Item | Value |
---|---|
geneid | 1142 |
ensemblid | ENSG00000147432.7 |
hgncid | 1963 |
symbol | CHRNB3 |
name | cholinergic receptor nicotinic beta 3 subunit |
refseq_nuc | NM_000749.5 |
refseq_prot | NP_000740.1 |
ensembl_nuc | ENST00000289957.3 |
ensembl_prot | ENSP00000289957.2 |
mane_status | MANE Select |
chr | chr8 |
start | 42697366 |
end | 42737407 |
strand | + |
ver | v1.2 |
region | chr8:42697366-42737407 |
region5000 | chr8:42692366-42742407 |
regionname0 | CHRNB3_chr8_42697366_42737407 |
regionname5000 | CHRNB3_chr8_42692366_42742407 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 458 | 272 | 87 | 54 | 91 | 8 | 30 | 59 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0002 | 0/0 | 458 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0003 | 0/0 | 458 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1377 | 266 | 84 | 53 | 91 | 8 | 28 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
c0002 | 0/0 | 1377 | 9 | 9 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
c0003 | 0/0 | 1377 | 3 | 0 | 1 | 0 | 0 | 2 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
c0004 | 0/0 | 1377 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
c0005 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
c0006 | 0/0 | 1377 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 971 | 133 | 60 | 27 | 32 | 2 | 12 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0002 | 0/1 | 971 | 107 | 10 | 19 | 60 | 2 | 15 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0003 | 0/0 | 971 | 12 | 11 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0004 | 0/0 | 971 | 9 | 9 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0005 | 0/0 | 971 | 6 | 0 | 4 | 0 | 1 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0006 | 0/0 | 971 | 6 | 0 | 2 | 0 | 3 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0007 | 0/0 | 971 | 3 | 3 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0008 | 0/0 | 971 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0009 | 0/0 | 971 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0010 | 0/0 | 971 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0011 | 0/0 | 971 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0012 | 1/0 | 971 | 1 | 0 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
t0013 | 0/0 | 971 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1377 | 266 | 84 | 53 | 91 | 8 | 28 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0003 | 0/0 | 1377 | 3 | 0 | 1 | 0 | 0 | 2 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0004 | 0/0 | 1377 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0005 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0002c0002 | 0/0 | 1377 | 9 | 9 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0003c0006 | 0/0 | 1377 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2347 | 129 | 60 | 26 | 31 | 2 | 10 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0002 | 0/1 | 2347 | 107 | 10 | 19 | 60 | 2 | 15 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0003 | 0/0 | 2347 | 11 | 10 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0005 | 0/0 | 2347 | 6 | 0 | 4 | 0 | 1 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0006 | 0/0 | 2347 | 6 | 0 | 2 | 0 | 3 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0007 | 0/0 | 2347 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0008 | 0/0 | 2347 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0009 | 0/0 | 2347 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0010 | 0/0 | 2347 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0011 | 0/0 | 2347 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0012 | 1/0 | 2347 | 1 | 0 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0001t0013 | 0/0 | 2347 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0003t0001 | 0/0 | 2347 | 3 | 0 | 1 | 0 | 0 | 2 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0004t0007 | 0/0 | 2347 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0001c0005t0003 | 0/0 | 2347 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0002c0002t0004 | 0/0 | 2347 | 9 | 9 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
a0003c0006t0001 | 0/0 | 2347 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | copy fasta | chr8 | 42692366 | 42742407 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0006g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0009g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0012g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0001t0013g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0004t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0004t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0001c0005t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0002c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
a0003c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0224 | EUR | GBR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0186 | EUR | FIN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0143 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0249 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0256 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0229 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | IBS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0215 | EUR | IBS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0214 | EUR | IBS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | IBS | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0157 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0231 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0232 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02055 | hp1 | a0002 | c0002 | t0004 | g0122 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CDX | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CDX | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CDX | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02258 | hp1 | a0001 | c0004 | t0007 | g0026 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0248 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02451 | hp2 | a0002 | c0002 | t0004 | g0138 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02622 | hp2 | a0002 | c0002 | t0004 | g0119 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0141 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0250 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02886 | hp2 | a0002 | c0002 | t0004 | g0120 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0124 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02897 | hp1 | a0002 | c0002 | t0004 | g0125 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0238 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0246 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0107 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03486 | hp1 | a0001 | c0005 | t0003 | g0032 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03491 | hp1 | a0001 | c0001 | t0006 | g0243 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03654 | hp2 | a0001 | c0001 | t0013 | g0275 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0142 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | STU | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | YRI | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CHB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18988 | hp2 | a0003 | c0006 | t0001 | g0050 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19030 | hp2 | a0001 | c0004 | t0007 | g0025 | AFR | LWK | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | YRI | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ASW | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA20129 | hp2 | a0002 | c0002 | t0004 | g0121 | AFR | ASW | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | GIH | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | GIH | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | USA | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA20300 | hp1 | a0002 | c0002 | t0004 | g0126 | AFR | USA | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA20300 | hp2 | a0002 | c0002 | t0004 | g0123 | AFR | USA | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0101 | AFR | LWK | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0163 | REF | REF | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0012 | g0041 | REF | REF | CHRNB3_chr8_42692366_42742407 | CHRNB3 | chr8 | 42692366 | 42742407 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42731780
|
C | G | 1 | a0003 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.473C>G | p.Thr158Arg | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/6 | 654/2347 | 473/1377 | 158/458 | chr8 | 42731780 | ||
chr8:42736592
|
A | G | 1 | a0002 | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
missense_variant | MODERATE | c.1351A>G | p.Lys451Glu | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 1532/2347 | 1351/1377 | 451/458 | chr8 | 42736592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42708739
|
C | T | 1 | a0001c0004 | 2 | HG02258.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.75C>T | p.Ile25Ile | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/6 | 256/2347 | 75/1377 | 25/458 | chr8 | 42708739 | ||
chr8:42708811
|
T | C | 1 | a0001c0005 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.147T>C | p.His49His | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/6 | 328/2347 | 147/1377 | 49/458 | chr8 | 42708811 | ||
chr8:42731922
|
C | T | 1 | a0001c0003 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
synonymous_variant | LOW | c.615C>T | p.Asn205Asn | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/6 | 796/2347 | 615/1377 | 205/458 | chr8 | 42731922 | ||
chr8:42732516
|
G | C | 2 | a0001c0003a0001c0004 | 5 | HG01074.hp2 HG02258.hp1 HG02698.hp1 others(2): Show |
synonymous_variant | LOW | c.1209G>C | p.Ser403Ser | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/6 | 1390/2347 | 1209/1377 | 403/458 | chr8 | 42732516 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42697373
|
G | A | 1 | a0001c0001t0008 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-174G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/6 | 174 | chr8 | 42697373 | |||||
chr8:42697387
|
G | C | 2 | a0001c0001t0005a0001c0001t0009 | 7 | HG00280.hp2 HG01261.hp2 HG01928.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-160G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/6 | 160 | chr8 | 42697387 | |||||
chr8:42697490
|
G | A | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(4): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/6 | chr8 | 42697490 | ||||||
chr8:42736695
|
G | A | 1 | a0001c0001t0009 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 77 | chr8 | 42736695 | |||||
chr8:42736893
|
A | T | 1 | a0001c0001t0010 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*275A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 275 | chr8 | 42736893 | |||||
chr8:42736953
|
G | T | 1 | a0001c0001t0013 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 335 | chr8 | 42736953 | |||||
chr8:42736999
|
A | G | 5 | a0001c0001t0003a0001c0001t0007a0001c0004t0007others(2): Show | 24 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*381A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 381 | chr8 | 42736999 | |||||
chr8:42737011
|
G | A | 4 | a0001c0001t0003a0001c0001t0007a0001c0004t0007others(1): Show | 15 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*393G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 393 | chr8 | 42737011 | |||||
chr8:42737105
|
G | C | 1 | a0002c0002t0004 | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*487G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 487 | chr8 | 42737105 | |||||
chr8:42737160
|
T | C | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | 275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*542T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 542 | chr8 | 42737160 | |||||
chr8:42737246
|
A | T | 4 | a0001c0001t0003a0001c0001t0007a0001c0004t0007others(1): Show | 15 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*628A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 628 | chr8 | 42737246 | |||||
chr8:42737379
|
A | G | 1 | a0002c0002t0004 | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*761A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 761 | chr8 | 42737379 | |||||
chr8:42737389
|
A | G | 1 | a0001c0001t0011 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 6/6 | 771 | chr8 | 42737389 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:42697599
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02015.hp1 | splice_donor_variant&intron_variant | HIGH | c.52+1G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42697599 | ||||||
chr8:42697720
|
A | T | 18 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(15): Show | 18 | HG00673.hp1 HG01975.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.52+122A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42697720 | ||||||
chr8:42697765
|
G | T | 119 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(116): Show | 122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.52+167G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42697765 | ||||||
chr8:42697812
|
GT | G | 6 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 7 | HG02717.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+219delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42697812 | |||||
chr8:42697821
|
ATTTGCTG others(3): Show |
A | 6 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 7 | HG02717.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+226_52+235delTG others(8): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42697821 | |||||
chr8:42697870
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.52+272C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42697870 | ||||||
chr8:42697903
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.52+305G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42697903 | ||||||
chr8:42698010
|
T | C | 29 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(26): Show | 29 | HG00673.hp1 HG01192.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.52+412T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42698010 | ||||||
chr8:42698191
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+593G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42698191 | ||||||
chr8:42698482
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+884G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42698482 | ||||||
chr8:42698651
|
C | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.52+1053C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42698651 | ||||||
chr8:42698935
|
C | G | 1 | a0001c0001t0002g0258 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.52+1337C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42698935 | ||||||
chr8:42699144
|
C | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.52+1546C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42699144 | ||||||
chr8:42699302
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.52+1704G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42699302 | ||||||
chr8:42699620
|
C | G | 119 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(116): Show | 122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.52+2022C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42699620 | ||||||
chr8:42699882
|
C | CT | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.52+2303dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42699882 | |||||
chr8:42699882
|
CT | C | 164 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(161): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.52+2303delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42699882 | |||||
chr8:42699947
|
G | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00140.hp1 HG01261.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+2349G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42699947 | ||||||
chr8:42700205
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+2607T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700205 | ||||||
chr8:42700356
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+2758C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700356 | ||||||
chr8:42700462
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | HG00140.hp1 HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.52+2864C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700462 | ||||||
chr8:42700463
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+2865G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700463 | ||||||
chr8:42700615
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.52+3017C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700615 | ||||||
chr8:42700669
