geneid | 146227 |
---|---|
ensemblid | ENSG00000166546.15 |
hgncid | 24160 |
symbol | BEAN1 |
name | brain expressed associated with NEDD4 1 |
refseq_nuc | NM_001178020.3 |
refseq_prot | NP_001171491.1 |
ensembl_nuc | ENST00000536005.7 |
ensembl_prot | ENSP00000442793.2 |
mane_status | MANE Select |
chr | chr16 |
start | 66427295 |
end | 66482833 |
strand | + |
ver | v1.2 |
region | chr16:66427295-66482833 |
region5000 | chr16:66422295-66487833 |
regionname0 | BEAN1_chr16_66427295_66482833 |
regionname5000 | BEAN1_chr16_66422295_66487833 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 259 | 291 | 85 | 52 | 110 | 9 | 34 | 76 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0002 | 0/0 | 259 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0003 | 0/1 | 259 | 2 | 0 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0004 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0005 | 0/0 | 259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0006 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 780 | 289 | 85 | 51 | 109 | 9 | 34 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
c0002 | 0/1 | 780 | 2 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
c0003 | 0/0 | 780 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
c0004 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
c0005 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
c0006 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
c0007 | 0/0 | 780 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
c0008 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2128 | 180 | 40 | 35 | 69 | 7 | 27 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0002 | 0/0 | 2128 | 47 | 11 | 5 | 24 | 1 | 6 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0003 | 0/0 | 2128 | 44 | 15 | 9 | 19 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0004 | 0/0 | 2128 | 15 | 13 | 2 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0005 | 0/0 | 2128 | 2 | 0 | 0 | 0 | 2 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0006 | 0/0 | 2128 | 2 | 1 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0007 | 0/0 | 2128 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0008 | 0/0 | 2128 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0009 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0010 | 0/0 | 2128 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0011 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
t0012 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 780 | 289 | 85 | 51 | 109 | 9 | 34 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0005 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0007 | 0/0 | 780 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0002c0003 | 0/0 | 780 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0003c0002 | 0/1 | 780 | 2 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0004c0006 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0005c0004 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0006c0008 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2907 | 175 | 40 | 35 | 66 | 6 | 27 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0002 | 0/0 | 2907 | 45 | 11 | 5 | 22 | 1 | 6 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0003 | 0/0 | 2907 | 42 | 14 | 8 | 19 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0004 | 0/0 | 2907 | 15 | 13 | 2 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0005 | 0/0 | 2907 | 2 | 0 | 0 | 0 | 2 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0006 | 0/0 | 2907 | 2 | 1 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0007 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0008 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0009 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0010 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0011 | 0/0 | 2947 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0001t0012 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0005t0001 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0001c0007t0003 | 0/0 | 2907 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0002c0003t0002 | 0/0 | 2907 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0003c0002t0001 | 0/1 | 2907 | 2 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0004c0006t0001 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0005c0004t0003 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
a0006c0008t0001 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | copy fasta | chr16 | 66422295 | 66487833 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0011g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0005t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0007t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0002c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0003c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0004c0006t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0005c0004t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0006c0008t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0005 | g0087 | EUR | GBR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00140 | hp2 | a0003 | c0002 | t0001 | g0188 | EUR | GBR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00609 | hp1 | a0006 | c0008 | t0001 | g0050 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01175 | hp2 | a0001 | c0007 | t0003 | g0245 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0277 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0231 | EUR | IBS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02071 | hp2 | a0004 | c0006 | t0001 | g0187 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0105 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03041 | hp1 | a0005 | c0004 | t0003 | g0197 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18984 | hp1 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19007 | hp1 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19011 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19068 | hp1 | a0002 | c0003 | t0002 | g0158 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19082 | hp1 | a0001 | c0005 | t0001 | g0200 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ASW | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ASW | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | GIH | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
homoSapiens_chm13v2 | hp1 | a0003 | c0002 | t0001 | g0089 | REF | REF | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0126 | REF | REF | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66469781
|
C | T | 1 | a0006 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.205C>T | p.Arg69Trp | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/5 | 424/2907 | 205/780 | 69/259 | chr16 | 66469781 | ||
chr16:66469802
|
C | A | 1 | a0003 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.226C>A | p.Arg76Ser | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/5 | 445/2907 | 226/780 | 76/259 | chr16 | 66469802 | ||
chr16:66477657
|
C | A | 1 | a0005 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.387C>A | p.Asp129Glu | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/5 | 606/2907 | 387/780 | 129/259 | chr16 | 66477657 | ||
chr16:66480636
|
A | G | 1 | a0004 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.491A>G | p.Asp164Gly | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 710/2907 | 491/780 | 164/259 | chr16 | 66480636 | ||
chr16:66480709
|
C | G | 1 | a0002 | 2 | NA19007.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.564C>G | p.His188Gln | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 783/2907 | 564/780 | 188/259 | chr16 | 66480709 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66477657
|
C | T | 1 | a0001c0007 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.387C>T | p.Asp129Asp | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/5 | 606/2907 | 387/780 | 129/259 | chr16 | 66477657 | ||
chr16:66480841
|
G | A | 1 | a0001c0005 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.696G>A | p.Pro232Pro | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 915/2907 | 696/780 | 232/259 | chr16 | 66480841 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66427314
|
G | T | 2 | a0001c0001t0007a0001c0001t0008 | 4 | HG03209.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-200G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/5 | 10363 | chr16 | 66427314 | |||||
chr16:66481059
|
C | T | 4 | a0001c0001t0003a0001c0001t0008a0001c0007t0003others(1): Show | 46 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*134C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 134 | chr16 | 66481059 | |||||
chr16:66481217
|
