0006 | 0/0 | 1263 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0004c0005 | 0/0 | 1263 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0005c0007 | 0/0 | 1263 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2300 | 69 | 30 | 20 | 11 | 0 | 7 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0001c0001t0002 | 1/0 | 2300 | 92 | 31 | 17 | 28 | 4 | 11 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0001c0001t0004 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0001c0001t0006 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0001c0001t0007 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0001c0009t0002 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0002t0001 | 0/0 | 2297 | 62 | 2 | 1 | 55 | 0 | 4 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0002t0002 | 0/0 | 2297 | 33 | 2 | 12 | 15 | 2 | 2 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0004t0001 | 0/0 | 2297 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0004t0002 | 0/0 | 2297 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0002c0008t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0003c0003t0001 | 0/0 | 2300 | 84 | 0 | 14 | 56 | 2 | 12 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0003c0003t0003 | 0/0 | 2300 | 6 | 0 | 4 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0003c0003t0005 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0003c0006t0001 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0004c0005t0001 | 0/0 | 2300 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
a0005c0007t0001 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | copy fasta | chr11 | 17271739 | 17337211 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0349 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0001c0009t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0004t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0002c0008t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0003t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0003c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0004c0005t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0004c0005t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
a0005c0007t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0001 | g0102 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00140 | hp1 | a0003 | c0003 | t0001 | g0086 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0034 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00423 | hp2 | a0003 | c0003 | t0001 | g0056 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0038 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0055 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0109 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00642 | hp1 | a0003 | c0003 | t0003 | g0031 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00735 | hp2 | a0001 | c0009 | t0002 | g0215 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0169 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0144 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01069 | hp1 | a0004 | c0005 | t0001 | g0333 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01071 | hp1 | a0004 | c0005 | t0001 | g0334 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0053 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0077 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0210 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0337 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01192 | hp2 | a0003 | c0003 | t0001 | g0052 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0198 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0158 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01261 | hp1 | a0003 | c0003 | t0001 | g0342 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0146 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01361 | hp2 | a0003 | c0003 | t0001 | g0088 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0196 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0159 | EUR | IBS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0192 | EUR | IBS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0104 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01943 | hp1 | a0003 | c0003 | t0005 | g0121 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0070 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01975 | hp2 | a0003 | c0003 | t0001 | g0328 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01978 | hp2 | a0003 | c0003 | t0003 | g0319 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01993 | hp1 | a0003 | c0003 | t0003 | g0294 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01993 | hp2 | a0003 | c0003 | t0001 | g0064 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0338 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02040 | hp1 | a0003 | c0003 | t0001 | g0329 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02040 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0036 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02080 | hp1 | a0003 | c0003 | t0003 | g0099 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0054 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02132 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0326 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0336 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0145 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02257 | hp1 | a0002 | c0004 | t0001 | g0312 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02273 | hp1 | a0003 | c0003 | t0003 | g0044 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0045 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02572 | hp2 | a0002 | c0004 | t0002 | g0176 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0085 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02818 | hp1 | a0002 | c0004 | t0002 | g0225 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0068 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03098 | hp1 | a0002 | c0004 | t0001 | g0311 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03239 | hp1 | a0003 | c0003 | t0001 | g0095 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0224 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0087 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0069 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0075 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0072 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0081 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0267 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG03942 | hp2 | a0003 | c0003 | t0001 | g0065 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0033 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0115 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0143 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0346 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18939 | hp1 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18940 | hp2 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18948 | hp1 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0355 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18956 | hp2 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18960 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18963 | hp2 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18965 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18967 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18973 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18983 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18984 | hp2 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18987 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18988 | hp1 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18991 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18993 | hp1 | a0003 | c0006 | t0001 | g0091 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18997 | hp1 | a0005 | c0007 | t0001 | g0043 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18998 | hp1 | a0002 | c0008 | t0001 | g0292 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0059 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19012 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19056 | hp1 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19058 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19059 | hp1 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19059 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19067 | hp2 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19078 | hp2 | a0003 | c0003 | t0001 | g0116 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19080 | hp2 | a0003 | c0003 | t0001 | g0108 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19084 | hp1 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0114 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19086 | hp1 | a0003 | c0003 | t0001 | g0094 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19087 | hp1 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0048 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ASW | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | TSI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0197 | EUR | TSI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0076 | SAS | GIH | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | GIH | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01123 | hp1 | a0003 | c0003 | t0001 | g0035 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18955 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0170 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0349 | REF | REF | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0202 | REF | REF | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17310862
|
A | C | 1 | a0004 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.521A>C | p.His174Pro | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/14 | 766/2300 | 521/1263 | 174/420 | chr11 | 17310862 | ||
chr11:17310872
|
T | A | 1 | a0005 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.531T>A | p.Phe177Leu | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/14 | 776/2300 | 531/1263 | 177/420 | chr11 | 17310872 | ||
chr11:17330136
|
C | G | 3 | a0003a0004a0005 | 95 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(92): Show |
missense_variant | MODERATE | c.1012C>G | p.Gln338Glu | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/14 | 1257/2300 | 1012/1263 | 338/420 | chr11 | 17330136 | ||
chr11:17330930
|
TACA | T | 1 | a0002 | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
conservative_inframe_deletion | MODERATE | c.1207_1209delCAA | p.Gln403del | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/14 | 1452/2300 | 1207/1263 | 403/420 | INFO_REALIGN_3_PRIME | chr11 | 17330930 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17295398
|
G | A | 1 | a0003c0006 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.75G>A | p.Val25Val | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 3/14 | 320/2300 | 75/1263 | 25/420 | chr11 | 17295398 | ||
chr11:17310914
|
T | C | 1 | a0002c0008 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.573T>C | p.Tyr191Tyr | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/14 | 818/2300 | 573/1263 | 191/420 | chr11 | 17310914 | ||
chr11:17330174
|
T | C | 1 | a0001c0009 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1050T>C | p.Tyr350Tyr | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/14 | 1295/2300 | 1050/1263 | 350/420 | chr11 | 17330174 | ||
chr11:17330201
|
T | C | 1 | a0002c0004 | 4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.1077T>C | p.Asn359Asn | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/14 | 1322/2300 | 1077/1263 | 359/420 | chr11 | 17330201 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17276768
|
G | A | 1 | a0001c0001t0004 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-216G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/14 | 18556 | chr11 | 17276768 | |||||
chr11:17276818
|
G | C | 9 | a0001c0001t0001a0002c0002t0001a0002c0004t0001others(6): Show | 228 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(225): Show |
5_prime_UTR_variant | MODIFIER | c.-166G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/14 | 18506 | chr11 | 17276818 | |||||
chr11:17331711
|
C | G | 1 | a0001c0001t0007 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 14/14 | 292 | chr11 | 17331711 | |||||
chr11:17331999
|
T | G | 2 | a0003c0003t0003a0003c0003t0005 | 7 | HG00642.hp1 HG01943.hp1 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*580T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 14/14 | 580 | chr11 | 17331999 | |||||
chr11:17332202
|
G | C | 1 | a0001c0001t0006 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 14/14 | 783 | chr11 | 17332202 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17276919
|
G | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-156+91G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17276919 | ||||||
chr11:17276993
|
G | C | 1 | a0001c0001t0002g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-156+165G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17276993 | ||||||
chr11:17277109
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(210): Show | 216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-156+281C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277109 | ||||||
chr11:17277131
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-156+303C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277131 | ||||||
chr11:17277267
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-156+439A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277267 | ||||||
chr11:17277304
|
C | T | 1 | a0001c0001t0001g0356 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-156+476C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277304 | ||||||
chr11:17277312
|
G | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-156+484G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277312 | ||||||
chr11:17277407
|
A | C | 1 | a0002c0002t0002g0223 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-156+579A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277407 | ||||||
chr11:17277407
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-156+579A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277407 | ||||||
chr11:17277708
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-156+880A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277708 | ||||||
chr11:17277843
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-156+1015T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277843 | ||||||
chr11:17278006
|
A | G | 2 | a0002c0002t0001g0004a0002c0002t0001g0355 | 3 | NA18949.hp1 NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-156+1178A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278006 | ||||||
chr11:17278009
|
T | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+1181T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278009 | ||||||
chr11:17278094
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-156+1266A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278094 | ||||||
chr11:17278107
|
G | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-156+1279G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278107 | ||||||
chr11:17278170
|
C | CT | 40 | a0001c0001t0001g0327a0001c0001t0001g0330a0001c0001t0001g0331others(37): Show | 40 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-156+1365dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17278170 | |||||
chr11:17278170
|
CT | C | 102 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0082others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.-156+1365delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17278170 | |||||
chr11:17278196
|
G | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(31): Show | 35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-156+1368G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278196 | ||||||
chr11:17278214
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-156+1386C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278214 | ||||||
chr11:17278215
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-156+1387A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278215 | ||||||
chr11:17278321
|
A | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(211): Show | 217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-156+1493A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278321 | ||||||
chr11:17278422
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-156+1594T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278422 | ||||||
chr11:17278710
|
T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(211): Show | 217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-156+1882T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278710 | ||||||
chr11:17278870
|
G | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(211): Show | 217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-156+2042G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278870 | ||||||
chr11:17278963
|
C | T | 5 | a0003c0003t0001g0089a0003c0003t0001g0090a0003c0003t0001g0092others(2): Show | 5 | NA18941.hp1 NA18955.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+2135C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278963 | ||||||
chr11:17279022
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-156+2194G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279022 | ||||||
chr11:17279140
|
C | T | 33 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(30): Show | 34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-156+2312C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279140 | ||||||
chr11:17279157
|
A | T | 1 | a0003c0003t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-156+2329A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279157 | ||||||
chr11:17279217
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-156+2389C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279217 | ||||||
chr11:17279297
|
T | G | 110 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0258others(107): Show | 112 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-156+2469T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279297 | ||||||
chr11:17279303
|
G | A | 5 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+2475G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279303 | ||||||
chr11:17279371
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-156+2543C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279371 | ||||||
chr11:17279442
|
C | T | 4 | a0002c0002t0002g0211a0002c0002t0002g0212a0002c0002t0002g0213others(1): Show | 4 | NA18990.hp1 NA18998.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156+2614C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279442 | ||||||
chr11:17279634
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-156+2806A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279634 | ||||||
chr11:17279779
|
AT | A | 81 | a0001c0001t0002g0117a0001c0001t0002g0119a0001c0001t0002g0120others(78): Show | 81 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.-156+2975delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | |||||
chr11:17279779
|
ATT | A | 20 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(17): Show | 20 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-156+2974_-156+297 others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | |||||