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52+3071G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700669 | ||||||
chr8:42700958
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+3360G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700958 | ||||||
chr8:42700969
|
G | A | 1 | a0001c0001t0002g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.52+3371G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700969 | ||||||
chr8:42700995
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.52+3397T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42700995 | ||||||
chr8:42701011
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+3413T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701011 | ||||||
chr8:42701129
|
G | T | 1 | a0002c0002t0004g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.52+3531G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701129 | ||||||
chr8:42701184
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.52+3586C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701184 | ||||||
chr8:42701213
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+3615C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701213 | ||||||
chr8:42701226
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0002g0006a0001c0001t0002g0247a0001c0001t0002g0257others(3): Show | 7 | HG01099.hp1 HG01169.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+3639_52+3647dup others(9): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42701226 | |||||
chr8:42701226
|
C | CAAAAAAA others(3): Show |
94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(91): Show | 96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.52+3638_52+3647dup others(10): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42701226 | |||||
chr8:42701226
|
C | CAAAAAAA others(4): Show |
15 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0149others(12): Show | 15 | HG00544.hp1 HG00673.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.52+3637_52+3647dup others(11): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42701226 | |||||
chr8:42701226
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0146 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.52+3636_52+3647dup others(12): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42701226 | |||||
chr8:42701226
|
CA | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(147): Show | 153 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.52+3647delA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42701226 | |||||
chr8:42701371
|
A | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+3773A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701371 | ||||||
chr8:42701378
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.52+3780T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701378 | ||||||
chr8:42701454
|
C | T | 118 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 121 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.52+3856C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701454 | ||||||
chr8:42701455
|
G | A | 5 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0031others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+3857G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701455 | ||||||
chr8:42701488
|
G | A | 6 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0159others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+3890G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701488 | ||||||
chr8:42701490
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.52+3892C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701490 | ||||||
chr8:42701509
|
A | C | 118 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 121 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.52+3911A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701509 | ||||||
chr8:42701511
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+3913C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701511 | ||||||
chr8:42701693
|
G | T | 1 | a0001c0001t0010g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.52+4095G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701693 | ||||||
chr8:42701874
|
T | C | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+4276T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42701874 | ||||||
chr8:42702171
|
A | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+4573A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702171 | ||||||
chr8:42702173
|
G | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+4575G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702173 | ||||||
chr8:42702488
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.52+4890C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702488 | ||||||
chr8:42702495
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.52+4897C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702495 | ||||||
chr8:42702505
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.52+4907C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702505 | ||||||
chr8:42702514
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+4916A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702514 | ||||||
chr8:42702633
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+5035C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702633 | ||||||
chr8:42702889
|
C | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG00423.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.52+5291C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702889 | ||||||
chr8:42702910
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+5312G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702910 | ||||||
chr8:42702961
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.52+5363G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42702961 | ||||||
chr8:42703134
|
T | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.52+5536T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703134 | ||||||
chr8:42703195
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-5522G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703195 | ||||||
chr8:42703280
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-5437T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703280 | ||||||
chr8:42703382
|
C | T | 4 | a0002c0002t0004g0124a0002c0002t0004g0125a0002c0002t0004g0126others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5335C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703382 | ||||||
chr8:42703397
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.53-5320C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703397 | ||||||
chr8:42703427
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-5290A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703427 | ||||||
chr8:42703429
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-5288A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703429 | ||||||
chr8:42703431
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-5286A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703431 | ||||||
chr8:42703433
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-5284A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703433 | ||||||
chr8:42703435
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0002g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(27): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0002g0164 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(29): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | NA18999.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(31): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0002g0165 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(28): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0002g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(34): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0175 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(13): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(20): Show |
4 | a0001c0001t0002g0150a0001c0001t0002g0172a0001c0001t0002g0173others(1): Show | 4 | HG00673.hp2 HG01496.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(27): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0002g0171 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(29): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(24): Show |
4 | a0001c0001t0002g0159a0001c0001t0002g0168a0001c0001t0002g0169others(1): Show | 4 | HG01070.hp2 HG01258.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(31): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0002g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(33): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0002g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(37): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0002g0252 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(39): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0187 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(14): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0005g0186 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(28): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(23): Show |
8 | a0001c0001t0002g0006a0001c0001t0002g0181a0001c0001t0002g0182others(5): Show | 9 | HG01257.hp2 HG02148.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(30): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(25): Show |
2 | a0001c0001t0002g0151a0001c0001t0002g0180 | 2 | HG04184.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(32): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(27): Show |
2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(34): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(29): Show |
3 | a0001c0001t0002g0007a0001c0001t0002g0176a0001c0001t0002g0177 | 3 | HG02015.hp1 HG02132.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(36): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(13): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(20): Show |
2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG03942.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(27): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(22): Show |
7 | a0001c0001t0002g0148a0001c0001t0002g0161a0001c0001t0002g0202others(4): Show | 7 | HG00621.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(29): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(24): Show |
3 | a0001c0001t0002g0154a0001c0001t0002g0201a0001c0001t0002g0245 | 3 | HG00423.hp2 NA18944.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(31): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(26): Show |
7 | a0001c0001t0002g0004a0001c0001t0002g0196a0001c0001t0002g0197others(4): Show | 8 | HG00438.hp1 HG00735.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(33): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(28): Show |
6 | a0001c0001t0002g0147a0001c0001t0002g0160a0001c0001t0002g0193others(3): Show | 6 | HG02683.hp2 HG03927.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(35): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(30): Show |
2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(37): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(32): Show |
4 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0189others(1): Show | 4 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(39): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(40): Show |
1 | a0001c0001t0002g0188 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(47): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0006g0214a0001c0001t0006g0215 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(22): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0006g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(24): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0002g0213a0001c0001t0002g0258 | 2 | HG00738.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(28): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0002g0212 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(30): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(25): Show |
3 | a0001c0001t0002g0211a0001c0001t0002g0253a0001c0001t0002g0254 | 3 | HG00741.hp1 HG00741.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(32): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0002g0210 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(34): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAA others(33): Show |
2 | a0001c0001t0002g0208a0001c0001t0002g0209 | 2 | HG02165.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(40): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(12): Show |
1 | a0001c0001t0002g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(19): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(14): Show |
1 | a0001c0001t0002g0225 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(21): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(16): Show |
2 | a0001c0001t0002g0223a0001c0001t0006g0224 | 2 | HG00140.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(23): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(18): Show |
2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(25): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(20): Show |
4 | a0001c0001t0002g0146a0001c0001t0002g0220a0001c0001t0002g0221others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(27): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(24): Show |
4 | a0001c0001t0002g0005a0001c0001t0002g0217a0001c0001t0002g0218others(1): Show | 5 | HG00597.hp1 NA18948.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(31): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(26): Show |
1 | a0001c0001t0002g0255 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(33): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAAAT others(28): Show |
1 | a0001c0001t0002g0216 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(35): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAATA others(5): Show |
3 | a0001c0001t0005g0157a0001c0001t0005g0231a0001c0001t0005g0232 | 3 | HG01928.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(12): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAATA others(21): Show |
3 | a0001c0001t0002g0228a0001c0001t0002g0230a0001c0001t0009g0229 | 3 | HG01261.hp2 HG02145.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(28): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAATA others(27): Show |
2 | a0001c0001t0002g0227a0001c0001t0005g0250 | 2 | HG02145.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(34): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAAATA others(29): Show |
1 | a0001c0001t0002g0226 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(36): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAAATAT others(28): Show |
1 | a0001c0001t0002g0237 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.53-5281_53-5280ins others(35): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | AAAATATA others(23): Show |
2 | a0001c0001t0002g0158a0001c0001t0007g0238 | 2 | HG01978.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.53-5281_53-5280ins others(30): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703435 | |||||
chr8:42703435
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-5282A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703435 | ||||||
chr8:42703437
|
T | A | 6 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235others(3): Show | 6 | HG01169.hp1 HG03490.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-5280T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703437 | ||||||
chr8:42703439
|
T | A | 5 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235others(2): Show | 5 | HG01169.hp1 HG03490.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-5278T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703439 | ||||||
chr8:42703440
|
T | A | 120 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(117): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.53-5277T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703440 | ||||||
chr8:42703440
|
TTA | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(131): Show | 136 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.53-5257_53-5256del others(2): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703440 | |||||
chr8:42703440
|
TTATA | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | HG00140.hp1 HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.53-5259_53-5256del others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703440 | |||||
chr8:42703441
|
T | A | 1 | a0001c0001t0002g0257 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.53-5276T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703441 | ||||||
chr8:42703443
|
T | A | 1 | a0001c0001t0006g0243 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.53-5274T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703443 | ||||||