G | A | 2 | a0001c0001t0002a0002c0003t0002 | 47 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*292G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 292 | chr16 | 66481217 | |||||
chr16:66481323
|
A | G | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 398 | chr16 | 66481323 | |||||
chr16:66481349
|
G | T | 1 | a0001c0001t0004 | 15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*424G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 424 | chr16 | 66481349 | |||||
chr16:66481431
|
G | A | 1 | a0001c0001t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 506 | chr16 | 66481431 | |||||
chr16:66481460
|
C | T | 1 | a0001c0001t0006 | 2 | HG02886.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*535C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 535 | chr16 | 66481460 | |||||
chr16:66481753
|
G | A | 1 | a0001c0001t0010 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 828 | chr16 | 66481753 | |||||
chr16:66482130
|
G | A | 1 | a0001c0001t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1205 | chr16 | 66482130 | |||||
chr16:66482344
|
T | C | 1 | a0001c0001t0005 | 2 | HG00140.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1419T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1419 | chr16 | 66482344 | |||||
chr16:66482666
|
G | GGGAAAAA others(33): Show |
1 | a0001c0001t0011 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1742_*1781dupGGAA others(36): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1782 | INFO_REALIGN_3_PRIME | chr16 | 66482666 | ||||
chr16:66482676
|
G | A | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1751G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1751 | chr16 | 66482676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66427531
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-83+100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427531 | ||||||
chr16:66427648
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-83+217G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427648 | ||||||
chr16:66427694
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-83+263G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427694 | ||||||
chr16:66427705
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-83+274T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427705 | ||||||
chr16:66428024
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-83+593G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428024 | ||||||
chr16:66428057
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-83+626A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428057 | ||||||
chr16:66428124
|
G | T | 2 | a0001c0001t0001g0283a0001c0001t0006g0284 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-83+693G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428124 | ||||||
chr16:66428210
|
C | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-83+779C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428210 | ||||||
chr16:66428311
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-83+880C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428311 | ||||||
chr16:66429054
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-83+1623C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429054 | ||||||
chr16:66429145
|
G | T | 3 | a0001c0001t0002g0279a0001c0001t0002g0280a0001c0001t0003g0278 | 3 | HG02129.hp2 NA18963.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-83+1714G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429145 | ||||||
chr16:66429157
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(95): Show | 104 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-83+1726G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429157 | ||||||
chr16:66429232
|
C | T | 3 | a0001c0001t0003g0104a0001c0001t0003g0106a0001c0001t0012g0105 | 3 | HG01884.hp1 HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-83+1801C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429232 | ||||||
chr16:66429531
|
T | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-83+2100T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429531 | ||||||
chr16:66429607
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-83+2176C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429607 | ||||||
chr16:66429838
|
AAC | A | 22 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(19): Show | 23 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-83+2411_-83+2412d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66429838 | |||||
chr16:66430210
|
C | G | 3 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0102 | 5 | HG00738.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-83+2779C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430210 | ||||||
chr16:66430210
|
C | T | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-83+2779C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430210 | ||||||
chr16:66430776
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(87): Show | 96 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-83+3345G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430776 | ||||||
chr16:66430977
|
C | A | 21 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(18): Show | 22 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.-83+3546C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430977 | ||||||
chr16:66431278
|
C | T | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-83+3847C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431278 | ||||||
chr16:66431603
|
G | GT | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-83+4183dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66431603 | |||||
chr16:66431603
|
GT | G | 22 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 23 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.-83+4183delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66431603 | |||||
chr16:66431635
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-83+4204C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431635 | ||||||
chr16:66431660
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-83+4229A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431660 | ||||||
chr16:66431869
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-83+4438C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431869 | ||||||
chr16:66431876
|
G | A | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-83+4445G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431876 | ||||||
chr16:66432459
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-83+5028C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432459 | ||||||
chr16:66432570
|
C | T | 1 | a0001c0001t0004g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82-5025C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432570 | ||||||
chr16:66432635
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(196): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-82-4960A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432635 | ||||||
chr16:66432685
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-82-4910C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432685 | ||||||
chr16:66432736
|
A | G | 2 | a0001c0001t0001g0283a0001c0001t0006g0284 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-82-4859A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432736 | ||||||
chr16:66432742
|
T | C | 20 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(17): Show | 21 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82-4853T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432742 | ||||||
chr16:66432791
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-82-4804G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432791 | ||||||
chr16:66433100
|
TTTATTTT others(2): Show |
T | 4 | a0001c0001t0002g0092a0001c0001t0002g0279a0001c0001t0002g0280others(1): Show | 4 | HG02129.hp2 NA18963.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82-4477_-82-4469d others(11): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66433100 | |||||
chr16:66433366
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-82-4229C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433366 | ||||||
chr16:66433392
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-82-4203G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433392 | ||||||
chr16:66433548
|
G | A | 22 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0136others(19): Show | 23 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-82-4047G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433548 | ||||||
chr16:66433558
|
CCTTCCTA others(9): Show |
C | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-82-4036_-82-4021d others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433558 | ||||||
chr16:66433584
|