chr11:17279779
|
ATTT | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156+2973_-156+297 others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | |||||
chr11:17279779
|
ATTTT | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0245a0001c0001t0001g0246others(115): Show | 121 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-156+2972_-156+297 others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | |||||
chr11:17280031
|
G | A | 1 | a0003c0003t0001g0024 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-155-2758G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280031 | ||||||
chr11:17280106
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-155-2683T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280106 | ||||||
chr11:17280115
|
T | A | 1 | a0001c0001t0001g0321 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-155-2674T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280115 | ||||||
chr11:17280133
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-155-2656A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280133 | ||||||
chr11:17280203
|
T | G | 1 | a0002c0002t0001g0316 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-2586T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280203 | ||||||
chr11:17280362
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-2427A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280362 | ||||||
chr11:17280499
|
G | A | 5 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-155-2290G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280499 | ||||||
chr11:17280683
|
A | G | 2 | a0002c0002t0001g0315a0002c0002t0001g0353 | 2 | HG02135.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-155-2106A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280683 | ||||||
chr11:17280752
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-2037C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280752 | ||||||
chr11:17280761
|
C | T | 4 | a0002c0002t0002g0196a0002c0002t0002g0197a0002c0002t0002g0198others(1): Show | 4 | HG01109.hp1 HG01255.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-2028C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280761 | ||||||
chr11:17280911
|
C | T | 1 | a0003c0003t0001g0113 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-155-1878C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280911 | ||||||
chr11:17280946
|
C | T | 1 | a0002c0002t0001g0314 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-155-1843C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280946 | ||||||
chr11:17281002
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-155-1787A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281002 | ||||||
chr11:17281047
|
C | A | 1 | a0002c0002t0001g0316 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-1742C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281047 | ||||||
chr11:17281048
|
A | C | 1 | a0002c0002t0001g0316 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-1741A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281048 | ||||||
chr11:17281140
|
A | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-155-1649A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281140 | ||||||
chr11:17281559
|
T | A | 1 | a0002c0002t0001g0352 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-155-1230T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281559 | ||||||
chr11:17281651
|
AG | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(29): Show | 33 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-155-1137delG | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281651 | ||||||
chr11:17281858
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-931T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281858 | ||||||
chr11:17281868
|
A | T | 3 | a0001c0001t0001g0348a0001c0001t0001g0349a0001c0001t0001g0350 | 3 | HG01433.hp2 HG02735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-155-921A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281868 | ||||||
chr11:17281996
|
G | C | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-793G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281996 | ||||||
chr11:17282210
|
A | G | 1 | a0002c0002t0001g0243 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-155-579A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282210 | ||||||
chr11:17282214
|
CTA | C | 119 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(116): Show | 121 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-155-571_-155-570d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282214 | |||||
chr11:17282216
|
A | ATC | 86 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-155-572_-155-571i others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282216 | |||||
chr11:17282216
|
A | ATCTATC | 12 | a0001c0001t0001g0101a0002c0002t0001g0029a0003c0003t0001g0036others(9): Show | 12 | HG00544.hp2 HG01074.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-155-572_-155-571i others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282216 | |||||
chr11:17282234
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0322 | 3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-155-555A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282234 | ||||||
chr11:17282236
|
C | A | 1 | a0001c0001t0002g0134 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-155-553C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282236 | ||||||
chr11:17282236
|
C | CTA | 21 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130others(18): Show | 21 | HG00741.hp2 HG01109.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.-155-531_-155-530d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | |||||
chr11:17282236
|
C | CTATCTA | 17 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0178others(14): Show | 17 | HG00621.hp1 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-550_-155-549i others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | |||||
chr11:17282236
|
C | CTATCTAT others(3): Show |
1 | a0001c0001t0002g0208 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | |||||
chr11:17282236
|
C | CTATCTAT others(3): Show |
1 | a0002c0002t0002g0122 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | |||||
chr11:17282236
|
CTA | C | 7 | a0001c0001t0001g0356a0001c0001t0002g0195a0002c0002t0001g0028others(4): Show | 7 | HG01168.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-531_-155-530d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | |||||
chr11:17282238
|
A | ATC | 75 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0002g0131others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-155-550_-155-549i others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | |||||
chr11:17282238
|
A | ATCTATCT others(3): Show |
1 | a0002c0004t0002g0225 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | |||||
chr11:17282238
|
A | ATCTATCT others(7): Show |
1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | |||||
chr11:17282238
|
A | ATCTATCT others(15): Show |
1 | a0001c0001t0001g0020 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-155-550_-155-549i others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | |||||
chr11:17282238
|
A | G | 114 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0254others(111): Show | 116 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-155-551A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282238 | ||||||
chr11:17282240
|
A | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(172): Show | 178 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.-155-549A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282240 | ||||||
chr11:17282240
|
A | G | 1 | a0001c0001t0001g0356 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-155-549A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282240 | ||||||
chr11:17282242
|
A | C | 74 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0073others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-155-547A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282242 | ||||||
chr11:17282242
|
A | G | 14 | a0001c0001t0001g0101a0001c0001t0001g0244a0001c0001t0001g0348others(11): Show | 14 | HG00544.hp2 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-155-547A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282242 | ||||||
chr11:17282244
|
A | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(57): Show | 61 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-155-545A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282244 | ||||||
chr11:17282244
|
A | G | 70 | a0001c0001t0001g0061a0001c0001t0001g0073a0002c0002t0001g0022others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-155-545A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282244 | ||||||
chr11:17282246
|
A | ATCTGTC | 13 | a0001c0001t0001g0082a0001c0001t0001g0096a0002c0002t0001g0029others(10): Show | 13 | HG00408.hp2 HG00642.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.-155-542_-155-541i others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282246 | |||||
chr11:17282246
|
A | C | 73 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0073others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-155-543A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282246 | ||||||
chr11:17282246
|
A | G | 1 | a0003c0003t0001g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-155-543A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282246 | ||||||
chr11:17282248
|
A | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(30): Show | 34 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-155-541A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282248 | ||||||
chr11:17282250
|
A | C | 2 | a0001c0001t0001g0020a0001c0001t0007g0224 | 2 | HG02293.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-155-539A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282250 | ||||||
chr11:17282252
|
A | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(29): Show | 33 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-155-537A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282252 | ||||||
chr11:17282254
|
A | T | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-155-535A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282254 | ||||||
chr11:17282254
|
ATATAT | A | 20 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00544.hp1 HG01081.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-155-533_-155-529d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282254 | |||||
chr11:17282256
|
A | ATT | 9 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-532_-155-531i others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | |||||
chr11:17282256
|
A | ATTT | 8 | a0001c0001t0002g0173a0001c0001t0002g0174a0001c0001t0002g0175others(5): Show | 8 | HG02027.hp1 HG02896.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-532_-155-531i others(5): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | |||||
chr11:17282256
|
A | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(29): Show | 33 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-155-533A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282256 | ||||||
chr11:17282256
|
A | T | 4 | a0001c0001t0002g0177a0001c0001t0002g0195a0002c0002t0002g0223others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-533A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282256 | ||||||
chr11:17282256
|
ATATT | A | 8 | a0001c0001t0001g0339a0002c0002t0001g0335a0002c0002t0001g0340others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-531_-155-528d others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | |||||
chr11:17282256
|
ATATTT | A | 65 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0262others(62): Show | 67 | HG00423.hp1 HG00673.hp1 HG01099.hp2 others(64): Show |
intron_variant | MODIFIER | c.-155-531_-155-527d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | |||||
chr11:17282258
|
A | ATT | 16 | a0001c0001t0002g0117a0001c0001t0002g0155a0001c0001t0002g0156others(13): Show | 16 | HG00597.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-155-517_-155-516d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282258 | |||||
chr11:17282258
|
A | T | 32 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(29): Show | 32 | HG00140.hp2 HG00738.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-155-531A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282258 | ||||||
chr11:17282258
|
AT | A | 12 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0348others(9): Show | 12 | HG00544.hp2 HG01074.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-155-516delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282258 | |||||
chr11:17282258
|
ATTTTT | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0322a0002c0002t0001g0248others(6): Show | 10 | HG00408.hp1 HG02135.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-155-520_-155-516d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282258 | |||||
chr11:17282259
|
T | TA | 3 | a0001c0001t0007g0224a0003c0003t0001g0030a0003c0003t0001g0054 | 3 | HG02129.hp1 HG03486.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-155-530_-155-529i others(3): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | ||||||
chr11:17282259
|
T | TCTATATA others(2): Show |
7 | a0001c0001t0001g0012a0001c0001t0002g0005a0001c0001t0002g0226others(4): Show | 7 | HG01074.hp2 HG01175.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-530_-155-529i others(11): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | ||||||
chr11:17282259
|
T | TCTATCTA others(6): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 14 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-155-530_-155-529i others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | ||||||
chr11:17282259
|
T | TCTATCTA others(6): Show |
2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-155-530_-155-529i others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | ||||||
chr11:17282259
|
T | TCTATCTA others(10): Show |
3 | a0001c0001t0001g0019a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02273.hp2 NA18961.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-155-530_-155-529i others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | ||||||
chr11:17282259
|
T | TCTATCTA others(10): Show |
1 | a0001c0001t0002g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-155-530_-155-529i others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | ||||||
chr11:17282260
|
T | A | 31 | a0001c0001t0002g0135a0002c0002t0001g0022a0002c0002t0001g0023others(28): Show | 31 | HG00642.hp1 HG00673.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.-155-529T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282260 | ||||||
chr11:17282261
|
T | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(38): Show | 42 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-155-528T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282261 | ||||||
chr11:17282262
|
T | A | 2 | a0001c0001t0001g0321a0001c0001t0001g0323 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-155-527T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282262 | ||||||
chr11:17282263
|
T | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(32): Show | 36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-155-526T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282263 | ||||||
chr11:17282273
|
T | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(30): Show | 34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-155-516T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282273 | ||||||
chr11:17282419
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-370C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282419 | ||||||
chr11:17282541
|
A | G | 2 | a0003c0003t0001g0078a0003c0003t0001g0079 | 2 | NA18940.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-155-248A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282541 | ||||||
chr11:17282557
|
G | A | 6 | a0003c0003t0001g0055a0003c0003t0001g0056a0003c0003t0001g0057others(3): Show | 6 | HG00423.hp2 HG00621.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-232G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282557 | ||||||
chr11:17282579
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-210G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282579 | ||||||
chr11:17282592
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-155-197G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282592 | ||||||
chr11:17282770
|
T | A | 1 | a0002c0002t0001g0316 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-19T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282770 | ||||||
chr11:17282770
|
T | C | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-155-19T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282770 | ||||||
chr11:17282771
|
A | T | 1 | a0002c0002t0001g0316 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-18A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282771 | ||||||
chr11:17283055
|
T | TG | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0004g0009 | 3 | HG00642.hp2 HG01258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-1+113dupG | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17283055 | |||||
chr11:17283096
|
A | T | 1 | a0002c0002t0001g0252 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-1+153A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283096 | ||||||
chr11:17283207
|
A | C | 1 | a0001c0001t0002g0233 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-1+264A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283207 | ||||||
chr11:17283256
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-1+313A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283256 | ||||||
chr11:17283369
|
T | C | 1 | a0002c0002t0001g0304 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-1+426T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283369 | ||||||
chr11:17283723
|
C | T | 93 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0082others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+780C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283723 | ||||||
chr11:17283747
|
T | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(211): Show | 217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-1+804T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283747 | ||||||
chr11:17283770
|
T | A | 93 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0082others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+827T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283770 | ||||||
chr11:17283830
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+887A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283830 | ||||||
chr11:17284053
|
G | A | 214 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(211): Show | 217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-1+1110G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284053 | ||||||
chr11:17284067
|
C | G | 1 | a0001c0001t0002g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1+1124C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284067 | ||||||
chr11:17284085
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-1+1142A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284085 | ||||||
chr11:17284103
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-1+1160T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284103 | ||||||