chr8:42703445
|
T | A | 1 | a0001c0001t0006g0243 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.53-5272T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703445 | ||||||
chr8:42703458
|
A | ATATATAT others(23): Show |
1 | a0001c0004t0007g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-5256_53-5255ins others(30): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703458 | |||||
chr8:42703458
|
A | ATATATAT others(15): Show |
1 | a0001c0004t0007g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.53-5256_53-5255ins others(22): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42703458 | |||||
chr8:42703460
|
A | G | 1 | a0001c0003t0001g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-5257A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703460 | ||||||
chr8:42703542
|
T | C | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.53-5175T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703542 | ||||||
chr8:42703606
|
C | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02523.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.53-5111C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703606 | ||||||
chr8:42703628
|
A | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.53-5089A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703628 | ||||||
chr8:42703653
|
G | A | 5 | a0001c0001t0002g0162a0001c0001t0002g0164a0001c0001t0002g0168others(2): Show | 5 | HG00597.hp2 NA18946.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-5064G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703653 | ||||||
chr8:42703690
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-5027T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703690 | ||||||
chr8:42703742
|
T | G | 29 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(26): Show | 29 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.53-4975T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703742 | ||||||
chr8:42703744
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.53-4973T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42703744 | ||||||
chr8:42704013
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-4704C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704013 | ||||||
chr8:42704156
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.53-4561G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704156 | ||||||
chr8:42704241
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-4476T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704241 | ||||||
chr8:42704324
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00140.hp1 HG01261.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-4393T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704324 | ||||||
chr8:42704355
|
A | G | 6 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 7 | HG02717.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-4362A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704355 | ||||||
chr8:42704443
|
G | A | 121 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(118): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.53-4274G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704443 | ||||||
chr8:42704481
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.53-4236C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704481 | ||||||
chr8:42704606
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.53-4111C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704606 | ||||||
chr8:42704654
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.53-4063C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704654 | ||||||
chr8:42704672
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-4045G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704672 | ||||||
chr8:42704673
|
C | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-4044C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704673 | ||||||
chr8:42704698
|
G | GTGTGTGT others(7): Show |
2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-4017_53-4016ins others(14): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42704698 | |||||
chr8:42704699
|
T | C | 1 | a0001c0001t0002g0202 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.53-4018T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704699 | ||||||
chr8:42704749
|
G | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-3968G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704749 | ||||||
chr8:42704751
|
G | A | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.53-3966G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704751 | ||||||
chr8:42704795
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG00544.hp2 HG02165.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.53-3922A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704795 | ||||||
chr8:42704838
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-3879C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704838 | ||||||
chr8:42704894
|
T | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-3823T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704894 | ||||||
chr8:42704911
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.53-3806G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42704911 | ||||||
chr8:42705018
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.53-3699C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705018 | ||||||
chr8:42705106
|
A | G | 120 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(117): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.53-3611A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705106 | ||||||
chr8:42705170
|
A | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-3547A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705170 | ||||||
chr8:42705193
|
A | C | 120 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(117): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.53-3524A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705193 | ||||||
chr8:42705369
|
G | T | 1 | a0001c0001t0003g0033 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-3348G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705369 | ||||||
chr8:42705389
|
C | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(28): Show | 31 | HG00140.hp1 HG00673.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.53-3328C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705389 | ||||||
chr8:42705401
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-3316G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705401 | ||||||
chr8:42705555
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-3162C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705555 | ||||||
chr8:42705574
|
C | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-3143C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705574 | ||||||
chr8:42705746
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.53-2971G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705746 | ||||||
chr8:42705933
|
C | A | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.53-2784C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42705933 | ||||||
chr8:42706495
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.53-2222A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42706495 | ||||||
chr8:42706498
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0002g0247 | 2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.53-2219G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42706498 | ||||||
chr8:42706506
|
G | A | 2 | a0002c0002t0004g0124a0002c0002t0004g0125 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.53-2211G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42706506 | ||||||
chr8:42706719
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.53-1998G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42706719 | ||||||
chr8:42706781
|
G | C | 1 | a0001c0001t0002g0152 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.53-1936G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42706781 | ||||||
chr8:42707072
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-1645T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707072 | ||||||
chr8:42707097
|
G | A | 1 | a0002c0002t0004g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.53-1620G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707097 | ||||||
chr8:42707143
|
C | T | 28 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(25): Show | 28 | HG00673.hp1 HG01192.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.53-1574C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707143 | ||||||
chr8:42707505
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.53-1212G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707505 | ||||||
chr8:42707634
|
G | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-1083G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707634 | ||||||
chr8:42707710
|
A | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-1007A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707710 | ||||||
chr8:42707714
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.53-1003G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707714 | ||||||
chr8:42707795
|
G | A | 119 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(116): Show | 122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.53-922G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707795 | ||||||
chr8:42707819
|
A | G | 12 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(9): Show | 12 | HG01074.hp2 HG02055.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.53-898A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707819 | ||||||
chr8:42707862
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-855T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707862 | ||||||
chr8:42707876
|
G | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0131 | 3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.53-841G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42707876 | ||||||
chr8:42708032
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(268): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.53-685A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708032 | ||||||
chr8:42708060
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.53-657G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708060 | ||||||
chr8:42708066
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-651G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708066 | ||||||
chr8:42708120
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53-597G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708120 | ||||||
chr8:42708136
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.53-581T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708136 | ||||||
chr8:42708189
|
G | A | 9 | a0001c0001t0002g0004a0002c0002t0004g0119a0002c0002t0004g0120others(6): Show | 10 | HG02015.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-528G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708189 | ||||||
chr8:42708192
|
C | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-525C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708192 | ||||||
chr8:42708233
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.53-484G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708233 | ||||||
chr8:42708344
|
T | C | 7 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG02280.hp2 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-373T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708344 | ||||||
chr8:42708414
|
C | T | 119 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(116): Show | 122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.53-303C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708414 | ||||||
chr8:42708421
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-296G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708421 | ||||||
chr8:42708474
|
T | TACAC | 36 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(33): Show | 36 | HG00140.hp1 HG00673.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.53-223_53-220dupCA others(2): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42708474 | |||||
chr8:42708474
|
T | TACACAC | 24 | a0001c0001t0002g0150a0001c0001t0003g0001a0001c0001t0003g0008others(21): Show | 25 | HG00673.hp2 HG01074.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.53-225_53-220dupCA others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42708474 | |||||
chr8:42708474
|
T | TACACACA others(1): Show |
101 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(98): Show | 104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.53-227_53-220dupCA others(6): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42708474 | |||||
chr8:42708474
|
T | TACACACA others(3): Show |
14 | a0001c0001t0002g0148a0001c0001t0002g0152a0001c0001t0002g0153others(11): Show | 14 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.53-229_53-220dupCA others(8): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42708474 | |||||
chr8:42708474
|
T | TACACACA others(5): Show |
2 | a0001c0001t0002g0202a0001c0001t0005g0250 | 2 | HG02735.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.53-231_53-220dupCA others(10): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 42708474 | |||||
chr8:42708498
|
A | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-219A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708498 | ||||||
chr8:42708558
|
G | A | 1 | a0001c0001t0002g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.53-159G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708558 | ||||||
chr8:42708634
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-83C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708634 | ||||||
chr8:42708652
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.53-65T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 1/5 | chr8 | 42708652 | ||||||
chr8:42708939
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+71A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42708939 | ||||||
chr8:42709034
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+166C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709034 | ||||||
chr8:42709081
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.204+213G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709081 | ||||||
chr8:42709089
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+221C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709089 | ||||||
chr8:42709133
|
C | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(8): Show | 12 | HG01243.hp1 HG02615.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.204+265C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709133 | ||||||
chr8:42709241
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+373G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709241 | ||||||
chr8:42709349
|
G | A | 5 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0031others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+481G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709349 | ||||||
chr8:42709356
|
C | T | 6 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 7 | HG02717.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+488C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709356 | ||||||
chr8:42709357
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00140.hp1 HG01261.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+489A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709357 | ||||||
chr8:42709384
|
T | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+516T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709384 | ||||||
chr8:42709385
|
T | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+517T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709385 | ||||||
chr8:42709389
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+521T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709389 | ||||||
chr8:42709391
|
A | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+523A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709391 | ||||||
chr8:42709393
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+525G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709393 | ||||||
chr8:42709400
|
T | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+532T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709400 | ||||||
chr8:42709401
|
T | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+533T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709401 | ||||||
chr8:42709404
|
TAGAAGAA others(8): Show |
T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+538_204+552del others(15): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 42709404 | |||||
chr8:42709420
|
A | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+552A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709420 | ||||||