A | AAGCCAAT | 24 | a0001c0001t0001g0036a0001c0001t0001g0257a0001c0001t0001g0258others(21): Show | 25 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.-82-4010_-82-4009i others(9): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66433584 | |||||
chr16:66433985
|
C | T | 18 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0264others(15): Show | 19 | HG00642.hp2 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-82-3610C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433985 | ||||||
chr16:66434156
|
G | A | 1 | a0001c0001t0003g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-82-3439G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434156 | ||||||
chr16:66434197
|
G | A | 20 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 21 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-82-3398G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434197 | ||||||
chr16:66434206
|
CCCCCGAC others(11): Show |
C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82-3372_-82-3355d others(20): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66434206 | |||||
chr16:66434219
|
C | T | 16 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 17 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-82-3376C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434219 | ||||||
chr16:66434319
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0011g0277 | 2 | HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-82-3276G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434319 | ||||||
chr16:66434450
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0003g0256 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-82-3145G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434450 | ||||||
chr16:66434609
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(185): Show | 197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.-82-2986T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434609 | ||||||
chr16:66434669
|
G | A | 9 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168others(6): Show | 9 | HG00673.hp1 HG02165.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.-82-2926G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434669 | ||||||
chr16:66434716
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(95): Show | 104 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-82-2879G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434716 | ||||||
chr16:66434785
|
T | G | 4 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0008g0006others(1): Show | 5 | HG02109.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82-2810T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434785 | ||||||
chr16:66435040
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG01169.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-82-2555G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435040 | ||||||
chr16:66435068
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-82-2527G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435068 | ||||||
chr16:66435241
|
G | C | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(39): Show | 45 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.-82-2354G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435241 | ||||||
chr16:66435372
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-82-2223A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435372 | ||||||
chr16:66435404
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-82-2191T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435404 | ||||||
chr16:66435577
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-82-2018T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435577 | ||||||
chr16:66435651
|
A | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(192): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-82-1944A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435651 | ||||||
chr16:66435812
|
G | A | 29 | a0001c0001t0001g0034a0001c0001t0001g0110a0001c0001t0001g0111others(26): Show | 30 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.-82-1783G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435812 | ||||||
chr16:66435897
|
T | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG01169.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-82-1698T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435897 | ||||||
chr16:66436087
|
C | G | 24 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0253others(21): Show | 25 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-82-1508C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436087 | ||||||
chr16:66436266
|
C | CT | 98 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0032others(95): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-82-1310dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66436266 | |||||
chr16:66436330
|
T | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82-1265T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436330 | ||||||
chr16:66436443
|
A | AT | 28 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0130others(25): Show | 29 | HG00544.hp1 HG00642.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82-1136dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66436443 | |||||
chr16:66436513
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0130 | 2 | HG03927.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-82-1082T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436513 | ||||||
chr16:66436558
|
G | T | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-82-1037G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436558 | ||||||
chr16:66436559
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-82-1036T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436559 | ||||||
chr16:66436580
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0002g0211 | 2 | NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-82-1015T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436580 | ||||||
chr16:66436829
|
T | C | 5 | a0001c0001t0001g0046a0001c0001t0001g0157a0001c0001t0002g0044others(2): Show | 5 | NA18953.hp1 NA19003.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82-766T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436829 | ||||||
chr16:66436919
|
A | G | 23 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0253others(20): Show | 24 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-82-676A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436919 | ||||||
chr16:66437104
|
G | GTAA | 14 | a0001c0001t0001g0034a0001c0001t0001g0110a0001c0001t0001g0111others(11): Show | 14 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-82-470_-82-468dup others(3): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66437104 | |||||
chr16:66437270
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0037others(69): Show | 75 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-82-325G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437270 | ||||||
chr16:66437280
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.-82-315G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437280 | ||||||
chr16:66437314
|
T | C | 1 | a0001c0001t0003g0160 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-82-281T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437314 | ||||||
chr16:66437328
|
C | CCACT | 195 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(192): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-82-265_-82-264ins others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66437328 | |||||
chr16:66437371
|
C | T | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82-224C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437371 | ||||||
chr16:66437544
|
C | A | 75 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0034others(72): Show | 80 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-82-51C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437544 | ||||||
chr16:66437857
|
G | A | 5 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0003g0137others(2): Show | 5 | HG00733.hp1 HG01099.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+156G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66437857 | ||||||
chr16:66438067
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0283 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+366G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438067 | ||||||
chr16:66438106
|
C | T | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+405C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438106 | ||||||
chr16:66438149
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+448C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438149 | ||||||
chr16:66438213
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.25+512G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438213 | ||||||
chr16:66438239