chr11:17284284
|
A | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(212): Show | 218 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-1+1341A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284284 | ||||||
chr11:17284307
|
C | T | 33 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(30): Show | 34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1+1364C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284307 | ||||||
chr11:17284451
|
T | A | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+1508T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284451 | ||||||
chr11:17284706
|
A | AGTTTT | 215 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0073others(212): Show | 218 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-1+1764_-1+1768dup others(5): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17284706 | |||||
chr11:17284767
|
C | G | 1 | a0001c0001t0002g0153 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-1+1824C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284767 | ||||||
chr11:17284863
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+1920A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284863 | ||||||
chr11:17284872
|
CTTCCTCA others(690): Show |
C | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+1930_-1+2626del | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284872 | ||||||
chr11:17284911
|
T | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+1968T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284911 | ||||||
chr11:17285014
|
AATAC | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0101others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-1+2096_-1+2099del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285014 | |||||
chr11:17285107
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1+2164G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285107 | ||||||
chr11:17285165
|
T | C | 10 | a0001c0001t0007g0224a0003c0003t0001g0025a0003c0003t0001g0041others(7): Show | 10 | HG00673.hp2 HG02129.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+2222T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285165 | ||||||
chr11:17285166
|
G | A | 9 | a0003c0003t0001g0025a0003c0003t0001g0041a0003c0003t0001g0054others(6): Show | 9 | HG00673.hp2 HG02129.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+2223G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285166 | ||||||
chr11:17285194
|
A | G | 1 | a0003c0003t0001g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-1+2251A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285194 | ||||||
chr11:17285203
|
A | G | 1 | a0002c0002t0001g0314 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-1+2260A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285203 | ||||||
chr11:17285356
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+2413C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285356 | ||||||
chr11:17285450
|
G | A | 6 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0305others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+2507G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285450 | ||||||
chr11:17285502
|
A | G | 1 | a0002c0002t0001g0303 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-1+2559A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285502 | ||||||
chr11:17285508
|
C | T | 1 | a0002c0002t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1+2565C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285508 | ||||||
chr11:17285564
|
G | A | 2 | a0003c0003t0001g0055a0003c0003t0001g0056 | 2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-1+2621G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285564 | ||||||
chr11:17285576
|
C | CA | 37 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 38 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1+2651dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285576 | |||||
chr11:17285577
|
A | T | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2634A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285577 | ||||||
chr11:17285579
|
A | C | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2636A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285579 | ||||||
chr11:17285580
|
A | T | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2637A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285580 | ||||||
chr11:17285586
|
A | T | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2643A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285586 | ||||||
chr11:17285588
|
A | C | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2645A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285588 | ||||||
chr11:17285600
|
T | A | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2657T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285600 | ||||||
chr11:17285605
|
G | A | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2662G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285605 | ||||||
chr11:17285614
|
G | C | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2671G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285614 | ||||||
chr11:17285615
|
G | A | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2672G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285615 | ||||||
chr11:17285619
|
C | T | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2676C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285619 | ||||||
chr11:17285627
|
C | A | 1 | a0003c0003t0001g0089 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-1+2684C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285627 | ||||||
chr11:17285628
|
C | T | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2685C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285628 | ||||||
chr11:17285661
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1+2718G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285661 | ||||||
chr11:17285701
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1+2758G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285701 | ||||||
chr11:17285743
|
C | CA | 19 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0341others(16): Show | 19 | HG00639.hp2 HG00642.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1+2823dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285743 | |||||
chr11:17285743
|
CA | C | 67 | a0001c0001t0001g0019a0001c0001t0001g0278a0001c0001t0001g0295others(64): Show | 68 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.-1+2823delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285743 | |||||
chr11:17285743
|
CAA | C | 6 | a0001c0001t0007g0224a0002c0002t0001g0004a0002c0002t0001g0301others(3): Show | 7 | HG03486.hp1 NA18942.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+2822_-1+2823del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285743 | |||||
chr11:17285829
|
T | C | 2 | a0001c0001t0001g0354a0001c0001t0002g0128 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1+2886T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285829 | ||||||
chr11:17285867
|
C | T | 1 | a0002c0002t0001g0300 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-1+2924C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285867 | ||||||
chr11:17285934
|
T | TAC | 35 | a0001c0001t0001g0255a0001c0001t0001g0263a0001c0001t0001g0264others(32): Show | 35 | HG00597.hp2 HG00735.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-1+3023_-1+3024dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285934
|
T | TACAC | 22 | a0001c0001t0001g0309a0001c0001t0001g0313a0002c0002t0001g0004others(19): Show | 23 | HG00544.hp1 HG02027.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.-1+3021_-1+3024dup others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285934
|
T | TACACAC | 4 | a0002c0002t0001g0286a0002c0002t0001g0287a0002c0002t0001g0288others(1): Show | 4 | HG00423.hp1 NA18963.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+3019_-1+3024dup others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285934
|
T | TACACACA others(1): Show |
31 | a0001c0001t0001g0295a0002c0002t0001g0002a0002c0002t0001g0242others(28): Show | 32 | HG00408.hp1 HG00673.hp1 HG01978.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1+3017_-1+3024dup others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285934
|
T | TACACACA others(3): Show |
1 | a0003c0003t0005g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-1+3015_-1+3024dup others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285934
|
T | TACACACA others(5): Show |
1 | a0002c0002t0001g0261 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-1+3013_-1+3024dup others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285934
|
TAC | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0244a0001c0001t0001g0245others(47): Show | 51 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1+3023_-1+3024del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285934
|
TACAC | T | 8 | a0001c0001t0001g0269a0001c0001t0002g0137a0001c0001t0002g0156others(5): Show | 8 | HG00639.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+3021_-1+3024del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | |||||
chr11:17285964
|
C | T | 3 | a0003c0003t0001g0025a0003c0003t0001g0041a0003c0003t0001g0094 | 3 | HG00673.hp2 NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-1+3021C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285964 | ||||||
chr11:17286095
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1+3152G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286095 | ||||||
chr11:17286141
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+3198T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286141 | ||||||
chr11:17286241
|
T | G | 1 | a0002c0002t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1+3298T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286241 | ||||||
chr11:17286583
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+3640T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286583 | ||||||
chr11:17286602
|
C | T | 2 | a0002c0002t0001g0251a0002c0002t0001g0352 | 2 | NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-1+3659C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286602 | ||||||
chr11:17286726
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.-1+3783T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286726 | ||||||
chr11:17286921
|
A | G | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+3978A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286921 | ||||||
chr11:17287113
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+4170T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287113 | ||||||
chr11:17287172
|
A | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+4229A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287172 | ||||||
chr11:17287174
|
T | A | 1 | a0001c0001t0001g0351 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-1+4231T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287174 | ||||||
chr11:17287193
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+4250G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287193 | ||||||
chr11:17287287
|
T | G | 1 | a0002c0002t0002g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-1+4344T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287287 | ||||||
chr11:17287339
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+4396A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287339 | ||||||
chr11:17287400
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+4457G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287400 | ||||||
chr11:17287422
|
G | T | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1+4479G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287422 | ||||||
chr11:17287490
|
G | T | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+4547G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287490 | ||||||
chr11:17287493
|
A | G | 5 | a0001c0001t0001g0244a0001c0001t0002g0240a0002c0002t0001g0022others(2): Show | 5 | HG00639.hp2 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+4550A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287493 | ||||||
chr11:17287602
|
A | T | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1+4659A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287602 | ||||||
chr11:17287630
|
AC | A | 27 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0306others(24): Show | 27 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1+4689delC | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287630 | |||||
chr11:17287672
|
C | CA | 102 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0245others(99): Show | 105 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-1+4749dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287672 | |||||
chr11:17287672
|
C | CAA | 6 | a0001c0001t0002g0236a0002c0002t0001g0253a0002c0002t0001g0260others(3): Show | 6 | HG00673.hp1 HG00735.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+4748_-1+4749dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287672 | |||||
chr11:17287672
|
CA | C | 13 | a0001c0001t0002g0131a0001c0001t0002g0167a0001c0001t0002g0219others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+4749delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287672 | |||||
chr11:17287698
|
G | T | 1 | a0002c0002t0001g0285 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-1+4755G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287698 | ||||||
chr11:17287768
|
G | A | 1 | a0003c0003t0001g0064 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-1+4825G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287768 | ||||||
chr11:17287807
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+4864T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287807 | ||||||
chr11:17287913
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+4970G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287913 | ||||||
chr11:17287954
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+5011C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287954 | ||||||
chr11:17287966
|
C | T | 1 | a0003c0003t0001g0039 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-1+5023C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287966 | ||||||
chr11:17288165
|
GT | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+5225delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288165 | |||||
chr11:17288190
|
A | C | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1+5247A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288190 | ||||||
chr11:17288273
|
G | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1+5330G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288273 | ||||||
chr11:17288314
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1+5371A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288314 | ||||||
chr11:17288401
|
C | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5458C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288401 | ||||||
chr11:17288546
|
C | CTTTT | 4 | a0002c0002t0001g0002a0002c0002t0001g0242a0002c0002t0001g0320others(1): Show | 5 | NA18956.hp1 NA18983.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+5605_-1+5606ins others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288546 | |||||
chr11:17288549
|
C | T | 5 | a0002c0002t0001g0002a0002c0002t0001g0242a0002c0002t0001g0289others(2): Show | 6 | NA18956.hp1 NA18979.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5606C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288549 | ||||||
chr11:17288552
|
C | CTTCTTTT others(5): Show |
1 | a0001c0001t0001g0264 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-1+5611_-1+5612ins others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTCTTTT others(6): Show |
12 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0001g0266others(9): Show | 12 | HG00735.hp1 HG01243.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5611_-1+5612ins others(13): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTCTTTT others(7): Show |
2 | a0001c0001t0001g0262a0001c0001t0001g0307 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-1+5611_-1+5612ins others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0244a0001c0001t0001g0330a0002c0002t0001g0023others(5): Show | 8 | HG01081.hp1 HG01168.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+5618_-1+5625dup others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTTTTTT others(2): Show |
99 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0258others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-1+5617_-1+5625dup others(9): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTTTTTT others(3): Show |
62 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0278others(59): Show | 63 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-1+5616_-1+5625dup others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTTTTTT others(4): Show |
22 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0021others(19): Show | 23 | HG00423.hp1 HG01070.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-1+5615_-1+5625dup others(11): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTTTTTT others(5): Show |
20 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(17): Show | 21 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.-1+5614_-1+5625dup others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG01255.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-1+5613_-1+5625dup others(13): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | |||||
chr11:17288552
|
C | T | 5 | a0002c0002t0001g0002a0002c0002t0001g0242a0002c0002t0001g0289others(2): Show | 6 | NA18956.hp1 NA18979.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5609C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288552 | ||||||
chr11:17288679
|
C | T | 1 | a0001c0009t0002g0215 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-1+5736C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288679 | ||||||
chr11:17288703
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1+5760C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288703 | ||||||
chr11:17288844
|
C | T | 86 | a0002c0002t0001g0029a0003c0003t0001g0024a0003c0003t0001g0025others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-1+5901C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288844 | ||||||
chr11:17288845
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1+5902G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288845 | ||||||
chr11:17288877
|
GTA | G | 9 | a0002c0002t0002g0209a0003c0003t0001g0037a0003c0003t0001g0041others(6): Show | 9 | HG00642.hp1 HG00673.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5940del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288877 | |||||
chr11:17288880
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-1+5937T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288880 | ||||||
chr11:17288880
|
T | TAC | 6 | a0001c0001t0002g0221a0003c0003t0001g0055a0003c0003t0001g0066others(3): Show | 6 | HG00621.hp2 HG02080.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
T | TACACACA others(1): Show |
3 | a0003c0003t0001g0040a0003c0003t0001g0051a0003c0003t0001g0065 | 3 | HG02132.hp2 HG02155.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
T | TACACACA others(17): Show |
1 | a0001c0001t0002g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
T | TACACACA others(27): Show |