chr8:42709422
|
T | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+554T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709422 | ||||||
chr8:42709509
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.204+641T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709509 | ||||||
chr8:42709588
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.204+720C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709588 | ||||||
chr8:42709642
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.205-748G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709642 | ||||||
chr8:42709691
|
G | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.205-699G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709691 | ||||||
chr8:42709724
|
C | G | 1 | a0001c0001t0002g0189 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.205-666C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709724 | ||||||
chr8:42709737
|
A | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.205-653A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709737 | ||||||
chr8:42709830
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.205-560C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709830 | ||||||
chr8:42709852
|
G | A | 1 | a0002c0002t0004g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.205-538G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709852 | ||||||
chr8:42709962
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.205-428C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42709962 | ||||||
chr8:42710066
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.205-324G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 2/5 | chr8 | 42710066 | ||||||
chr8:42710495
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.249+61G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710495 | ||||||
chr8:42710500
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+66T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710500 | ||||||
chr8:42710580
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+146T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710580 | ||||||
chr8:42710653
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+219T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710653 | ||||||
chr8:42710702
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249+268G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710702 | ||||||
chr8:42710729
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+295G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710729 | ||||||
chr8:42710874
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.249+440G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710874 | ||||||
chr8:42710896
|
A | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+462A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710896 | ||||||
chr8:42710962
|
C | T | 4 | a0002c0002t0004g0124a0002c0002t0004g0125a0002c0002t0004g0126others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+528C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710962 | ||||||
chr8:42710963
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.249+529G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42710963 | ||||||
chr8:42711022
|
A | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(8): Show | 12 | HG01243.hp1 HG02615.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+588A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711022 | ||||||
chr8:42711359
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(272): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.249+925A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711359 | ||||||
chr8:42711591
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+1157C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711591 | ||||||
chr8:42711705
|
T | C | 1 | a0001c0001t0002g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.249+1271T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711705 | ||||||
chr8:42711706
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.249+1272A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711706 | ||||||
chr8:42711750
|
T | C | 17 | a0001c0001t0002g0190a0001c0001t0002g0192a0001c0001t0002g0211others(14): Show | 17 | HG00558.hp2 HG01074.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.249+1316T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711750 | ||||||
chr8:42711846
|
C | T | 1 | a0001c0001t0002g0195 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.249+1412C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711846 | ||||||
chr8:42711929
|
A | G | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+1495A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711929 | ||||||
chr8:42711935
|
C | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+1501C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711935 | ||||||
chr8:42711945
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+1511C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711945 | ||||||
chr8:42711977
|
T | G | 5 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0031others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+1543T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711977 | ||||||
chr8:42711995
|
C | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+1561C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42711995 | ||||||
chr8:42712016
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+1582C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42712016 | ||||||
chr8:42712165
|
G | A | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+1731G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42712165 | ||||||
chr8:42712814
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.249+2380C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42712814 | ||||||
chr8:42712823
|
C | G | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+2389C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42712823 | ||||||
chr8:42712859
|
C | CT | 114 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0112others(111): Show | 117 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.249+2445dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42712859 | |||||
chr8:42712859
|
C | CTT | 8 | a0001c0001t0002g0200a0001c0001t0002g0204a0001c0001t0002g0237others(5): Show | 8 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+2444_249+2445d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42712859 | |||||
chr8:42712859
|
CT | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0052others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+2445delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42712859 | |||||
chr8:42712901
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0084others(7): Show | 11 | HG01106.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+2467G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42712901 | ||||||
chr8:42713020
|
C | T | 12 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(9): Show | 12 | HG01074.hp2 HG02055.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+2586C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713020 | ||||||
chr8:42713250
|
G | A | 18 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(15): Show | 18 | HG00673.hp1 HG01975.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.249+2816G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713250 | ||||||
chr8:42713280
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249+2846A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713280 | ||||||
chr8:42713294
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.249+2860C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713294 | ||||||
chr8:42713331
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.249+2897G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713331 | ||||||
chr8:42713434
|
C | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249+3000C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713434 | ||||||
chr8:42713625
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+3191G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713625 | ||||||
chr8:42713745
|
G | A | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+3311G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713745 | ||||||
chr8:42713964
|
G | A | 5 | a0001c0001t0002g0162a0001c0001t0002g0164a0001c0001t0002g0168others(2): Show | 5 | HG00597.hp2 NA18946.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+3530G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42713964 | ||||||
chr8:42714047
|
T | G | 1 | a0001c0001t0002g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.249+3613T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714047 | ||||||
chr8:42714070
|
C | T | 16 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0036others(13): Show | 17 | HG01243.hp1 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+3636C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714070 | ||||||
chr8:42714092
|
T | G | 1 | a0001c0001t0006g0243 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.249+3658T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714092 | ||||||
chr8:42714207
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.249+3773G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714207 | ||||||
chr8:42714234
|
G | A | 30 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(27): Show | 30 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.249+3800G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714234 | ||||||
chr8:42714234
|
GCCTGTAA others(4171): Show |
G | 1 | a0001c0001t0001g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.249+3836_249+8013d others(2): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42714234 | |||||
chr8:42714339
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.249+3905A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714339 | ||||||
chr8:42714340
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.249+3906A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714340 | ||||||
chr8:42714433
|
C | T | 12 | a0001c0001t0002g0005a0001c0001t0002g0145a0001c0001t0002g0191others(9): Show | 13 | HG00423.hp2 HG02071.hp2 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+3999C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714433 | ||||||
chr8:42714440
|
G | C | 1 | a0001c0004t0007g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+4006G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714440 | ||||||
chr8:42714483
|
T | TCAAAA | 4 | a0002c0002t0004g0124a0002c0002t0004g0125a0002c0002t0004g0126others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+4076_249+4080d others(7): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42714483 | |||||
chr8:42714483
|
TCAAAACA others(3): Show |
T | 1 | a0001c0001t0001g0110 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.249+4071_249+4080d others(12): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42714483 | |||||
chr8:42714613
|
G | GGT | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+4180_249+4181d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42714613 | |||||
chr8:42714790
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249+4356G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714790 | ||||||
chr8:42714828
|
C | G | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.249+4394C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714828 | ||||||
chr8:42714839
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00140.hp1 HG01261.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+4405G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714839 | ||||||
chr8:42714875
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0086others(3): Show | 7 | HG01106.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+4441A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714875 | ||||||
chr8:42714977
|
A | T | 1 | a0001c0001t0002g0173 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.249+4543A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42714977 | ||||||
chr8:42715272
|
G | C | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+4838G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715272 | ||||||
chr8:42715633
|
C | CCT | 12 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(9): Show | 12 | HG01074.hp2 HG02055.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+5200_249+5201d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42715633 | |||||
chr8:42715735
|
A | G | 7 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(4): Show | 8 | HG02717.hp2 HG02922.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+5301A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715735 | ||||||
chr8:42715797
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5363C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715797 | ||||||
chr8:42715893
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5459T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715893 | ||||||
chr8:42715897
|
G | C | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+5463G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715897 | ||||||
chr8:42715976
|
C | CCT | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+5542_249+5543i others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715976 | ||||||
chr8:42715976
|
C | CCTTT | 8 | a0001c0004t0007g0025a0002c0002t0004g0119a0002c0002t0004g0120others(5): Show | 8 | HG02451.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+5542_249+5543i others(6): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715976 | ||||||
chr8:42715976
|
C | CT | 86 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0136others(83): Show | 88 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.249+5562dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42715976 | |||||
chr8:42715976
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.249+5542C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42715976 | ||||||
chr8:42716032
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5598G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716032 | ||||||
chr8:42716035
|
G | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5601G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716035 | ||||||
chr8:42716085
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5651T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716085 | ||||||
chr8:42716090
|
T | C | 1 | a0001c0001t0002g0198 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.249+5656T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716090 | ||||||
chr8:42716091
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.249+5657T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716091 | ||||||
chr8:42716132
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5698T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716132 | ||||||
chr8:42716133
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5699G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716133 | ||||||
chr8:42716156
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5722C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716156 | ||||||
chr8:42716188
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5754G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716188 | ||||||
chr8:42716238
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5804G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716238 | ||||||
chr8:42716274
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+5840G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716274 | ||||||
chr8:42716285
|
CT | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5857delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42716285 | |||||
chr8:42716360
|
CCAAATTT others(7): Show |
C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+5928_249+5941d others(16): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42716360 | |||||
chr8:42716474
|
A | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6040A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716474 | ||||||
chr8:42716492
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6058A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716492 | ||||||
chr8:42716503
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.249+6069T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716503 | ||||||
chr8:42716512
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6078T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716512 | ||||||
chr8:42716540
|
T | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6106T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716540 | ||||||
chr8:42716553
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.249+6119A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716553 | ||||||
chr8:42716698