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+538C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438239 | ||||||
chr16:66438257
|
G | A | 2 | a0001c0001t0003g0124a0001c0001t0009g0019 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.25+556G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438257 | ||||||
chr16:66438257
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+556G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438257 | ||||||
chr16:66438263
|
A | G | 4 | a0001c0001t0001g0125a0001c0001t0007g0108a0001c0001t0007g0109others(1): Show | 5 | HG03209.hp1 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+562A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438263 | ||||||
chr16:66438332
|
C | T | 2 | a0001c0001t0003g0153a0001c0001t0003g0278 | 2 | NA18963.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.25+631C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438332 | ||||||
chr16:66438333
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+632G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438333 | ||||||
chr16:66438345
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.25+644T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438345 | ||||||
chr16:66438375
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25+674C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438375 | ||||||
chr16:66438530
|
C | T | 22 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0144others(19): Show | 23 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.25+829C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438530 | ||||||
chr16:66438575
|
C | T | 23 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0253others(20): Show | 24 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+874C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438575 | ||||||
chr16:66438602
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(97): Show | 106 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.25+901G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438602 | ||||||
chr16:66438721
|
T | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0032others(83): Show | 91 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.25+1020T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438721 | ||||||
chr16:66438734
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.25+1033C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438734 | ||||||
chr16:66438806
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.25+1105C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438806 | ||||||
chr16:66438806
|
C | T | 23 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0253others(20): Show | 24 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+1105C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438806 | ||||||
chr16:66438809
|
C | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0283 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+1108C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438809 | ||||||
chr16:66438811
|
C | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+1110C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438811 | ||||||
chr16:66439485
|
G | C | 69 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(66): Show | 74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.25+1784G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439485 | ||||||
chr16:66439548
|
C | T | 3 | a0001c0001t0007g0108a0001c0001t0007g0109a0001c0001t0008g0006 | 4 | HG03209.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1847C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439548 | ||||||
chr16:66439609
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0128 | 2 | HG01109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.25+1908G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439609 | ||||||
chr16:66439612
|
G | GT | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0032others(68): Show | 76 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.25+1912dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66439612 | |||||
chr16:66439723
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.25+2022G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439723 | ||||||
chr16:66439801
|
G | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0283 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+2100G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439801 | ||||||
chr16:66439830
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0082 | 2 | HG03927.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.25+2129A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439830 | ||||||
chr16:66439838
|
C | A | 1 | a0001c0001t0001g0165 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.25+2137C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439838 | ||||||
chr16:66439990
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0283 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+2289C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439990 | ||||||
chr16:66440043
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+2342A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440043 | ||||||
chr16:66440123
|
CT | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(125): Show | 134 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.25+2446delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66440123 | |||||
chr16:66440123
|
CTT | C | 69 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(66): Show | 75 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.25+2445_25+2446del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66440123 | |||||
chr16:66440123
|
CTTT | C | 9 | a0001c0001t0001g0036a0001c0001t0001g0221a0001c0001t0001g0222others(6): Show | 9 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+2444_25+2446del others(3): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66440123 | |||||
chr16:66440129
|
T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+2428T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440129 | ||||||
chr16:66440162
|
C | A | 2 | a0001c0001t0001g0246a0001c0001t0002g0251 | 2 | NA18942.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.25+2461C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440162 | ||||||
chr16:66440255
|
A | G | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0032others(81): Show | 89 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.25+2554A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440255 | ||||||
chr16:66440369
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.25+2668G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440369 | ||||||
chr16:66440393
|
A | G | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0096others(39): Show | 45 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.25+2692A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440393 | ||||||
chr16:66440572
|
A | T | 6 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2871A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440572 | ||||||
chr16:66440576
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+2875T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440576 | ||||||
chr16:66440594
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2893G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440594 | ||||||
chr16:66440653
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+2952A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440653 | ||||||
chr16:66440717
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3016A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440717 | ||||||
chr16:66440722
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3021A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440722 | ||||||
chr16:66440724
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3023T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440724 | ||||||
chr16:66440734
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3033G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440734 | ||||||
chr16:66440735
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3034G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440735 | ||||||
chr16:66440737
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3036T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440737 | ||||||
chr16:66440747
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3046T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440747 | ||||||
chr16:66440751
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3050T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440751 | ||||||
chr16:66440764
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3063T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440764 | ||||||
chr16:66440765