1 | a0001c0001t0001g0277 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATAC | T | 12 | a0001c0001t0002g0233a0003c0003t0001g0024a0003c0003t0001g0026others(9): Show | 12 | HG01261.hp1 HG02056.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5942del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACAC | T | 12 | a0001c0001t0002g0227a0001c0001t0002g0230a0002c0002t0002g0213others(9): Show | 12 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5944del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(1): Show |
T | 12 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0239others(9): Show | 12 | HG01074.hp2 HG01175.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5946del others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(3): Show |
T | 16 | a0001c0001t0001g0324a0001c0001t0002g0219a0001c0001t0002g0238others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5948del others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(5): Show |
T | 10 | a0001c0001t0001g0356a0003c0003t0001g0059a0003c0003t0001g0074others(7): Show | 10 | HG02109.hp2 HG03492.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5950del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(7): Show |
T | 6 | a0001c0001t0001g0323a0003c0003t0001g0050a0003c0003t0001g0060others(3): Show | 6 | HG00639.hp1 HG01884.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5952del others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(9): Show |
T | 3 | a0001c0001t0001g0321a0002c0002t0001g0029a0003c0003t0001g0025 | 3 | HG02083.hp2 HG02257.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-1+5939_-1+5954del others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(11): Show |
T | 2 | a0003c0003t0001g0032a0003c0003t0001g0047 | 2 | HG02129.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-1+5939_-1+5956del others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(13): Show |
T | 1 | a0003c0003t0003g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-1+5939_-1+5958del others(20): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(15): Show |
T | 3 | a0001c0001t0001g0003a0001c0001t0001g0322a0003c0003t0001g0072 | 4 | HG02922.hp2 HG02970.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5960del others(22): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(17): Show |
T | 1 | a0001c0001t0001g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1+5939_-1+5962del others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288880
|
TATACACA others(21): Show |
T | 2 | a0001c0001t0001g0245a0003c0003t0001g0110 | 2 | HG03579.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-1+5939_-1+5966del others(28): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | |||||
chr11:17288882
|
T | C | 27 | a0001c0001t0001g0277a0001c0001t0002g0156a0001c0001t0002g0157others(24): Show | 27 | HG00099.hp1 HG00621.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1+5939T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288882 | ||||||
chr11:17288882
|
T | TAC | 6 | a0001c0001t0002g0117a0001c0001t0002g0165a0001c0001t0002g0186others(3): Show | 6 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+6007_-1+6008dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACAC | 11 | a0001c0001t0001g0001a0001c0001t0001g0073a0001c0001t0002g0120others(8): Show | 12 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+6005_-1+6008dup others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACAC | 8 | a0001c0001t0001g0012a0001c0001t0001g0096a0001c0001t0001g0269others(5): Show | 8 | HG01192.hp1 HG01261.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+6003_-1+6008dup others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(1): Show |
8 | a0001c0001t0001g0343a0001c0001t0002g0119a0001c0001t0002g0134others(5): Show | 8 | HG01123.hp2 HG02004.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+6001_-1+6008dup others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0263a0001c0001t0002g0183 | 2 | HG02895.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-1+5999_-1+6008dup others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(5): Show |
6 | a0001c0001t0001g0020a0001c0001t0001g0339a0001c0001t0002g0118others(3): Show | 6 | HG01255.hp1 HG02293.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5997_-1+6008dup others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(7): Show |
4 | a0001c0001t0002g0147a0001c0001t0002g0175a0002c0002t0002g0122others(1): Show | 4 | HG00597.hp1 HG03688.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+5995_-1+6008dup others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(9): Show |
2 | a0001c0001t0002g0208a0002c0002t0002g0142 | 2 | HG02132.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-1+5993_-1+6008dup others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(11): Show |
1 | a0001c0001t0002g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+5991_-1+6008dup others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(15): Show |
1 | a0001c0001t0002g0180 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-1+5987_-1+6008dup others(22): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(19): Show |
1 | a0001c0001t0002g0182 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-1+5983_-1+6008dup others(26): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(21): Show |
1 | a0002c0002t0002g0141 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-1+5981_-1+6008dup others(28): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(25): Show |
4 | a0001c0001t0002g0133a0001c0001t0002g0173a0001c0001t0002g0179others(1): Show | 4 | HG03453.hp1 NA18948.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5977_-1+6008dup others(32): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(27): Show |
4 | a0001c0001t0001g0101a0001c0001t0002g0011a0001c0001t0002g0188others(1): Show | 4 | HG01928.hp2 HG02559.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5975_-1+6008dup others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(31): Show |
1 | a0001c0001t0002g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-1+5971_-1+6008dup others(38): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(33): Show |
1 | a0002c0002t0002g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1+5969_-1+6008dup others(40): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(35): Show |
3 | a0001c0001t0002g0189a0001c0001t0002g0206a0001c0001t0006g0161 | 3 | HG01433.hp1 HG02055.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-1+5967_-1+6008dup others(42): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(37): Show |
2 | a0001c0001t0002g0178a0002c0002t0002g0220 | 2 | HG00621.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-1+5965_-1+6008dup others(44): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(41): Show |
3 | a0001c0001t0002g0155a0002c0002t0002g0160a0002c0002t0002g0196 | 3 | HG01496.hp2 HG02300.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-1+5961_-1+6008dup others(48): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
T | TACACACA others(43): Show |
1 | a0001c0001t0002g0159 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-1+5959_-1+6008dup others(50): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TAC | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0330a0003c0003t0001g0329 | 3 | HG01168.hp1 HG02040.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-1+6007_-1+6008del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACAC | T | 7 | a0001c0001t0001g0262a0001c0001t0001g0271a0001c0001t0001g0305others(4): Show | 7 | HG02258.hp2 HG02293.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+6005_-1+6008del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACAC | T | 6 | a0001c0001t0001g0266a0001c0001t0001g0309a0001c0001t0001g0331others(3): Show | 6 | HG01099.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+6003_-1+6008del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0255a0002c0002t0001g0279 | 2 | HG02155.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1+5999_-1+6008del others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0002c0002t0001g0290 | 3 | HG02055.hp1 NA18966.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-1+5997_-1+6008del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0272a0001c0001t0001g0275a0001c0001t0001g0307others(1): Show | 4 | HG02602.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+5995_-1+6008del others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0276a0001c0001t0001g0308a0001c0001t0002g0190others(3): Show | 6 | HG02559.hp2 HG02630.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+5993_-1+6008del others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(11): Show |
T | 10 | a0001c0001t0002g0131a0001c0001t0002g0191a0002c0002t0001g0256others(7): Show | 10 | HG00673.hp1 HG01070.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1+5991_-1+6008del others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(13): Show |
T | 1 | a0002c0002t0001g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-1+5989_-1+6008del others(20): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(15): Show |
T | 20 | a0001c0001t0001g0278a0002c0002t0001g0002a0002c0002t0001g0004others(17): Show | 22 | HG00423.hp1 HG01934.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1+5987_-1+6008del others(22): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(17): Show |
T | 21 | a0001c0001t0001g0258a0001c0001t0001g0295a0001c0001t0001g0325others(18): Show | 21 | HG00544.hp1 HG01943.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1+5985_-1+6008del others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288882
|
TACACACA others(19): Show |
T | 4 | a0001c0001t0001g0259a0002c0002t0001g0299a0002c0002t0001g0316others(1): Show | 4 | HG01978.hp2 HG02280.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5983_-1+6008del others(26): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | |||||
chr11:17288884
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+5941C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288884 | ||||||
chr11:17288920
|
CACACACA others(25): Show |
C | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+5979_-1+6010del others(32): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288920 | |||||
chr11:17288924
|
CACACACA others(27): Show |
C | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+5983_-1+6016del others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288924 | |||||
chr11:17288940
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0002g0150 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-1+5999_-1+6010del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288940 | |||||
chr11:17288940
|
CACACACA others(7): Show |
C | 2 | a0001c0001t0002g0130a0001c0001t0007g0224 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-1+5999_-1+6012del others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288940 | |||||
chr11:17288942
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0002g0195a0001c0001t0002g0241 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1+6001_-1+6010del others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288942 | |||||
chr11:17288942
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0002g0008 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-1+6001_-1+6012del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288942 | |||||
chr11:17288944
|
CACACACA others(1): Show |
C | 4 | a0001c0001t0002g0187a0001c0001t0002g0193a0002c0002t0002g0172others(1): Show | 4 | HG00738.hp2 HG02027.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+6003_-1+6010del others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288944 | |||||
chr11:17288944
|
CACACACA others(5): Show |
C | 2 | a0003c0003t0001g0052a0003c0003t0001g0053 | 2 | HG01074.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-1+6003_-1+6014del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288944 | |||||
chr11:17288946
|
C | T | 4 | a0001c0001t0001g0270a0001c0001t0001g0331a0001c0001t0001g0346others(1): Show | 4 | HG01099.hp2 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+6003C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288946 | ||||||
chr11:17288946
|
CACACAT | C | 4 | a0001c0001t0002g0151a0001c0001t0002g0217a0001c0001t0002g0218others(1): Show | 4 | HG00741.hp1 HG01516.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+6005_-1+6010del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288946 | |||||
chr11:17288948
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-1+6005C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288948 | ||||||
chr11:17288948
|
CACATAT | C | 3 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0127 | 3 | HG01243.hp1 HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+6007_-1+6012del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288948 | |||||
chr11:17288950
|
C | CACACACA others(27): Show |
1 | a0002c0002t0002g0171 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | |||||
chr11:17288950
|
C | CACACACA others(9): Show |
1 | a0003c0003t0001g0328 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | |||||
chr11:17288950
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0347 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | |||||
chr11:17288950
|
C | CACACACA others(1): Show |
5 | a0002c0002t0002g0194a0002c0002t0002g0211a0002c0002t0002g0223others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | |||||
chr11:17288950
|
C | T | 89 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-1+6007C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288950 | ||||||
chr11:17288950
|
CATAT | C | 3 | a0001c0001t0001g0061a0001c0001t0002g0010a0001c0001t0002g0123 | 3 | HG01258.hp2 HG02572.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-1+6018_-1+6021del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | |||||
chr11:17288951
|
A | G | 4 | a0001c0001t0001g0321a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+6008A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288951 | ||||||
chr11:17288952
|
T | C | 79 | a0001c0001t0001g0014a0001c0001t0001g0073a0001c0001t0001g0082others(76): Show | 79 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.-1+6009T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288952 | ||||||
chr11:17288954
|
T | C | 27 | a0001c0001t0001g0073a0001c0001t0001g0096a0001c0001t0001g0101others(24): Show | 27 | HG00621.hp1 HG00642.hp2 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1+6011T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288954 | ||||||
chr11:17288955
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 5 | HG02922.hp2 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+6012A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288955 | ||||||
chr11:17288956
|
T | C | 8 | a0001c0001t0001g0244a0001c0001t0001g0339a0001c0001t0002g0129others(5): Show | 8 | HG01516.hp1 HG02602.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+6013T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288956 | ||||||
chr11:17288958
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+6015T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288958 | ||||||
chr11:17288958
|
TA | T | 32 | a0001c0001t0001g0255a0001c0001t0001g0273a0001c0001t0001g0274others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1+6016delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288958 | ||||||
chr11:17288959
|
A | AT | 28 | a0001c0001t0001g0278a0001c0001t0001g0295a0002c0002t0001g0002others(25): Show | 30 | HG00423.hp1 HG01934.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1+6017dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288959 | |||||
chr11:17288959
|
A | ATT | 3 | a0001c0001t0001g0345a0001c0001t0001g0350a0003c0003t0001g0336 | 3 | HG02148.hp1 HG02735.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-1+6017_-1+6018ins others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288959 | |||||
chr11:17288959
|
A | T | 22 | a0001c0001t0001g0270a0001c0001t0001g0330a0001c0001t0001g0346others(19): Show | 22 | HG00408.hp1 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1+6016A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288959 | ||||||
chr11:17288960
|
TA | T | 24 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1+6018delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288960 | ||||||
chr11:17288961
|
A | AT | 14 | a0001c0001t0001g0021a0001c0001t0001g0325a0001c0001t0002g0216others(11): Show | 14 | HG00544.hp1 HG01943.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+6019dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288961 | |||||
chr11:17288961
|
A | ATTT | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0002c0004t0002g0225 | 3 | HG02818.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1+6019_-1+6020ins others(3): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288961 | |||||
chr11:17288961
|
A | T | 177 | a0001c0001t0001g0255a0001c0001t0001g0270a0001c0001t0001g0272others(174): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-1+6018A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288961 | ||||||
chr11:17288962
|
TA | T | 5 | a0001c0001t0002g0159a0001c0001t0002g0231a0002c0002t0001g0022others(2): Show | 5 | HG01516.hp1 HG02922.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+6020delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288962 | ||||||
chr11:17288963
|
A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+6021_-1+6022ins others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288963 | |||||
chr11:17288963
|
A | ATTT | 7 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(4): Show | 9 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+6030_-1+6032dup others(3): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288963 | |||||
chr11:17288963
|
A | T | 318 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(315): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-1+6020A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288963 | ||||||
chr11:17289133
|
T | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+6190T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289133 | ||||||
chr11:17289294
|
A | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-6030A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289294 | ||||||
chr11:17289320
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0343a0001c0001t0001g0345others(2): Show | 5 | NA18943.hp1 NA18973.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-6004C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289320 | ||||||
chr11:17289502
|
G | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0218 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1-5822G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289502 | ||||||
chr11:17289562
|
T | C | 1 | a0001c0001t0002g0241 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1-5762T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289562 | ||||||
chr11:17289615
|
T | A | 1 | a0002c0002t0001g0100 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1-5709T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289615 | ||||||
chr11:17289645
|
A | G | 1 | a0003c0003t0001g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1-5679A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289645 | ||||||
chr11:17290091
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1-5233C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290091 | ||||||
chr11:17290113