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00140.hp1 HG01261.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+6264C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716698 | ||||||
chr8:42716700
|
G | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6266G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716700 | ||||||
chr8:42716728
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6294C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716728 | ||||||
chr8:42716737
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6303A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716737 | ||||||
chr8:42716836
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.249+6402T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716836 | ||||||
chr8:42716955
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6521C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716955 | ||||||
chr8:42716975
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6541G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716975 | ||||||
chr8:42716976
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.249+6542C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42716976 | ||||||
chr8:42717058
|
G | A | 29 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(26): Show | 29 | HG00673.hp1 HG01192.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.249+6624G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717058 | ||||||
chr8:42717087
|
AGACTGGC others(314): Show |
A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+6657_249+6977d others(2): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717087 | |||||
chr8:42717105
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0091a0001c0001t0001g0092 | 3 | HG02280.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.249+6671G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717105 | ||||||
chr8:42717303
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.249+6869G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717303 | ||||||
chr8:42717360
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0084others(7): Show | 11 | HG01106.hp2 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+6926C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717360 | ||||||
chr8:42717373
|
CA | C | 44 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(41): Show | 44 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.249+6971delA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717373 | |||||
chr8:42717373
|
CAA | C | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0088others(3): Show | 6 | HG01169.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+6970_249+6971d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717373 | |||||
chr8:42717373
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0109a0001c0001t0002g0247 | 2 | HG01243.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.249+6960_249+6971d others(14): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717373 | |||||
chr8:42717373
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0002g0168a0001c0001t0002g0181 | 2 | NA18946.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.249+6958_249+6971d others(16): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717373 | |||||
chr8:42717403
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0002g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.249+6971_249+6972i others(39): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(26): Show |
2 | a0001c0001t0002g0146a0001c0001t0002g0209 | 2 | HG02165.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.249+6971_249+6972i others(35): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0002g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.249+6971_249+6972i others(34): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(24): Show |
3 | a0001c0001t0002g0150a0001c0001t0002g0221a0001c0001t0002g0223 | 3 | HG00673.hp2 HG01071.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.249+6971_249+6972i others(33): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(23): Show |
5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0002g0155others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(32): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0002g0222a0001c0001t0002g0241 | 2 | HG01069.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.249+6971_249+6972i others(31): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(21): Show |
6 | a0001c0001t0002g0145a0001c0001t0002g0164a0001c0001t0002g0171others(3): Show | 6 | HG00597.hp2 HG01928.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(30): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(20): Show |
3 | a0001c0001t0002g0149a0001c0001t0002g0179a0001c0001t0002g0225 | 3 | HG01257.hp1 HG01496.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.249+6971_249+6972i others(29): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(19): Show |
8 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0001g0110others(5): Show | 8 | HG00280.hp1 HG00280.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(28): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(18): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0085others(12): Show | 16 | HG00423.hp2 HG00544.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(27): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(17): Show |
19 | a0001c0001t0001g0082a0001c0001t0001g0098a0001c0001t0001g0099others(16): Show | 20 | HG01106.hp1 HG01258.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(26): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(16): Show |
12 | a0001c0001t0001g0134a0001c0001t0002g0151a0001c0001t0002g0153others(9): Show | 12 | HG00558.hp1 HG02735.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(25): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0038a0001c0001t0002g0197 | 2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.249+6971_249+6972i others(24): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0252 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.249+6971_249+6972i others(20): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(10): Show |
5 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0177others(2): Show | 6 | HG02015.hp1 HG02015.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(19): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(9): Show |
4 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02683.hp1 NA18942.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(18): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(8): Show |
4 | a0001c0001t0001g0039a0001c0001t0001g0260a0001c0001t0001g0265others(1): Show | 4 | HG01261.hp1 HG03017.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(17): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0040 | 3 | HG02896.hp2 HG03491.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.249+6971_249+6972i others(16): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(5): Show |
14 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00673.hp1 HG01192.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(14): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(4): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0074others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(13): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0118a0001c0001t0002g0200 | 2 | HG00438.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.249+6971_249+6972i others(12): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAA others(2): Show |
9 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0090others(6): Show | 10 | HG00558.hp2 HG00735.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(11): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAAAAAAG | 6 | a0001c0001t0001g0092a0001c0001t0002g0165a0001c0001t0002g0166others(3): Show | 6 | HG00140.hp2 HG00408.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+6971_249+6972i others(9): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AAG | 7 | a0001c0001t0001g0111a0001c0001t0002g0006a0001c0001t0002g0144others(4): Show | 8 | HG01884.hp1 HG02109.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+6970_249+6971i others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717403 | |||||
chr8:42717403
|
A | AG | 12 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0002g0147others(9): Show | 12 | HG02148.hp1 HG02723.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+6969_249+6970i others(3): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717403 | ||||||
chr8:42717403
|
A | G | 93 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0027others(90): Show | 94 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.249+6969A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717403 | ||||||
chr8:42717408
|
C | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(257): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.249+6974C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717408 | ||||||
chr8:42717446
|
T | C | 6 | a0001c0001t0002g0225a0001c0001t0006g0214a0001c0001t0006g0215others(3): Show | 6 | HG00140.hp2 HG01099.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+7012T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717446 | ||||||
chr8:42717494
|
A | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.249+7060A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717494 | ||||||
chr8:42717503
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0169 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.249+7069T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717503 | ||||||
chr8:42717547
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.249+7113T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717547 | ||||||
chr8:42717552
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7118A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717552 | ||||||
chr8:42717625
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7191C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717625 | ||||||
chr8:42717710
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7276C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717710 | ||||||
chr8:42717811
|
T | C | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+7377T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717811 | ||||||
chr8:42717819
|
C | CT | 43 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0023others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.249+7409dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717819 | |||||
chr8:42717819
|
CT | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00140.hp1 HG01192.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7409delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42717819 | |||||
chr8:42717878
|
T | A | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+7444T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717878 | ||||||
chr8:42717879
|
A | G | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+7445A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717879 | ||||||
chr8:42717894
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7460A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717894 | ||||||
chr8:42717896
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7462A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717896 | ||||||
chr8:42717910
|
A | G | 180 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.249+7476A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717910 | ||||||
chr8:42717926
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7492G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717926 | ||||||
chr8:42717929
|
T | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7495T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717929 | ||||||
chr8:42717948
|
T | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0044others(27): Show | 31 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.249+7514T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42717948 | ||||||
chr8:42718021
|
C | CAG | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7588_249+7589d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42718021 | |||||
chr8:42718021
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG01243.hp2 HG01433.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+7587C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718021 | ||||||
chr8:42718028
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7594G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718028 | ||||||
chr8:42718051
|
G | GA | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7619dupA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42718051 | |||||
chr8:42718105
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7671T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718105 | ||||||
chr8:42718149
|
G | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7715G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718149 | ||||||
chr8:42718213
|
T | G | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+7779T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718213 | ||||||
chr8:42718231
|
T | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7797T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718231 | ||||||
chr8:42718291
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7857G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718291 | ||||||
chr8:42718400
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+7966A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718400 | ||||||
chr8:42718437
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8003G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718437 | ||||||
chr8:42718481
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8047A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718481 | ||||||
chr8:42718483
|
C | T | 1 | a0001c0001t0010g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.249+8049C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718483 | ||||||
chr8:42718487
|
C | G | 1 | a0001c0001t0010g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.249+8053C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718487 | ||||||
chr8:42718493
|
G | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8059G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718493 | ||||||
chr8:42718501
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8067A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718501 | ||||||
chr8:42718542
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8108A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718542 | ||||||
chr8:42718566
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8132G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718566 | ||||||
chr8:42718605
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8171A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718605 | ||||||
chr8:42718622
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8188G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718622 | ||||||
chr8:42718630
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.249+8196G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718630 | ||||||
chr8:42718660
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8226A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718660 | ||||||
chr8:42718672
|
C | CA | 34 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0042others(31): Show | 34 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.249+8266dupA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42718672 | |||||
chr8:42718672
|
CA | C | 43 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.249+8266delA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42718672 | |||||
chr8:42718672
|
CAA | C | 25 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0037others(22): Show | 26 | HG01074.hp2 HG01243.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+8265_249+8266d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42718672 | |||||
chr8:42718672
|
CAAAAAAA | C | 6 | a0001c0001t0002g0154a0001c0001t0002g0158a0001c0001t0002g0183others(3): Show | 6 | HG01261.hp2 HG01978.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+8260_249+8266d others(9): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42718672 | |||||
chr8:42718672
|
CAAAAAAA others(1): Show |
C | 105 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(102): Show | 108 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.249+8259_249+8266d others(10): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42718672 | |||||
chr8:42718680
|
A | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8246A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718680 | ||||||
chr8:42718686
|
A | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8252A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718686 | ||||||