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3064G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440765 | ||||||
chr16:66440768
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3067T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440768 | ||||||
chr16:66440769
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3068G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440769 | ||||||
chr16:66440773
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3072T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440773 | ||||||
chr16:66440774
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3073G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440774 | ||||||
chr16:66440776
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3075G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440776 | ||||||
chr16:66440779
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3078G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440779 | ||||||
chr16:66440792
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3091A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440792 | ||||||
chr16:66440795
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3094T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440795 | ||||||
chr16:66440796
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3095G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440796 | ||||||
chr16:66440798
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3097G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440798 | ||||||
chr16:66440799
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3098T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440799 | ||||||
chr16:66440800
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3099T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440800 | ||||||
chr16:66440804
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3103A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440804 | ||||||
chr16:66440805
|
C | T | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+3104C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440805 | ||||||
chr16:66440808
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3107G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440808 | ||||||
chr16:66440811
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3110C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440811 | ||||||
chr16:66440813
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3112A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440813 | ||||||
chr16:66440814
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3113A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440814 | ||||||
chr16:66440815
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3114A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440815 | ||||||
chr16:66440817
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3116T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440817 | ||||||
chr16:66440848
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3147T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440848 | ||||||
chr16:66440852
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3151T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440852 | ||||||
chr16:66440853
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3152T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440853 | ||||||
chr16:66440856
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3155T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440856 | ||||||
chr16:66440857
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3156T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440857 | ||||||
chr16:66440864
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3163T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440864 | ||||||
chr16:66440867
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3166T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440867 | ||||||
chr16:66440870
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3169T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440870 | ||||||
chr16:66440871
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3170T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440871 | ||||||
chr16:66440873
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3172G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440873 | ||||||
chr16:66440874
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3173G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440874 | ||||||
chr16:66440875
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3174G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440875 | ||||||
chr16:66440876
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3175G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440876 | ||||||
chr16:66440878
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3177G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440878 | ||||||
chr16:66440884
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3183G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440884 | ||||||
chr16:66440885
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3184T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440885 | ||||||
chr16:66440886
|
C | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3185C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440886 | ||||||
chr16:66440887
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3186A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440887 | ||||||
chr16:66440888
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3187G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440888 | ||||||
chr16:66440891
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3190A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440891 | ||||||
chr16:66440902
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3201A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440902 | ||||||
chr16:66440905
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3204C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440905 | ||||||
chr16:66440908
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3207A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440908 | ||||||
chr16:66440909
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3208G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440909 | ||||||
chr16:66440916
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3215T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440916 | ||||||
chr16:66440934
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3233A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440934 | ||||||
chr16:66440975
|
C | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3274C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440975 | ||||||
chr16:66440976
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3275T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440976 | ||||||
chr16:66441011
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0283 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+3310G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441011 | ||||||
chr16:66441024
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3323G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441024 | ||||||
chr16:66441025
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3324A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441025 | ||||||
chr16:66441066
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3365G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441066 | ||||||
chr16:66441067
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3366T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441067 | ||||||
chr16:66441075
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3374T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441075 | ||||||
chr16:66441107
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3406A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441107 | ||||||
chr16:66441129
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3428G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441129 | ||||||
chr16:66441135
|
A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3434A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441135 | ||||||
chr16:66441136
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3435G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441136 | ||||||
chr16:66441137
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3436T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441137 | ||||||
chr16:66441147
|
C | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(193): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.25+3446C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441147 | ||||||