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-5211G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290113 | ||||||
chr11:17290264
|
G | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(234): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1-5060G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290264 | ||||||
chr11:17290280
|
A | T | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1-5044A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290280 | ||||||
chr11:17290553
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1-4771A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290553 | ||||||
chr11:17290649
|
T | C | 2 | a0002c0002t0002g0145a0002c0002t0002g0148 | 2 | HG01123.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1-4675T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290649 | ||||||
chr11:17290652
|
C | G | 1 | a0003c0003t0001g0032 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1-4672C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290652 | ||||||
chr11:17290841
|
T | A | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1-4483T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290841 | ||||||
chr11:17290999
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1-4325C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290999 | ||||||
chr11:17291081
|
C | G | 1 | a0003c0003t0001g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1-4243C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291081 | ||||||
chr11:17291229
|
T | A | 1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1-4095T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291229 | ||||||
chr11:17291323
|
G | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-4001G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291323 | ||||||
chr11:17291462
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-3862C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291462 | ||||||
chr11:17291471
|
G | A | 1 | a0002c0002t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1-3853G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291471 | ||||||
chr11:17291545
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0131a0001c0001t0002g0191 | 2 | HG01070.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1-3773_1-3764dupAA others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-3774_1-3764dupAA others(9): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0327a0001c0001t0002g0189a0001c0001t0002g0228others(1): Show | 4 | HG02683.hp2 HG03017.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-3777_1-3764dupAA others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(8): Show |
91 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(88): Show | 93 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1-3778_1-3764dupAA others(13): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(9): Show |
110 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0061others(107): Show | 112 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(10): Show |
83 | a0001c0001t0001g0246a0001c0001t0001g0259a0001c0001t0001g0262others(80): Show | 83 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(11): Show |
26 | a0002c0002t0001g0029a0002c0002t0001g0280a0003c0003t0001g0026others(23): Show | 26 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(12): Show |
11 | a0001c0001t0001g0278a0003c0003t0001g0038a0003c0003t0001g0067others(8): Show | 11 | HG00544.hp2 HG01934.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(17): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(13): Show |
3 | a0003c0003t0001g0064a0003c0003t0001g0097a0003c0003t0001g0110 | 3 | HG01993.hp2 NA18956.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291545
|
C | CAAAAAAA others(14): Show |
2 | a0003c0003t0001g0104a0003c0003t0001g0116 | 2 | HG01928.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | |||||
chr11:17291628
|
C | G | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1-3696C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291628 | ||||||
chr11:17291663
|
C | G | 1 | a0001c0001t0002g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1-3661C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291663 | ||||||
chr11:17291734
|
A | G | 27 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0306others(24): Show | 27 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.1-3590A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291734 | ||||||
chr11:17291893
|
C | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-3431C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291893 | ||||||
chr11:17291974
|
A | G | 86 | a0002c0002t0001g0029a0003c0003t0001g0024a0003c0003t0001g0025others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1-3350A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291974 | ||||||
chr11:17292029
|
T | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-3295T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292029 | ||||||
chr11:17292609
|
C | T | 1 | a0003c0003t0001g0342 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1-2715C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292609 | ||||||
chr11:17292798
|
T | A | 85 | a0001c0001t0001g0255a0001c0001t0001g0258a0001c0001t0001g0259others(82): Show | 87 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1-2526T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292798 | ||||||
chr11:17292820
|
G | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-2504G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292820 | ||||||
chr11:17292979
|
T | C | 1 | a0001c0001t0002g0241 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1-2345T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292979 | ||||||
chr11:17293041
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1-2283G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293041 | ||||||
chr11:17293232
|
C | T | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-2092C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293232 | ||||||
chr11:17293237
|
G | A | 86 | a0002c0002t0001g0029a0003c0003t0001g0024a0003c0003t0001g0025others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1-2087G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293237 | ||||||
chr11:17293253
|
CA | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1-2052delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17293253 | |||||
chr11:17293408
|
G | GA | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-1915dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17293408 | |||||
chr11:17293887
|
G | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1-1437G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293887 | ||||||
chr11:17294078
|
T | C | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1-1246T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294078 | ||||||
chr11:17294194
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-1130A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294194 | ||||||
chr11:17294482
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1-842C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294482 | ||||||
chr11:17294529
|
CA | C | 8 | a0003c0003t0001g0025a0003c0003t0001g0041a0003c0003t0001g0089others(5): Show | 8 | HG00673.hp2 NA18941.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-793delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17294529 | |||||
chr11:17294622
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1-702A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294622 | ||||||
chr11:17294678
|
T | TA | 29 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(26): Show | 30 | HG00099.hp2 HG00544.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1-623dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17294678 | |||||
chr11:17294678
|
TA | T | 117 | a0001c0001t0001g0244a0001c0001t0001g0254a0001c0001t0001g0270others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1-623delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17294678 | |||||
chr11:17294701
|
A | G | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1-623A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294701 | ||||||
chr11:17294823
|
G | A | 2 | a0003c0003t0001g0054a0003c0003t0001g0066 | 2 | HG02129.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1-501G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294823 | ||||||
chr11:17294838
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-486A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294838 | ||||||
chr11:17295143
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1-181G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17295143 | ||||||
chr11:17295201
|
AT | A | 43 | a0001c0001t0001g0061a0001c0001t0001g0101a0001c0001t0001g0277others(40): Show | 43 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1-113delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17295201 | |||||
chr11:17295993
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 24 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.145-111T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 3/13 | chr11 | 17295993 | ||||||
chr11:17296386
|
A | C | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+175A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296386 | ||||||
chr11:17296387
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+176T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296387 | ||||||
chr11:17296389
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+178T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296389 | ||||||
chr11:17296390
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+179T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296390 | ||||||
chr11:17296391
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+180T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296391 | ||||||
chr11:17296392
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+181A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296392 | ||||||
chr11:17296396
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+185A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296396 | ||||||
chr11:17296398
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+187C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296398 | ||||||
chr11:17296399
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+188A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296399 | ||||||
chr11:17296582
|
G | A | 1 | a0001c0001t0002g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.252+371G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296582 | ||||||
chr11:17296601
|
C | T | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0001g0027 | 3 | NA18964.hp1 NA18965.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.252+390C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296601 | ||||||
chr11:17296689
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252+478A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296689 | ||||||
chr11:17296760
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 24 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.252+549G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296760 | ||||||
chr11:17296981
|
A | G | 1 | a0001c0001t0002g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.252+770A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296981 | ||||||
chr11:17297231
|
T | TAAAAAAT others(313): Show |
1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+1036_252+1037i others(322): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17297231 | |||||
chr11:17297242
|
G | A | 1 | a0002c0002t0001g0100 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.252+1031G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297242 | ||||||
chr11:17297642
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.252+1431A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297642 | ||||||
chr11:17297688
|
G | C | 1 | a0001c0009t0002g0215 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.252+1477G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297688 | ||||||
chr11:17297807
|
T | C | 352 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(349): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.252+1596T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297807 | ||||||
chr11:17297807
|
T | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252+1596T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297807 | ||||||
chr11:17297845
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.252+1634A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297845 | ||||||
chr11:17297971
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 24 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.252+1760A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297971 | ||||||
chr11:17298040
|
C | G | 1 | a0002c0002t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.252+1829C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298040 | ||||||
chr11:17298040
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.252+1829C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298040 | ||||||
chr11:17298081
|
CA | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(213): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.252+1891delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17298081 | |||||
chr11:17298081
|
CAA | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0278a0001c0001t0002g0240others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+1890_252+1891d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17298081 | |||||
chr11:17298091
|
A | G | 1 | a0003c0003t0001g0032 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.252+1880A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298091 | ||||||
chr11:17298102
|
A | G | 5 | a0001c0001t0001g0270a0001c0001t0002g0204a0001c0001t0002g0238others(2): Show | 5 | HG00408.hp1 HG01175.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1891A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298102 | ||||||
chr11:17298128
|
G | A | 1 | a0003c0003t0001g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.252+1917G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298128 | ||||||
chr11:17298337
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.252+2126G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298337 | ||||||
chr11:17298487
|
G | A | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252+2276G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298487 | ||||||
chr11:17298785
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.252+2574G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298785 | ||||||
chr11:17299083
|
G | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.253-2661G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299083 | ||||||
chr11:17299250
|
G | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.253-2494G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299250 | ||||||
chr11:17299280
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.253-2464A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299280 | ||||||
chr11:17299820
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.253-1924C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299820 | ||||||
chr11:17299875
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(236): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.253-1869T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299875 | ||||||
chr11:17299902
|
C | CATAAA | 87 | a0001c0001t0007g0224a0002c0002t0001g0029a0003c0003t0001g0024others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.253-1820_253-1816d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17299902 | |||||
chr11:17299902
|
CATAAA | C | 3 | a0001c0001t0001g0255a0002c0002t0002g0136a0002c0002t0002g0146 | 3 | HG01346.hp2 HG02293.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-1820_253-1816d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17299902 | |||||
chr11:17300019
|
G | GT | 8 | a0001c0001t0001g0003a0001c0001t0001g0245a0001c0001t0001g0246others(5): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-1716dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300019 | |||||
chr11:17300180
|
T | G | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.253-1564T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300180 | ||||||
chr11:17300231
|
A | C | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-1513A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300231 | ||||||
chr11:17300451
|
C | T | 1 | a0003c0003t0001g0111 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.253-1293C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300451 | ||||||
chr11:17300520
|
C | T | 2 | a0002c0002t0001g0285a0002c0002t0001g0317 | 2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.253-1224C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300520 | ||||||
chr11:17300650
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.253-1094A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300650 | ||||||
chr11:17300664
|
C | T | 2 | a0001c0001t0001g0244a0003c0003t0001g0338 | 2 | HG02004.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.253-1080C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300664 | ||||||
chr11:17300706
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.253-1038G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300706 | ||||||
chr11:17300749
|
G | A | 5 | a0003c0003t0001g0055a0003c0003t0001g0056a0003c0003t0001g0057others(2): Show | 5 | HG00423.hp2 HG00621.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-995G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300749 | ||||||
chr11:17300849
|
T | C | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.253-895T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300849 | ||||||
chr11:17300862
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.253-882C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300862 | ||||||
chr11:17300918
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.253-826C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300918 | ||||||
chr11:17300967
|
C | CT | 100 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0001t0001g0082others(97): Show | 100 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.253-755dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300967 | |||||
chr11:17300967
|
C | CTT | 7 | a0001c0001t0002g0149a0001c0001t0002g0153a0001c0001t0002g0181others(4): Show | 7 | HG00741.hp1 HG01109.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-756_253-755dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300967 | |||||
chr11:17300967
|
CT | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0245a0001c0001t0001g0246others(6): Show | 9 | HG01975.hp1 HG02273.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-755delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300967 | |||||
chr11:17301248
|
C | T | 1 | a0002c0002t0001g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.253-496C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301248 | ||||||
chr11:17301272
|
C | CT | 55 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0245others(52): Show | 56 | HG00673.hp1 HG00735.hp1 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.253-449dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17301272 | |||||
chr11:17301272
|
CT | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.253-449delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17301272 | |||||