chr8:42718691
|
A | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8257A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718691 | ||||||
chr8:42718719
|
T | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8285T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718719 | ||||||
chr8:42718740
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8306C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718740 | ||||||
chr8:42718745
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8311C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718745 | ||||||
chr8:42718746
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8312A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718746 | ||||||
chr8:42718785
|
T | C | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+8351T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718785 | ||||||
chr8:42718823
|
C | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8389C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718823 | ||||||
chr8:42718834
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.249+8400C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718834 | ||||||
chr8:42718865
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8431G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42718865 | ||||||
chr8:42719007
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8573T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719007 | ||||||
chr8:42719008
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8574C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719008 | ||||||
chr8:42719045
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8611G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719045 | ||||||
chr8:42719057
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.249+8623C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719057 | ||||||
chr8:42719083
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8649T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719083 | ||||||
chr8:42719205
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+8771C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719205 | ||||||
chr8:42719233
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8799C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719233 | ||||||
chr8:42719377
|
G | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8943G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719377 | ||||||
chr8:42719413
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+8979A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719413 | ||||||
chr8:42719449
|
A | G | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+9015A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719449 | ||||||
chr8:42719453
|
C | T | 181 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(178): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.249+9019C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719453 | ||||||
chr8:42719455
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9021A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719455 | ||||||
chr8:42719478
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9044T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719478 | ||||||
chr8:42719508
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9074A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719508 | ||||||
chr8:42719572
|
A | G | 1 | a0001c0001t0003g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249+9138A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719572 | ||||||
chr8:42719605
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9171C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719605 | ||||||
chr8:42719638
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.249+9204C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719638 | ||||||
chr8:42719788
|
G | A | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+9354G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719788 | ||||||
chr8:42719800
|
G | T | 1 | a0001c0001t0002g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.249+9366G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719800 | ||||||
chr8:42719884
|
G | A | 2 | a0001c0001t0002g0154a0001c0001t0002g0237 | 2 | NA18944.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.249+9450G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719884 | ||||||
chr8:42719987
|
C | T | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+9553C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42719987 | ||||||
chr8:42720044
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9610T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720044 | ||||||
chr8:42720048
|
C | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0179 | 2 | NA18961.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.249+9614C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720048 | ||||||
chr8:42720048
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9614C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720048 | ||||||
chr8:42720077
|
T | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9643T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720077 | ||||||
chr8:42720111
|
C | CT | 22 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0042others(19): Show | 22 | HG00423.hp1 HG01071.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.249+9711dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
C | CTT | 21 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0038others(18): Show | 22 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.249+9710_249+9711d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
C | CTTT | 21 | a0001c0001t0001g0024a0001c0001t0001g0056a0001c0001t0001g0062others(18): Show | 21 | HG00544.hp2 HG00738.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+9709_249+9711d others(5): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CT | C | 10 | a0001c0001t0001g0051a0001c0001t0001g0105a0001c0001t0001g0127others(7): Show | 10 | HG00673.hp2 HG01081.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.249+9711delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTT | C | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0118others(7): Show | 12 | HG02155.hp1 HG02155.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+9710_249+9711d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTTT | C | 28 | a0001c0001t0002g0145a0001c0001t0002g0147a0001c0001t0002g0152others(25): Show | 28 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.249+9709_249+9711d others(5): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTTTT | C | 85 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0007others(82): Show | 87 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.249+9708_249+9711d others(6): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0004g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.249+9700_249+9711d others(14): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTTTTTTT others(6): Show |
C | 8 | a0001c0001t0001g0052a0002c0002t0004g0119a0002c0002t0004g0120others(5): Show | 8 | HG02451.hp2 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+9699_249+9711d others(15): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0004t0007g0025others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+9698_249+9711d others(16): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTTTTTTT others(8): Show |
C | 31 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(28): Show | 31 | HG00673.hp1 HG01074.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.249+9697_249+9711d others(17): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720111
|
CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0001g0268a0001c0001t0001g0274a0001c0001t0001g0276 | 3 | HG01975.hp2 HG03710.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.249+9696_249+9711d others(18): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42720111 | |||||
chr8:42720189
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249+9755C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720189 | ||||||
chr8:42720190
|
G | A | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+9756G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720190 | ||||||
chr8:42720192
|
T | G | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+9758T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720192 | ||||||
chr8:42720209
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9775A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720209 | ||||||
chr8:42720218
|
A | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9784A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720218 | ||||||
chr8:42720240
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9806T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720240 | ||||||
chr8:42720244
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9810T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720244 | ||||||
chr8:42720256
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9822C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720256 | ||||||
chr8:42720259
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9825G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720259 | ||||||
chr8:42720262
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9828T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720262 | ||||||
chr8:42720265
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9831G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720265 | ||||||
chr8:42720272
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9838T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720272 | ||||||
chr8:42720304
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0177a0001c0001t0002g0208 | 4 | HG02015.hp2 HG02132.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+9870C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720304 | ||||||
chr8:42720305
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9871G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720305 | ||||||
chr8:42720314
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9880C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720314 | ||||||
chr8:42720360
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9926C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720360 | ||||||
chr8:42720403
|
C | A | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+9969C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720403 | ||||||
chr8:42720403
|
C | G | 5 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(2): Show | 5 | HG01074.hp2 HG02258.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+9969C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720403 | ||||||
chr8:42720422
|
G | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+9988G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720422 | ||||||
chr8:42720522
|
C | T | 1 | a0001c0001t0006g0243 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.250-10072C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720522 | ||||||
chr8:42720540
|
G | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-10054G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720540 | ||||||
chr8:42720557
|
T | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-10037T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720557 | ||||||
chr8:42720582
|
C | A | 1 | a0001c0001t0002g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.250-10012C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720582 | ||||||
chr8:42720596
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-9998T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720596 | ||||||
chr8:42720688
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.250-9906C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720688 | ||||||
chr8:42720775
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-9819C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720775 | ||||||
chr8:42720780
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-9814G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720780 | ||||||
chr8:42720816
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-9778G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42720816 | ||||||
chr8:42721161
|
C | T | 1 | a0002c0002t0004g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.250-9433C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721161 | ||||||
chr8:42721411
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-9183C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721411 | ||||||
chr8:42721445
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-9149C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721445 | ||||||
chr8:42721450
|
G | A | 1 | a0001c0001t0002g0217 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.250-9144G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721450 | ||||||
chr8:42721510
|
C | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-9084C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721510 | ||||||
chr8:42721607
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0112a0001c0001t0001g0137others(1): Show | 5 | HG02015.hp2 HG02523.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-8987C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721607 | ||||||
chr8:42721671
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-8923C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721671 | ||||||
chr8:42721722
|
C | CAAACA | 11 | a0001c0001t0001g0034a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG01074.hp2 HG01891.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-8836_250-8832d others(7): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42721722 | |||||
chr8:42721722
|
CAAACA | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(200): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.250-8836_250-8832d others(7): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42721722 | |||||
chr8:42721722
|
CAAACAAA others(3): Show |
C | 1 | a0001c0001t0002g0004 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.250-8841_250-8832d others(12): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42721722 | |||||
chr8:42721722
|
CAAACAAA others(8): Show |
C | 2 | a0001c0001t0001g0097a0001c0001t0001g0104 | 2 | HG02004.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.250-8846_250-8832d others(17): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42721722 | |||||
chr8:42721843
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.250-8751A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721843 | ||||||
chr8:42721945
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-8649C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42721945 | ||||||
chr8:42722029
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.250-8565A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722029 | ||||||
chr8:42722075
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-8519C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722075 | ||||||
chr8:42722116
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-8478G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722116 | ||||||
chr8:42722120
|
T | C | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-8474T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722120 | ||||||
chr8:42722128
|
C | A | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00673.hp1 HG01192.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.250-8466C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722128 | ||||||
chr8:42722142
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.250-8452G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722142 | ||||||
chr8:42722267
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-8327G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722267 | ||||||
chr8:42722297
|
G | A | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-8297G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722297 | ||||||
chr8:42722382
|
G | GA | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-8202dupA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42722382 | |||||
chr8:42722540
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.250-8054A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722540 | ||||||
chr8:42722543
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-8051C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722543 | ||||||
chr8:42722561
|
G | A | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-8033G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722561 | ||||||
chr8:42722621
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-7973G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722621 | ||||||
chr8:42722811