chr16:66441251
|
T | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+3550T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441251 | ||||||
chr16:66441353
|
C | T | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+3652C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441353 | ||||||
chr16:66441505
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.25+3804C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441505 | ||||||
chr16:66441547
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.25+3846C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441547 | ||||||
chr16:66441712
|
A | G | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0096others(38): Show | 44 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.25+4011A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441712 | ||||||
chr16:66441873
|
C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+4172C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441873 | ||||||
chr16:66441900
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.25+4199A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441900 | ||||||
chr16:66441941
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.25+4240A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441941 | ||||||
chr16:66441970
|
C | G | 1 | a0001c0001t0002g0263 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.25+4269C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441970 | ||||||
chr16:66442042
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.25+4341A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442042 | ||||||
chr16:66442160
|
C | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0004g0002others(7): Show | 13 | HG00738.hp1 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.25+4459C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442160 | ||||||
chr16:66442172
|
C | A | 5 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+4471C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442172 | ||||||
chr16:66442215
|
G | T | 4 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+4514G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442215 | ||||||
chr16:66442474
|
C | A | 5 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+4773C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442474 | ||||||
chr16:66442662
|
A | AG | 5 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+4962dupG | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66442662 | |||||
chr16:66442764
|
T | G | 5 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+5063T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442764 | ||||||
chr16:66442770
|
G | A | 5 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+5069G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442770 | ||||||
chr16:66442832
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+5131C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442832 | ||||||
chr16:66443041
|
C | T | 106 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(103): Show | 114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.25+5340C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443041 | ||||||
chr16:66443044
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.25+5343T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443044 | ||||||
chr16:66443104
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+5403G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443104 | ||||||
chr16:66443119
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.25+5418T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443119 | ||||||
chr16:66443186
|
G | A | 4 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+5485G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443186 | ||||||
chr16:66443244
|
T | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+5543T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443244 | ||||||
chr16:66443279
|
T | C | 4 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+5578T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443279 | ||||||
chr16:66443610
|
C | A | 1 | a0001c0001t0002g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.25+5909C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443610 | ||||||
chr16:66443733
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.25+6032G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443733 | ||||||
chr16:66443796
|
T | G | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+6095T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443796 | ||||||
chr16:66443818
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6117G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443818 | ||||||
chr16:66443847
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(104): Show | 115 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.25+6146C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443847 | ||||||
chr16:66443907
|
G | C | 106 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(103): Show | 114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.25+6206G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443907 | ||||||
chr16:66443976
|
C | T | 9 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168others(6): Show | 9 | HG00673.hp1 HG02165.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+6275C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443976 | ||||||
chr16:66444272
|
A | G | 1 | a0002c0003t0002g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.25+6571A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444272 | ||||||
chr16:66444298
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.25+6597G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444298 | ||||||
chr16:66444391
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+6690C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444391 | ||||||
chr16:66444425
|
G | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.25+6724G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444425 | ||||||
chr16:66444440
|
G | A | 1 | a0001c0001t0003g0007 | 2 | NA18950.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.25+6739G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444440 | ||||||
chr16:66444528
|
C | G | 1 | a0001c0001t0002g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.25+6827C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444528 | ||||||
chr16:66444609
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.25+6908C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444609 | ||||||
chr16:66444834
|
G | T | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+7133G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444834 | ||||||
chr16:66444999
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0262 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+7298G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444999 | ||||||
chr16:66445182
|
A | G | 2 | a0001c0001t0003g0104a0001c0001t0003g0106 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.25+7481A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445182 | ||||||
chr16:66445198
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+7497C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445198 | ||||||
chr16:66445293
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.25+7592G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445293 | ||||||
chr16:66445411
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+7710G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445411 | ||||||
chr16:66445475
|
C | CA | 22 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0133others(19): Show | 22 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.25+7814dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
C | CAA | 7 | a0001c0001t0001g0015a0001c0001t0001g0101a0001c0001t0001g0178others(4): Show | 7 | HG00738.hp2 HG01175.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+7813_25+7814dup others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CA | C | 18 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0053others(15): Show | 18 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+7814delA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAA | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 7 | HG02486.hp2 HG02922.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+7813_25+7814del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAA | C | 7 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0118others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7812_25+7814del others(3): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0001g0014a0001c0001t0002g0120a0001c0001t0002g0121others(4): Show | 7 | HG01433.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7803_25+7814del others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.25+7802_25+7814del others(13): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.25+7800_25+7814del others(15): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(9): Show |