chr11:17301295
|
T | G | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-449T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301295 | ||||||
chr11:17301296
|
G | A | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-448G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301296 | ||||||
chr11:17301297
|
A | G | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-447A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301297 | ||||||
chr11:17301476
|
C | T | 58 | a0001c0001t0001g0278a0002c0002t0001g0002a0002c0002t0001g0004others(55): Show | 60 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.253-268C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301476 | ||||||
chr11:17301579
|
C | G | 1 | a0003c0003t0001g0066 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.253-165C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301579 | ||||||
chr11:17301632
|
A | G | 1 | a0003c0003t0001g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.253-112A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301632 | ||||||
chr11:17301673
|
T | A | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-71T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301673 | ||||||
chr11:17302237
|
C | T | 1 | a0003c0003t0001g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.379+367C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302237 | ||||||
chr11:17302245
|
C | A | 4 | a0003c0003t0001g0068a0003c0003t0001g0085a0003c0003t0001g0086others(1): Show | 4 | HG00140.hp1 HG02273.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+375C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302245 | ||||||
chr11:17302308
|
T | G | 1 | a0002c0002t0002g0144 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.379+438T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302308 | ||||||
chr11:17302384
|
G | A | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.379+514G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302384 | ||||||
chr11:17302385
|
A | G | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.379+515A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302385 | ||||||
chr11:17302738
|
AT | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(228): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.379+885delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17302738 | |||||
chr11:17302765
|
A | G | 1 | a0003c0003t0001g0035 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.379+895A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302765 | ||||||
chr11:17302770
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.379+900C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302770 | ||||||
chr11:17302779
|
G | A | 6 | a0001c0001t0002g0155a0001c0001t0002g0163a0001c0001t0006g0161others(3): Show | 6 | HG01433.hp1 HG02004.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.379+909G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302779 | ||||||
chr11:17302800
|
C | T | 1 | a0002c0002t0002g0209 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.379+930C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302800 | ||||||
chr11:17302835
|
G | A | 1 | a0001c0001t0001g0351 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.379+965G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302835 | ||||||
chr11:17302890
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+1020T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302890 | ||||||
chr11:17302954
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379+1084G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302954 | ||||||
chr11:17303018
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379+1148G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303018 | ||||||
chr11:17303027
|
C | T | 1 | a0002c0002t0001g0326 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.379+1157C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303027 | ||||||
chr11:17303083
|
G | T | 1 | a0001c0001t0002g0219 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.379+1213G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303083 | ||||||
chr11:17303367
|
A | C | 1 | a0003c0003t0001g0038 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.379+1497A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303367 | ||||||
chr11:17303401
|
A | G | 87 | a0001c0001t0007g0224a0002c0002t0001g0029a0003c0003t0001g0024others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.379+1531A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303401 | ||||||
chr11:17303506
|
A | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+1636A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303506 | ||||||
chr11:17303656
|
G | A | 1 | a0003c0003t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.379+1786G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303656 | ||||||
chr11:17303659
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.379+1789T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303659 | ||||||
chr11:17303884
|
C | CA | 37 | a0001c0001t0001g0061a0001c0001t0001g0245a0001c0001t0001g0273others(34): Show | 37 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.379+2032dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17303884 | |||||
chr11:17303952
|
T | A | 1 | a0005c0007t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.379+2082T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303952 | ||||||
chr11:17304225
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+2355C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304225 | ||||||
chr11:17304243
|
A | T | 1 | a0003c0003t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.379+2373A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304243 | ||||||
chr11:17304246
|
A | G | 1 | a0003c0003t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.379+2376A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304246 | ||||||
chr11:17304355
|
C | A | 1 | a0001c0001t0002g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379+2485C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304355 | ||||||
chr11:17304551
|
G | A | 4 | a0002c0002t0002g0143a0002c0002t0002g0144a0002c0002t0002g0166others(1): Show | 4 | HG00741.hp2 HG01099.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+2681G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304551 | ||||||
chr11:17304571
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.379+2701C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304571 | ||||||
chr11:17304642
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0004t0002g0176 | 3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+2772C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304642 | ||||||
chr11:17304715
|
C | T | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+2845C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304715 | ||||||
chr11:17305062
|
G | A | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.379+3192G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305062 | ||||||
chr11:17305091
|
A | T | 32 | a0001c0001t0001g0295a0002c0002t0001g0028a0002c0002t0001g0063others(29): Show | 32 | HG00597.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.379+3221A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305091 | ||||||
chr11:17305282
|
C | T | 1 | a0002c0002t0001g0267 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.379+3412C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305282 | ||||||
chr11:17305513
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0002g0177 | 2 | HG01496.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379+3643G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305513 | ||||||
chr11:17305566
|
T | G | 1 | a0001c0001t0002g0188 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.379+3696T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305566 | ||||||
chr11:17305862
|
A | G | 1 | a0002c0002t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.380-3710A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305862 | ||||||
chr11:17306328
|
T | C | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.380-3244T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306328 | ||||||
chr11:17306352
|
A | G | 71 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0278others(68): Show | 73 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.380-3220A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306352 | ||||||
chr11:17306554
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.380-3018A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306554 | ||||||
chr11:17306682
|
C | T | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.380-2890C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306682 | ||||||
chr11:17306706
|
C | T | 67 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0324others(64): Show | 69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.380-2866C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306706 | ||||||
chr11:17306820
|
G | A | 1 | a0003c0003t0001g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.380-2752G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306820 | ||||||
chr11:17306868
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.380-2704T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306868 | ||||||
chr11:17306895
|
G | T | 1 | a0002c0004t0002g0225 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.380-2677G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306895 | ||||||
chr11:17306911
|
C | CA | 9 | a0001c0001t0001g0015a0001c0001t0001g0245a0001c0001t0001g0246others(6): Show | 9 | HG01978.hp1 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-2646dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17306911 | |||||
chr11:17306911
|
C | CAA | 59 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(56): Show | 61 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.380-2647_380-2646d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17306911 | |||||
chr11:17306927
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(15): Show | 19 | HG00140.hp2 HG01071.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.380-2645G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306927 | ||||||
chr11:17306929
|
A | C | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.380-2643A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306929 | ||||||
chr11:17306970
|
G | A | 67 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0324others(64): Show | 69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.380-2602G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306970 | ||||||
chr11:17307023
|
T | A | 1 | a0001c0001t0002g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.380-2549T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307023 | ||||||
chr11:17307157
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.380-2415G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307157 | ||||||
chr11:17307197
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-2375C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307197 | ||||||
chr11:17307211
|
G | A | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-2361G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307211 | ||||||
chr11:17307237
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-2335C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307237 | ||||||
chr11:17307315
|
G | A | 3 | a0001c0001t0002g0131a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.380-2257G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307315 | ||||||
chr11:17307355
|
T | C | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0002g0123others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-2217T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307355 | ||||||
chr11:17307451
|
T | G | 1 | a0002c0008t0001g0292 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.380-2121T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307451 | ||||||
chr11:17307665
|
A | G | 2 | a0002c0004t0001g0311a0002c0004t0001g0312 | 2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.380-1907A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307665 | ||||||
chr11:17307688
|
C | T | 4 | a0001c0001t0002g0147a0001c0001t0002g0168a0001c0001t0002g0205others(1): Show | 4 | HG02056.hp1 HG03688.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-1884C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307688 | ||||||
chr11:17307831
|
A | G | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.380-1741A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307831 | ||||||
chr11:17308251
|
G | T | 95 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(92): Show | 97 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.380-1321G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308251 | ||||||
chr11:17308512
|
A | G | 1 | a0001c0001t0002g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.380-1060A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308512 | ||||||
chr11:17308562
|
A | G | 91 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(88): Show | 93 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.380-1010A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308562 | ||||||
chr11:17308567
|
T | A | 2 | a0001c0001t0002g0229a0001c0001t0002g0239 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.380-1005T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308567 | ||||||
chr11:17308634
|
A | G | 1 | a0001c0001t0002g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.380-938A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308634 | ||||||
chr11:17309069
|
T | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0140 | 2 | HG02602.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.380-503T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17309069 | ||||||
chr11:17309508
|
G | A | 1 | a0002c0002t0001g0293 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.380-64G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17309508 | ||||||
chr11:17309810
|
TTATTAAT others(5): Show |
T | 11 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+144_483+155del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 17309810 | |||||
chr11:17309813
|
T | G | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.483+138T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309813 | ||||||
chr11:17309851
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.483+176C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309851 | ||||||
chr11:17309879
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.483+204G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309879 | ||||||
chr11:17309895
|
C | G | 1 | a0003c0003t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.483+220C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309895 | ||||||
chr11:17309928
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.483+253T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309928 | ||||||
chr11:17309952
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.483+277T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309952 | ||||||
chr11:17309989
|
A | C | 1 | a0003c0003t0001g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.483+314A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309989 | ||||||
chr11:17310236
|
CT | C | 96 | a0001c0001t0001g0013a0001c0001t0002g0120a0001c0001t0002g0184others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.483+573delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 17310236 | |||||
chr11:17310261
|
A | G | 18 | a0003c0003t0001g0064a0003c0003t0001g0097a0003c0003t0001g0098others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.484-564A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310261 | ||||||
chr11:17310493
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.484-332C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310493 | ||||||
chr11:17310644
|
C | CAA | 96 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(93): Show | 98 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.484-173_484-172dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 17310644 | |||||
chr11:17310741
|
G | A | 1 | a0001c0001t0001g0306 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.484-84G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310741 | ||||||
chr11:17310796
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.484-29T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310796 | ||||||
chr11:17311038
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.669+28T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/13 | chr11 | 17311038 | ||||||
chr11:17311067
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.669+57C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/13 | chr11 | 17311067 | ||||||
chr11:17311636
|
G | A | 94 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.761-236G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 8/13 | chr11 | 17311636 | ||||||
chr11:17311651
|
A | G | 31 | a0002c0002t0001g0028a0002c0002t0001g0063a0002c0002t0002g0136others(28): Show | 31 | HG00597.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.761-221A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 8/13 | chr11 | 17311651 | ||||||
chr11:17311830
|
T | G | 98 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.761-42T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 8/13 | chr11 | 17311830 | ||||||
chr11:17312229
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0001g0356 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.912+109C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312229 | ||||||
chr11:17312344
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.912+224T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312344 | ||||||
chr11:17312372
|
G | A | 1 | a0002c0002t0001g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+252G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312372 | ||||||
chr11:17312373
|
A | C | 1 | a0002c0002t0001g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+253A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312373 | ||||||
chr11:17312405
|
AT | A | 98 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.912+301delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 17312405 | |||||
chr11:17312466
|
C | T | 8 | a0001c0001t0001g0082a0001c0001t0001g0096a0001c0001t0002g0117others(5): Show | 8 | HG01175.hp2 HG03710.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.912+346C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312466 | ||||||
chr11:17312467
|
G | A | 1 | a0002c0002t0001g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.912+347G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312467 | ||||||
chr11:17312511
|
CTCTGCCT others(12): Show |
C | 1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+393_912+411del others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 17312511 | |||||
chr11:17312695
|
A | G | 98 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.912+575A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312695 | ||||||
chr11:17312781
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.912+661G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312781 | ||||||
chr11:17312799
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.912+679C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312799 | ||||||
chr11:17312863
|