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-7783A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722811 | ||||||
chr8:42722827
|
C | T | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-7767C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722827 | ||||||
chr8:42722878
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-7716G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722878 | ||||||
chr8:42722916
|
T | G | 115 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.250-7678T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722916 | ||||||
chr8:42722917
|
A | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-7677A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722917 | ||||||
chr8:42722918
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-7676T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42722918 | ||||||
chr8:42723024
|
TAATAAGA others(74): Show |
T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-7565_250-7485d others(83): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42723024 | |||||
chr8:42723029
|
A | G | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-7565A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723029 | ||||||
chr8:42723039
|
T | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-7555T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723039 | ||||||
chr8:42723065
|
TAATAGGA others(33): Show |
T | 19 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0055others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.250-7488_250-7449d others(42): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42723065 | |||||
chr8:42723159
|
A | AT | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-7435_250-7434i others(3): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723159 | ||||||
chr8:42723166
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0044others(22): Show | 26 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.250-7428A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723166 | ||||||
chr8:42723201
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0011g0101 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.250-7393C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723201 | ||||||
chr8:42723204
|
A | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-7390A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723204 | ||||||
chr8:42723347
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-7247C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723347 | ||||||
chr8:42723348
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.250-7246T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723348 | ||||||
chr8:42723597
|
C | G | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-6997C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723597 | ||||||
chr8:42723644
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-6950C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723644 | ||||||
chr8:42723699
|
C | T | 4 | a0002c0002t0004g0124a0002c0002t0004g0125a0002c0002t0004g0126others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-6895C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723699 | ||||||
chr8:42723882
|
T | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.250-6712T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723882 | ||||||
chr8:42723884
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-6710A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723884 | ||||||
chr8:42723888
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.250-6706C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723888 | ||||||
chr8:42723905
|
G | A | 1 | a0001c0001t0010g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.250-6689G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42723905 | ||||||
chr8:42724042
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-6552C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724042 | ||||||
chr8:42724060
|
T | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.250-6534T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724060 | ||||||
chr8:42724090
|
AAAAAAG | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-6493_250-6488d others(8): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42724090 | |||||
chr8:42724134
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-6460T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724134 | ||||||
chr8:42724299
|
A | G | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-6295A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724299 | ||||||
chr8:42724490
|
A | G | 1 | a0001c0001t0002g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.250-6104A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724490 | ||||||
chr8:42724535
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-6059C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724535 | ||||||
chr8:42724546
|
G | A | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0267others(4): Show | 7 | HG00673.hp1 HG02523.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-6048G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724546 | ||||||
chr8:42724584
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-6010C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724584 | ||||||
chr8:42724593
|
C | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-6001C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724593 | ||||||
chr8:42724596
|
T | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.250-5998T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724596 | ||||||
chr8:42724745
|
G | A | 1 | a0002c0002t0004g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.250-5849G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724745 | ||||||
chr8:42724915
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.250-5679G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42724915 | ||||||
chr8:42724917
|
AG | A | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00673.hp1 HG01192.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.250-5675delG | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42724917 | |||||
chr8:42725025
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG01243.hp2 HG01433.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-5569C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725025 | ||||||
chr8:42725065
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-5529C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725065 | ||||||
chr8:42725089
|
CTTT | C | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-5490_250-5488d others(5): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42725089 | |||||
chr8:42725232
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-5362A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725232 | ||||||
chr8:42725253
|
C | T | 12 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 13 | HG01243.hp1 HG02615.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-5341C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725253 | ||||||
chr8:42725317
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-5277T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725317 | ||||||
chr8:42725423
|
T | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-5171T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725423 | ||||||
chr8:42725529
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-5065G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725529 | ||||||
chr8:42725584
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-5010T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725584 | ||||||
chr8:42725641
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.250-4953C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725641 | ||||||
chr8:42725676
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4918C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725676 | ||||||
chr8:42725768
|
G | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4826G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725768 | ||||||
chr8:42725908
|
G | T | 1 | a0001c0001t0003g0033 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.250-4686G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725908 | ||||||
chr8:42725937
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4657G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725937 | ||||||
chr8:42725938
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0091a0001c0001t0001g0092 | 3 | HG02280.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.250-4656C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42725938 | ||||||
chr8:42726099
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4495T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726099 | ||||||
chr8:42726207
|
A | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4387A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726207 | ||||||
chr8:42726304
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-4290G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726304 | ||||||
chr8:42726407
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4187C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726407 | ||||||
chr8:42726414
|
A | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4180A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726414 | ||||||
chr8:42726425
|
A | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4169A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726425 | ||||||
chr8:42726480
|
C | CT | 13 | a0001c0001t0001g0035a0001c0003t0001g0141a0001c0003t0001g0142others(10): Show | 13 | HG00438.hp2 HG01074.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.250-4097dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42726480 | |||||
chr8:42726480
|
CT | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(191): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.250-4097delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42726480 | |||||
chr8:42726480
|
CTT | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 9 | HG01243.hp1 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-4098_250-4097d others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42726480 | |||||
chr8:42726509
|
TAGCTCTG others(13): Show |
T | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.250-4069_250-4050d others(22): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42726509 | |||||
chr8:42726603
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3991G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726603 | ||||||
chr8:42726647
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3947C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726647 | ||||||
chr8:42726680
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.250-3914G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42726680 | ||||||
chr8:42727038
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3556T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727038 | ||||||
chr8:42727170
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.250-3424C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727170 | ||||||
chr8:42727201
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3393T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727201 | ||||||
chr8:42727230
|
G | A | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-3364G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727230 | ||||||
chr8:42727364
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.250-3230C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727364 | ||||||
chr8:42727372
|
CG | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3221delG | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727372 | ||||||
chr8:42727373
|
GA | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(71): Show | 76 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.250-3204delA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42727373 | |||||
chr8:42727374
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.250-3220A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727374 | ||||||
chr8:42727377
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3217A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727377 | ||||||
chr8:42727436
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.250-3158G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727436 | ||||||
chr8:42727440
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3154A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727440 | ||||||
chr8:42727449
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3145C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727449 | ||||||
chr8:42727554
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-3040T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727554 | ||||||
chr8:42727589
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-3005C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727589 | ||||||
chr8:42727680
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.250-2914T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727680 | ||||||
chr8:42727707
|
A | G | 1 | a0002c0002t0004g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.250-2887A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727707 | ||||||
chr8:42727718
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.250-2876C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727718 | ||||||
chr8:42727756
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0002g0210 | 2 | HG02809.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.250-2838G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727756 | ||||||
chr8:42727812
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(36): Show | 41 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.250-2782G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727812 | ||||||
chr8:42727816
|
C | T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-2778C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727816 | ||||||
chr8:42727898
|
C | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-2696C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727898 | ||||||
chr8:42727909
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.250-2685C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42727909 | ||||||
chr8:42728028
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-2566A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728028 | ||||||
chr8:42728331
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-2263T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728331 | ||||||
chr8:42728348
|
G | C | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.250-2246G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728348 | ||||||
chr8:42728447
|
T | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-2147T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728447 | ||||||
chr8:42728521
|
C | G | 1 | a0001c0001t0002g0190 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.250-2073C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728521 | ||||||
chr8:42728698
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-1896A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728698 | ||||||
chr8:42728699
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-1895G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728699 | ||||||
chr8:42728716
|
A | C | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-1878A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728716 | ||||||
chr8:42728807
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.250-1787G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728807 | ||||||
chr8:42728847
|
G | T | 5 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(2): Show | 5 | HG02055.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-1747G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728847 | ||||||
chr8:42728908
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.250-1686G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728908 | ||||||
chr8:42728973
|
A | G | 1 | a0001c0001t0002g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.250-1621A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728973 | ||||||
chr8:42728992
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-1602T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42728992 | ||||||
chr8:42729073
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.250-1521G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729073 | ||||||
chr8:42729122
|
C | G | 1 | a0001c0001t0002g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.250-1472C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729122 | ||||||
chr8:42729136
|
G | A | 115 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(112): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.250-1458G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729136 | ||||||