C | 22 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(19): Show | 22 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+7799_25+7814del others(16): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(10): Show |
C | 56 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0043others(53): Show | 59 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.25+7798_25+7814del others(17): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(11): Show |
C | 4 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0085others(1): Show | 4 | HG02004.hp1 NA18747.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+7797_25+7814del others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(12): Show |
C | 6 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0204others(3): Show | 6 | HG01109.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+7796_25+7814del others(19): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(13): Show |
C | 64 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(61): Show | 70 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.25+7795_25+7814del others(20): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(14): Show |
C | 15 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0129others(12): Show | 17 | HG01109.hp2 HG02559.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.25+7794_25+7814del others(21): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445475
|
CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0001g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.25+7793_25+7814del others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | |||||
chr16:66445523
|
G | A | 17 | a0001c0001t0001g0128a0001c0001t0001g0253a0001c0001t0001g0257others(14): Show | 17 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.25+7822G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445523 | ||||||
chr16:66445549
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(181): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.25+7848A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445549 | ||||||
chr16:66445577
|
T | A | 1 | a0001c0001t0004g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.25+7876T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445577 | ||||||
chr16:66445653
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | HG00558.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.25+7952G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445653 | ||||||
chr16:66445749
|
C | G | 1 | a0001c0001t0002g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.25+8048C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445749 | ||||||
chr16:66445759
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(275): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.25+8058G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445759 | ||||||
chr16:66445797
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0043others(74): Show | 80 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.25+8096G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445797 | ||||||
chr16:66445798
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+8097G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445798 | ||||||
chr16:66446052
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.25+8351G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446052 | ||||||
chr16:66446057
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+8356C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446057 | ||||||
chr16:66446098
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+8397G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446098 | ||||||
chr16:66446205
|
A | G | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0164 | 3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.25+8504A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446205 | ||||||
chr16:66446411
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+8710A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446411 | ||||||
chr16:66446412
|
T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+8711T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446412 | ||||||
chr16:66446413
|
A | G | 1 | a0001c0001t0002g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+8712A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446413 | ||||||
chr16:66446526
|
G | A | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(85): Show | 96 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.25+8825G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446526 | ||||||
chr16:66446841
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.25+9140C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446841 | ||||||
chr16:66446898
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+9197C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446898 | ||||||
chr16:66447164
|
G | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+9463G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447164 | ||||||
chr16:66447191
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.25+9490G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447191 | ||||||
chr16:66447198
|
A | G | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0164 | 3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.25+9497A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447198 | ||||||
chr16:66447577
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+9876T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447577 | ||||||
chr16:66447642
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0129a0001c0001t0001g0131others(2): Show | 5 | HG01109.hp2 HG03927.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+9941C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447642 | ||||||
chr16:66447927
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.25+10226A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447927 | ||||||
chr16:66447942
|
A | G | 4 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0164others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+10241A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447942 | ||||||
chr16:66447965
|
A | G | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0164 | 3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.25+10264A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447965 | ||||||
chr16:66448158
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.25+10457C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448158 | ||||||
chr16:66448229
|
T | TTTG | 189 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.25+10537_25+10539d others(5): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66448229 | |||||
chr16:66448260
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0043others(63): Show | 69 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.25+10559C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448260 | ||||||
chr16:66448271
|
A | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0252a0001c0001t0002g0251 | 3 | NA18942.hp2 NA18947.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.25+10570A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448271 | ||||||
chr16:66448363
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.25+10662G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448363 | ||||||
chr16:66448667
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+10966A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448667 | ||||||
chr16:66448690
|
G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+10989G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448690 | ||||||
chr16:66448692
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0059a0001c0001t0002g0061 | 3 | HG01257.hp1 HG01258.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.25+10991G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448692 | ||||||
chr16:66448770
|
C | T | 18 | a0001c0001t0001g0128a0001c0001t0001g0178a0001c0001t0001g0253others(15): Show | 18 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+11069C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448770 | ||||||
chr16:66448804
|
G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+11103G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448804 | ||||||
chr16:66448808
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+11107C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448808 | ||||||
chr16:66449459
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+11758T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449459 | ||||||