C | G | 1 | a0002c0002t0001g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+743C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312863 | ||||||
chr11:17312864
|
G | C | 1 | a0002c0002t0001g0251 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+744G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312864 | ||||||
chr11:17312893
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+773_912+774ins others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312893 | ||||||
chr11:17312894
|
A | T | 1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+774A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312894 | ||||||
chr11:17313012
|
A | AT | 98 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.912+897dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 17313012 | |||||
chr11:17313018
|
A | T | 115 | a0001c0001t0001g0244a0001c0001t0001g0254a0001c0001t0001g0270others(112): Show | 117 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.912+898A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313018 | ||||||
chr11:17313049
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.912+929C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313049 | ||||||
chr11:17313075
|
T | C | 1 | a0002c0002t0001g0297 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.912+955T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313075 | ||||||
chr11:17313106
|
T | G | 1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+986T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313106 | ||||||
chr11:17313146
|
T | C | 1 | a0003c0003t0001g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.912+1026T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313146 | ||||||
chr11:17313153
|
T | C | 1 | a0002c0002t0001g0287 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.912+1033T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313153 | ||||||
chr11:17313233
|
A | C | 25 | a0001c0001t0001g0255a0001c0001t0001g0258a0001c0001t0001g0259others(22): Show | 25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.912+1113A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313233 | ||||||
chr11:17313444
|
C | T | 1 | a0002c0004t0001g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.912+1324C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313444 | ||||||
chr11:17313469
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.912+1349G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313469 | ||||||
chr11:17313657
|
C | G | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.912+1537C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313657 | ||||||
chr11:17313832
|
G | A | 1 | a0002c0002t0001g0286 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.913-1554G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313832 | ||||||
chr11:17313849
|
G | T | 1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.913-1537G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313849 | ||||||
chr11:17313868
|
T | C | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.913-1518T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313868 | ||||||
chr11:17313919
|
A | T | 1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.913-1467A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313919 | ||||||
chr11:17314278
|
C | A | 1 | a0001c0001t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.913-1108C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314278 | ||||||
chr11:17314370
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.913-1016G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314370 | ||||||
chr11:17314515
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-871A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314515 | ||||||
chr11:17314598
|
A | G | 15 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0327others(12): Show | 15 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.913-788A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314598 | ||||||
chr11:17314599
|
T | A | 1 | a0002c0002t0001g0303 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.913-787T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314599 | ||||||
chr11:17314784
|
G | A | 98 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.913-602G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314784 | ||||||
chr11:17314796
|
T | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.913-590T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314796 | ||||||
chr11:17314864
|
C | T | 94 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0028others(91): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.913-522C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314864 | ||||||
chr11:17315228
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-158C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17315228 | ||||||
chr11:17315288
|
A | G | 2 | a0003c0003t0001g0103a0003c0003t0001g0108 | 2 | NA19080.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.913-98A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17315288 | ||||||
chr11:17315480
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02300.hp2 | splice_region_variant&intron_variant | LOW | c.1002+5T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315480 | ||||||
chr11:17315683
|
T | C | 97 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(94): Show | 99 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1002+208T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315683 | ||||||
chr11:17315732
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+257C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315732 | ||||||
chr11:17315788
|
T | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0269a0001c0001t0001g0321others(14): Show | 18 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1002+313T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315788 | ||||||
chr11:17315849
|
G | T | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1002+374G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315849 | ||||||
chr11:17315866
|
A | G | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1002+391A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315866 | ||||||
chr11:17315874
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1002+399T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315874 | ||||||
chr11:17315897
|
ATG | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1002+424_1002+425d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17315897 | |||||
chr11:17316004
|
G | A | 2 | a0002c0004t0001g0311a0002c0004t0001g0312 | 2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1002+529G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316004 | ||||||
chr11:17316035
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1002+560C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316035 | ||||||
chr11:17316077
|
A | G | 1 | a0003c0003t0001g0097 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1002+602A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316077 | ||||||
chr11:17316132
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+657C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316132 | ||||||
chr11:17316140
|
T | G | 1 | a0001c0001t0002g0126 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1002+665T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316140 | ||||||
chr11:17316172
|
A | G | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+697A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316172 | ||||||
chr11:17316383
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1002+908T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316383 | ||||||
chr11:17316387
|
C | T | 2 | a0002c0002t0001g0283a0002c0002t0001g0310 | 2 | HG00544.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1002+912C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316387 | ||||||
chr11:17316520
|
A | G | 8 | a0003c0003t0001g0062a0003c0003t0001g0067a0003c0003t0001g0071others(5): Show | 8 | HG00597.hp2 NA18940.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1002+1045A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316520 | ||||||
chr11:17316829
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+1354T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316829 | ||||||
chr11:17317021
|
T | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0218 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1002+1546T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317021 | ||||||
chr11:17317045
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0017 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1002+1570T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317045 | ||||||
chr11:17317068
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1002+1593G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317068 | ||||||
chr11:17317139
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1002+1664A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317139 | ||||||
chr11:17317147
|
A | C | 1 | a0002c0002t0001g0281 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1002+1672A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317147 | ||||||
chr11:17317185
|
G | A | 2 | a0001c0001t0002g0232a0001c0001t0002g0237 | 2 | NA18946.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1002+1710G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317185 | ||||||
chr11:17317232
|
T | C | 1 | a0003c0003t0001g0066 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1002+1757T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317232 | ||||||
chr11:17317332
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+1857A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317332 | ||||||
chr11:17317401
|
G | A | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+1926G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317401 | ||||||
chr11:17317459
|
A | G | 1 | a0002c0002t0001g0286 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1002+1984A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317459 | ||||||
chr11:17317504
|
G | A | 1 | a0003c0003t0001g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1002+2029G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317504 | ||||||
chr11:17317514
|
C | T | 1 | a0002c0002t0001g0004 | 2 | NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1002+2039C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317514 | ||||||
chr11:17317520
|
A | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1002+2045A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317520 | ||||||
chr11:17317580
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(262): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1002+2105T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317580 | ||||||
chr11:17317700
|
A | G | 1 | a0003c0003t0001g0111 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002+2225A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317700 | ||||||
chr11:17317718
|
T | C | 1 | a0003c0003t0001g0070 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1002+2243T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317718 | ||||||
chr11:17317764
|
C | T | 2 | a0003c0003t0001g0078a0003c0003t0001g0079 | 2 | NA18940.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1002+2289C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317764 | ||||||
chr11:17317815
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1002+2340T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317815 | ||||||
chr11:17317872
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1002+2397C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317872 | ||||||
chr11:17317946
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0002g0129 | 2 | HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1002+2471T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317946 | ||||||
chr11:17317973
|
G | GT | 14 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0327others(11): Show | 14 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1002+2498_1002+249 others(5): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317973 | ||||||
chr11:17317974
|
C | CT | 100 | a0001c0001t0001g0271a0001c0001t0001g0295a0001c0001t0001g0308others(97): Show | 102 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1002+2521dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17317974 | |||||
chr11:17317974
|
C | T | 15 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0327others(12): Show | 15 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1002+2499C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317974 | ||||||
chr11:17317974
|
CT | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0263a0001c0001t0001g0325others(7): Show | 10 | HG01934.hp2 HG02109.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002+2521delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17317974 | |||||
chr11:17318054
|
C | G | 355 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(352): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1002+2579C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17318054 | ||||||
chr11:17318085
|
C | T | 1 | a0002c0002t0001g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1002+2610C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17318085 | ||||||
chr11:17318329
|
T | TA | 97 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(94): Show | 99 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1002+2864dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17318329 | |||||
chr11:17318654
|
T | C | 1 | a0003c0003t0001g0329 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1002+3179T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17318654 | ||||||
chr11:17319021
|
A | T | 3 | a0001c0001t0001g0246a0002c0002t0002g0222a0003c0003t0001g0055 | 3 | HG00621.hp2 HG02027.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1002+3546A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319021 | ||||||
chr11:17319022
|
T | A | 3 | a0001c0001t0002g0130a0002c0002t0001g0296a0002c0002t0001g0298 | 3 | HG02723.hp1 NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1002+3547T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319022 | ||||||
chr11:17319029
|
A | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0152a0001c0001t0002g0174others(2): Show | 5 | HG02109.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+3554A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319029 | ||||||
chr11:17319150
|
G | A | 24 | a0001c0001t0001g0255a0001c0001t0001g0258a0001c0001t0001g0259others(21): Show | 24 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1002+3675G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319150 | ||||||
chr11:17319319
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1002+3844T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319319 | ||||||
chr11:17319655
|
T | C | 3 | a0001c0001t0002g0155a0001c0001t0002g0163a0001c0001t0006g0161 | 3 | HG01433.hp1 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1002+4180T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319655 | ||||||
chr11:17319684
|
A | G | 1 | a0003c0003t0001g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1002+4209A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319684 | ||||||
chr11:17319934
|
A | G | 1 | a0003c0003t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1002+4459A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319934 | ||||||
chr11:17320009
|
A | G | 1 | a0002c0002t0002g0210 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1002+4534A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320009 | ||||||
chr11:17320030
|
T | G | 98 | a0001c0001t0007g0224a0002c0002t0001g0002a0002c0002t0001g0004others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+4555T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320030 | ||||||
chr11:17320059
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1002+4584G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320059 | ||||||
chr11:17320074
|
C | CT | 95 | a0003c0003t0001g0024a0003c0003t0001g0025a0003c0003t0001g0026others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1002+4606dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17320074 | |||||
chr11:17320605
|
C | T | 4 | a0002c0002t0002g0211a0002c0002t0002g0212a0002c0002t0002g0213others(1): Show | 4 | NA18990.hp1 NA18998.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+5130C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320605 | ||||||
chr11:17321050
|
TG | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1002+5577delG | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17321050 | |||||
chr11:17321066
|
C | G | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+5591C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321066 | ||||||
chr11:17321176
|
A | G | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1002+5701A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321176 | ||||||
chr11:17321202
|
A | AT | 117 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(114): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1002+5740dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17321202 | |||||
chr11:17321240
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1002+5765C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321240 | ||||||
chr11:17321362
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1002+5887C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321362 | ||||||
chr11:17321579
|
C | G | 6 | a0001c0001t0001g0255a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+6104C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321579 | ||||||
chr11:17321617
|
G | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+6142G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321617 | ||||||
chr11:17321894
|
T | A | 8 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(5): Show | 8 | HG00408.hp1 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1002+6419T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321894 | ||||||
chr11:17321897
|
C | G | 1 | a0003c0003t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1002+6422C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321897 | ||||||
chr11:17321939
|
T | C | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+6464T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321939 | ||||||
chr11:17321972
|
C | G | 1 | a0001c0001t0001g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1002+6497C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321972 | ||||||
chr11:17322008
|
C | T | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1002+6533C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322008 | ||||||
chr11:17322009
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1002+6534G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322009 | ||||||
chr11:17322395
|
T | G | 1 | a0002c0002t0002g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1002+6920T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322395 | ||||||
chr11:17322473
|
C | T | 1 | a0002c0002t0001g0249 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1002+6998C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322473 | ||||||
chr11:17322733
|
A | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0207 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1002+7258A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322733 | ||||||
chr11:17322762
|