chr8:42729161
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0227 | 2 | HG00738.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.250-1433A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729161 | ||||||
chr8:42729178
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.250-1416C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729178 | ||||||
chr8:42729261
|
T | A | 1 | a0001c0001t0002g0004 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.250-1333T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729261 | ||||||
chr8:42729266
|
C | A | 7 | a0001c0001t0002g0251a0001c0001t0005g0157a0001c0001t0005g0186others(4): Show | 7 | HG00280.hp2 HG01261.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-1328C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729266 | ||||||
chr8:42729367
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-1227A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729367 | ||||||
chr8:42729396
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250-1198C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729396 | ||||||
chr8:42729404
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-1190T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729404 | ||||||
chr8:42729602
|
A | T | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-992A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729602 | ||||||
chr8:42729849
|
C | T | 1 | a0002c0002t0004g0123 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250-745C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729849 | ||||||
chr8:42729921
|
TA | T | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-669delA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 42729921 | |||||
chr8:42729936
|
G | A | 1 | a0002c0002t0004g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.250-658G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729936 | ||||||
chr8:42729960
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.250-634G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42729960 | ||||||
chr8:42730082
|
A | G | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-512A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730082 | ||||||
chr8:42730154
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-440A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730154 | ||||||
chr8:42730157
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-437T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730157 | ||||||
chr8:42730167
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.250-427G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730167 | ||||||
chr8:42730191
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.250-403C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730191 | ||||||
chr8:42730203
|
T | A | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-391T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730203 | ||||||
chr8:42730463
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-131G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730463 | ||||||
chr8:42730474
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.250-120G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730474 | ||||||
chr8:42730551
|
T | C | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-43T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 3/5 | chr8 | 42730551 | ||||||
chr8:42730750
|
TTAAAAAG others(338): Show |
T | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.359+66_359+410del | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 42730750 | |||||
chr8:42730905
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.359+202G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42730905 | ||||||
chr8:42730921
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.359+218G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42730921 | ||||||
chr8:42731006
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359+303C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42731006 | ||||||
chr8:42731017
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.359+314C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42731017 | ||||||
chr8:42731024
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.359+321C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42731024 | ||||||
chr8:42731033
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.359+330C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42731033 | ||||||
chr8:42731057
|
A | AAAAT | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0002g0253 | 3 | HG00741.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.359+386_359+389dup others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 42731057 | |||||
chr8:42731057
|
AAAAT | A | 248 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(245): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.359+386_359+389del others(4): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 42731057 | |||||
chr8:42731089
|
T | A | 1 | a0001c0001t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.359+386T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42731089 | ||||||
chr8:42731113
|
G | A | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.359+410G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42731113 | ||||||
chr8:42731215
|
T | TA | 4 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0094others(1): Show | 4 | HG01167.hp2 HG02602.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.360-445dupA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 42731215 | |||||
chr8:42731504
|
G | A | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.360-163G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 4/5 | chr8 | 42731504 | ||||||
chr8:42732653
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(216): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1242+104G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42732653 | ||||||
chr8:42732676
|
A | G | 1 | a0001c0001t0002g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1242+127A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42732676 | ||||||
chr8:42732719
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1242+170T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42732719 | ||||||
chr8:42732776
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1242+227T>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42732776 | ||||||
chr8:42732895
|
G | C | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1242+346G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42732895 | ||||||
chr8:42733125
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1242+576A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733125 | ||||||
chr8:42733324
|
G | A | 3 | a0001c0001t0002g0153a0001c0001t0002g0202a0001c0001t0002g0219 | 3 | HG00597.hp1 NA18953.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1242+775G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733324 | ||||||
chr8:42733358
|
A | C | 1 | a0001c0001t0002g0187 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1242+809A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733358 | ||||||
chr8:42733500
|
A | C | 1 | a0001c0001t0002g0185 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1242+951A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733500 | ||||||
chr8:42733592
|
C | CT | 17 | a0001c0001t0001g0059a0001c0001t0001g0130a0001c0001t0002g0171others(14): Show | 18 | HG00735.hp2 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1242+1064dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 42733592 | |||||
chr8:42733592
|
CT | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(66): Show | 71 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1242+1064delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 42733592 | |||||
chr8:42733597
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1242+1048T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733597 | ||||||
chr8:42733617
|
A | AT | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(271): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1242+1068_1242+106 others(5): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733617 | ||||||
chr8:42733617
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1242+1068A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733617 | ||||||
chr8:42733653
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(269): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1242+1104T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733653 | ||||||
chr8:42733712
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0177a0001c0001t0002g0178others(2): Show | 5 | HG00621.hp1 HG02015.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1242+1163C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733712 | ||||||
chr8:42733948
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1242+1399G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733948 | ||||||
chr8:42733985
|
C | T | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1242+1436C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42733985 | ||||||
chr8:42734021
|
G | A | 2 | a0001c0004t0007g0025a0001c0004t0007g0026 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1242+1472G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734021 | ||||||
chr8:42734026
|
G | A | 3 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | HG03710.hp2 HG03942.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1242+1477G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734026 | ||||||
chr8:42734034
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1242+1485G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734034 | ||||||
chr8:42734128
|
A | T | 11 | a0001c0004t0007g0025a0001c0004t0007g0026a0002c0002t0004g0119others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1242+1579A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734128 | ||||||
chr8:42734229
|
C | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143 | 3 | HG01074.hp2 HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1242+1680C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734229 | ||||||
chr8:42734259
|
C | CA | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(101): Show | 107 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1242+1734dupA | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 42734259 | |||||
chr8:42734259
|
C | CAA | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(12): Show | 15 | HG00735.hp1 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1242+1733_1242+173 others(6): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 42734259 | |||||
chr8:42734259
|
CAA | C | 6 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1242+1733_1242+173 others(6): Show |
CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 42734259 | |||||
chr8:42734268
|
A | G | 1 | a0001c0001t0002g0202 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1242+1719A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734268 | ||||||
chr8:42734329
|
G | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(270): Show | 279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.1242+1780G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734329 | ||||||
chr8:42734352
|
A | G | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1242+1803A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734352 | ||||||
chr8:42734418
|
G | T | 1 | a0001c0001t0006g0243 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1242+1869G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734418 | ||||||
chr8:42734420
|
A | AT | 7 | a0001c0001t0001g0059a0001c0001t0001g0098a0001c0001t0001g0270others(4): Show | 7 | HG00544.hp1 HG01433.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1242+1888dupT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 42734420 | |||||
chr8:42734420
|
AT | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0075a0001c0001t0001g0076others(4): Show | 7 | HG02622.hp1 HG02818.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1242+1888delT | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 42734420 | |||||
chr8:42734459
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(156): Show | 163 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1242+1910A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734459 | ||||||
chr8:42734462
|
G | C | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1242+1913G>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734462 | ||||||
chr8:42734473
|
G | T | 56 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0042others(53): Show | 57 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1242+1924G>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734473 | ||||||
chr8:42734516
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1242+1967T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734516 | ||||||
chr8:42734565
|
A | G | 14 | a0001c0003t0001g0141a0001c0003t0001g0142a0001c0003t0001g0143others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1243-1919A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734565 | ||||||
chr8:42734644
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1243-1840T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734644 | ||||||
chr8:42734759
|
C | T | 1 | a0001c0001t0009g0229 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1243-1725C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734759 | ||||||
chr8:42734765
|
C | A | 1 | a0001c0001t0002g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1243-1719C>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734765 | ||||||
chr8:42734928
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0023 | 2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1243-1556C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734928 | ||||||
chr8:42734986
|
C | G | 1 | a0001c0001t0002g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1243-1498C>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42734986 | ||||||
chr8:42735014
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1243-1470A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735014 | ||||||
chr8:42735077
|
G | A | 1 | a0001c0001t0006g0243 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1243-1407G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735077 | ||||||
chr8:42735217
|
C | T | 1 | a0001c0001t0002g0258 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1243-1267C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735217 | ||||||
chr8:42735526
|
A | G | 14 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(11): Show | 15 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1243-958A>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735526 | ||||||
chr8:42735597
|
G | A | 9 | a0002c0002t0004g0119a0002c0002t0004g0120a0002c0002t0004g0121others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1243-887G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735597 | ||||||
chr8:42735721
|
A | C | 7 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG02280.hp2 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1243-763A>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735721 | ||||||
chr8:42735899
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0066 | 3 | NA18967.hp1 NA18969.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1243-585C>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735899 | ||||||
chr8:42735951
|
T | C | 23 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(20): Show | 24 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1243-533T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42735951 | ||||||
chr8:42736162
|
T | C | 58 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0042others(55): Show | 59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1243-322T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42736162 | ||||||
chr8:42736167
|
T | C | 14 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(11): Show | 15 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1243-317T>C | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42736167 | ||||||
chr8:42736296
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1243-188T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42736296 | ||||||
chr8:42736345
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1243-139G>A | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42736345 | ||||||
chr8:42736378
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1243-106A>T | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42736378 | ||||||
chr8:42736413
|
T | G | 23 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0009others(20): Show | 24 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1243-71T>G | CHRNB3 | ENSG00000147432.7 | transcript | ENST00000289957.3 | protein_coding | 5/5 | chr8 | 42736413 |