ATC | A | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+7289_1002+729 others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17322762 | |||||
chr11:17322956
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1003-7171G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322956 | ||||||
chr11:17322975
|
T | G | 1 | a0003c0003t0001g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1003-7152T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322975 | ||||||
chr11:17323008
|
A | C | 3 | a0001c0001t0002g0155a0001c0001t0002g0163a0001c0001t0006g0161 | 3 | HG01433.hp1 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1003-7119A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323008 | ||||||
chr11:17323033
|
T | TA | 25 | a0001c0001t0001g0244a0001c0001t0001g0255a0001c0001t0001g0258others(22): Show | 25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1003-7093dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17323033 | |||||
chr11:17323061
|
A | G | 1 | a0003c0003t0001g0084 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1003-7066A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323061 | ||||||
chr11:17323352
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(262): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1003-6775T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323352 | ||||||
chr11:17323366
|
TATATC | T | 5 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003-6756_1003-675 others(9): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17323366 | |||||
chr11:17323469
|
T | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1003-6658T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323469 | ||||||
chr11:17323484
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1003-6643G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323484 | ||||||
chr11:17323584
|
T | G | 3 | a0002c0004t0001g0311a0002c0004t0001g0312a0002c0004t0002g0225 | 3 | HG02257.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1003-6543T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323584 | ||||||
chr11:17323692
|
T | C | 1 | a0003c0003t0001g0039 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1003-6435T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323692 | ||||||
chr11:17323703
|
G | C | 1 | a0002c0002t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-6424G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323703 | ||||||
chr11:17323704
|
C | A | 1 | a0002c0002t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-6423C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323704 | ||||||
chr11:17323705
|
A | T | 1 | a0002c0002t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-6422A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323705 | ||||||
chr11:17323847
|
T | C | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-6280T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323847 | ||||||
chr11:17323908
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1003-6219G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323908 | ||||||
chr11:17324013
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1003-6114C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324013 | ||||||
chr11:17324140
|
T | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1003-5987T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324140 | ||||||
chr11:17324340
|
C | T | 4 | a0001c0001t0002g0137a0001c0001t0002g0151a0001c0001t0002g0156others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-5787C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324340 | ||||||
chr11:17324473
|
G | T | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-5654G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324473 | ||||||
chr11:17324498
|
A | G | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1003-5629A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324498 | ||||||
chr11:17324528
|
G | C | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-5599G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324528 | ||||||
chr11:17324531
|
C | T | 100 | a0001c0001t0002g0240a0001c0001t0007g0224a0002c0002t0001g0002others(97): Show | 102 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1003-5596C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324531 | ||||||
chr11:17324577
|
G | T | 1 | a0002c0002t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1003-5550G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324577 | ||||||
chr11:17324587
|
C | A | 1 | a0002c0002t0001g0304 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1003-5540C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324587 | ||||||
chr11:17324608
|
A | G | 1 | a0003c0003t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1003-5519A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324608 | ||||||
chr11:17324762
|
A | G | 1 | a0003c0003t0001g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1003-5365A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324762 | ||||||
chr11:17324778
|
G | GTTTATTT others(1): Show |
3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG01243.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1003-5348_1003-534 others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324778 | |||||
chr11:17324780
|
C | CTATT | 54 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0101others(51): Show | 54 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1003-5313_1003-531 others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | |||||
chr11:17324780
|
C | CTATTTAT others(1): Show |
23 | a0001c0001t0001g0255a0001c0001t0001g0258a0001c0001t0001g0259others(20): Show | 23 | HG00735.hp1 HG02055.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1003-5317_1003-531 others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | |||||
chr11:17324780
|
C | CTATTTAT others(5): Show |
1 | a0001c0001t0002g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1003-5321_1003-531 others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | |||||
chr11:17324780
|
C | T | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG01243.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1003-5347C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324780 | ||||||
chr11:17324780
|
CTATT | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1003-5313_1003-531 others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | |||||
chr11:17324780
|
CTATTTAT others(5): Show |
C | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-5321_1003-531 others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | |||||
chr11:17324797
|
T | TA | 7 | a0001c0001t0001g0096a0001c0001t0002g0117a0001c0001t0002g0167others(4): Show | 7 | HG01175.hp2 HG03710.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1003-5329dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324797 | |||||
chr11:17324832
|
C | T | 94 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(91): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1003-5295C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324832 | ||||||
chr11:17324863
|
G | A | 4 | a0002c0004t0001g0311a0002c0004t0001g0312a0002c0004t0002g0176others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-5264G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324863 | ||||||
chr11:17324887
|
C | T | 5 | a0002c0002t0001g0100a0002c0002t0001g0257a0002c0002t0001g0285others(2): Show | 5 | NA18940.hp1 NA18942.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-5240C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324887 | ||||||
chr11:17324892
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1003-5235C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324892 | ||||||
chr11:17325264
|
C | A | 1 | a0002c0002t0002g0160 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1003-4863C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325264 | ||||||
chr11:17325444
|
C | T | 2 | a0001c0001t0001g0354a0001c0001t0002g0128 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1003-4683C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325444 | ||||||
chr11:17325514
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0182 | 2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1003-4613C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325514 | ||||||
chr11:17325812
|
C | CT | 25 | a0001c0001t0001g0244a0001c0001t0001g0255a0001c0001t0001g0258others(22): Show | 25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1003-4308dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17325812 | |||||
chr11:17325833
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1003-4294T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325833 | ||||||
chr11:17325908
|
C | T | 94 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(91): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1003-4219C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325908 | ||||||
chr11:17325933
|
G | A | 2 | a0002c0002t0001g0251a0002c0002t0001g0352 | 2 | NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1003-4194G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325933 | ||||||
chr11:17326013
|
T | C | 25 | a0001c0001t0001g0244a0001c0001t0001g0255a0001c0001t0001g0258others(22): Show | 25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1003-4114T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326013 | ||||||
chr11:17326257
|
C | G | 1 | a0002c0002t0002g0209 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1003-3870C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326257 | ||||||
chr11:17326297
|
G | A | 3 | a0002c0004t0001g0311a0002c0004t0001g0312a0002c0004t0002g0225 | 3 | HG02257.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1003-3830G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326297 | ||||||
chr11:17326311
|
G | GT | 152 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1003-3793dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17326311 | |||||
chr11:17326311
|
G | GTT | 23 | a0001c0001t0001g0014a0001c0001t0001g0244a0003c0003t0001g0024others(20): Show | 23 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1003-3794_1003-379 others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17326311 | |||||
chr11:17326417
|
A | T | 2 | a0002c0002t0001g0296a0002c0002t0001g0298 | 2 | NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1003-3710A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326417 | ||||||
chr11:17326421
|
G | A | 1 | a0003c0003t0001g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1003-3706G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326421 | ||||||
chr11:17326566
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(262): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1003-3561A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326566 | ||||||
chr11:17326608
|
C | T | 1 | a0002c0004t0002g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1003-3519C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326608 | ||||||
chr11:17326628
|
A | G | 1 | a0001c0009t0002g0215 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1003-3499A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326628 | ||||||
chr11:17326705
|
C | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0324others(1): Show | 4 | HG02109.hp2 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-3422C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326705 | ||||||
chr11:17326726
|
CAAGAGAA others(17): Show |
C | 1 | a0003c0003t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1003-3399_1003-337 others(28): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17326726 | |||||
chr11:17326729
|
G | C | 92 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0028others(89): Show | 94 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1003-3398G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326729 | ||||||
chr11:17326760
|
T | C | 2 | a0001c0001t0002g0180a0001c0001t0002g0182 | 2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1003-3367T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326760 | ||||||
chr11:17326841
|
C | A | 1 | a0002c0002t0002g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1003-3286C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326841 | ||||||
chr11:17326990
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1003-3137G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326990 | ||||||
chr11:17326998
|
T | A | 1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-3129T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326998 | ||||||
chr11:17327045
|
G | A | 4 | a0002c0004t0001g0311a0002c0004t0001g0312a0002c0004t0002g0176others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-3082G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327045 | ||||||
chr11:17327049
|
A | G | 1 | a0003c0003t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1003-3078A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327049 | ||||||
chr11:17327138
|
G | A | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-2989G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327138 | ||||||
chr11:17327262
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1003-2865C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327262 | ||||||
chr11:17327331
|
G | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1003-2796G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327331 | ||||||
chr11:17327638
|
C | T | 3 | a0001c0001t0002g0131a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1003-2489C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327638 | ||||||
chr11:17327704
|
T | TAAGAGAC others(322): Show |
1 | a0001c0001t0007g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-2412_1003-241 others(333): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17327704 | |||||
chr11:17327729
|
C | T | 2 | a0003c0003t0003g0048a0003c0003t0003g0099 | 2 | HG02080.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1003-2398C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327729 | ||||||
chr11:17327735
|
C | T | 6 | a0001c0001t0001g0255a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-2392C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327735 | ||||||
chr11:17328000
|
G | A | 1 | a0003c0003t0001g0113 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1003-2127G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328000 | ||||||
chr11:17328094
|
C | T | 4 | a0002c0004t0001g0311a0002c0004t0001g0312a0002c0004t0002g0176others(1): Show | 4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-2033C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328094 | ||||||
chr11:17328097
|
G | A | 20 | a0002c0002t0001g0004a0002c0002t0001g0029a0002c0002t0001g0100others(17): Show | 21 | HG00423.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1003-2030G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328097 | ||||||
chr11:17328645
|
G | A | 1 | a0003c0003t0001g0113 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1003-1482G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328645 | ||||||
chr11:17328723
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1003-1404G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328723 | ||||||
chr11:17328828
|
C | A | 6 | a0003c0003t0001g0032a0003c0003t0001g0042a0003c0003t0001g0045others(3): Show | 6 | HG02129.hp2 HG02523.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-1299C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328828 | ||||||
chr11:17328836
|
G | A | 2 | a0001c0001t0002g0229a0001c0001t0002g0239 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1003-1291G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328836 | ||||||
chr11:17328847
|
C | T | 96 | a0001c0001t0002g0164a0003c0003t0001g0024a0003c0003t0001g0025others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1003-1280C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328847 | ||||||
chr11:17328874
|
C | G | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-1253C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328874 | ||||||
chr11:17328877
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1003-1250G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328877 | ||||||
chr11:17328910
|
C | A | 3 | a0001c0001t0002g0131a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1003-1217C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328910 | ||||||
chr11:17329031
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1003-1096C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329031 | ||||||
chr11:17329093
|
A | G | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-1034A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329093 | ||||||
chr11:17329623
|
C | G | 1 | a0001c0001t0001g0341 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1003-504C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329623 | ||||||
chr11:17329656
|
A | G | 115 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0327others(112): Show | 117 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1003-471A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329656 | ||||||
chr11:17329739
|
C | T | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(95): Show | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-388C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329739 | ||||||
chr11:17329828
|
G | C | 1 | a0002c0002t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-299G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329828 | ||||||
chr11:17330326
|
T | TA | 100 | a0001c0001t0002g0240a0001c0001t0007g0224a0002c0002t0001g0002others(97): Show | 102 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1173+34dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 17330326 | |||||
chr11:17330604
|
G | A | 15 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0327others(12): Show | 15 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1174-298G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330604 | ||||||
chr11:17330670
|
T | A | 1 | a0001c0001t0001g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1174-232T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330670 | ||||||
chr11:17330748
|
C | T | 5 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-154C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330748 | ||||||
chr11:17330791
|
A | C | 26 | a0001c0001t0001g0244a0001c0001t0001g0255a0001c0001t0001g0258others(23): Show | 26 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1174-111A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330791 | ||||||
chr11:17330877
|
T | C | 4 | a0002c0002t0002g0141a0002c0002t0002g0142a0002c0002t0002g0162others(1): Show | 4 | HG00597.hp1 HG02071.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-25T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330877 | ||||||
chr11:17331051
|
T | A | 1 | a0002c0002t0001g0249 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1255+68T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/13 | chr11 | 17331051 | ||||||
chr11:17331340
|
T | C | 2 | a0002c0002t0001g0284a0002c0002t0001g0287 | 2 | HG00423.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1256-72T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/13 | chr11 | 17331340 | ||||||
chr11:17331354
|
A | G | 3 | a0001c0001t0002g0159a0001c0001t0002g0165a0001c0001t0002g0206 | 3 | HG01167.hp2 HG01516.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1256-58A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/13 | chr11 | 17331354 |