chr16:66449483
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(72): Show | 78 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.25+11782T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449483 | ||||||
chr16:66449542
|
T | G | 9 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG02083.hp2 NA18612.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+11841T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449542 | ||||||
chr16:66449606
|
C | CA | 61 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0054others(58): Show | 64 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.25+11926dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | |||||
chr16:66449606
|
C | CAA | 26 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0086others(23): Show | 26 | HG01256.hp2 HG02027.hp2 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.25+11925_25+11926d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | |||||
chr16:66449606
|
C | CAAA | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(84): Show | 95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.25+11924_25+11926d others(5): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | |||||
chr16:66449606
|
C | CAAAA | 7 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0224others(4): Show | 7 | HG00544.hp1 HG01109.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+11923_25+11926d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | |||||
chr16:66449701
|
A | G | 3 | a0001c0001t0003g0134a0001c0001t0003g0142a0001c0001t0003g0147 | 3 | NA18998.hp2 NA19005.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.25+12000A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449701 | ||||||
chr16:66449903
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(90): Show | 100 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.25+12202C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449903 | ||||||
chr16:66449960
|
G | T | 1 | a0001c0001t0003g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.25+12259G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449960 | ||||||
chr16:66450041
|
C | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(62): Show | 68 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.25+12340C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450041 | ||||||
chr16:66450163
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+12462T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450163 | ||||||
chr16:66450219
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.25+12518A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450219 | ||||||
chr16:66450291
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.25+12590C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450291 | ||||||
chr16:66450382
|
T | G | 6 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+12681T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450382 | ||||||
chr16:66450733
|
T | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(183): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.25+13032T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450733 | ||||||
chr16:66450826
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.25+13125G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450826 | ||||||
chr16:66451069
|
C | G | 1 | a0003c0002t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.25+13368C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451069 | ||||||
chr16:66451165
|
A | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(61): Show | 67 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.25+13464A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451165 | ||||||
chr16:66451236
|
C | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+13535C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451236 | ||||||
chr16:66451250
|
C | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+13549C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451250 | ||||||
chr16:66451426
|
A | C | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+13725A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451426 | ||||||
chr16:66451579
|
A | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(173): Show | 187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.25+13878A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451579 | ||||||
chr16:66451590
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(172): Show | 186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.25+13889T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451590 | ||||||
chr16:66451639
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(62): Show | 68 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.25+13938G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451639 | ||||||
chr16:66451685
|
G | A | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+13984G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451685 | ||||||
chr16:66452170
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.25+14469G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452170 | ||||||
chr16:66452236
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.25+14535T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452236 | ||||||
chr16:66452292
|
G | C | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+14591G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452292 | ||||||
chr16:66452671
|
A | G | 47 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0051others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.25+14970A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452671 | ||||||
chr16:66452787
|
CACTT | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0129others(5): Show | 9 | HG01109.hp2 HG02559.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+15089_25+15092d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66452787 | |||||
chr16:66452812
|
G | A | 1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.25+15111G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452812 | ||||||
chr16:66452921
|
C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+15220C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452921 | ||||||
chr16:66452921
|
C | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0274 | 2 | HG00741.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.25+15220C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452921 | ||||||
chr16:66452927
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.25+15226A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452927 | ||||||
chr16:66453022
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0036others(136): Show | 144 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.25+15321A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453022 | ||||||
chr16:66453058
|
A | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+15357A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453058 | ||||||
chr16:66453085
|
G | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(122): Show | 129 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.25+15384G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453085 | ||||||
chr16:66453110
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.25+15409G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453110 | ||||||
chr16:66453158
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0007g0108a0001c0001t0007g0109 | 3 | HG03540.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.25+15457G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453158 | ||||||
chr16:66453303
|
A | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(64): Show | 70 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.25+15602A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453303 | ||||||
chr16:66453342
|
T | TAC | 53 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0051others(50): Show | 54 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.25+15667_25+15668d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | |||||
chr16:66453342
|
T | TACAC | 7 | a0001c0001t0001g0180a0001c0001t0001g0204a0001c0001t0003g0163others(4): Show | 7 | HG01175.hp2 HG01993.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+15665_25+15668d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | |||||
chr16:66453342
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+15657_25+15668d others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | |||||
chr16:66453342
|
TACACAC | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+15663_25+15668d others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | |||||
chr16:66453342
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0003g0114a0001c0001t0003g0154 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.25+15659_25+15668d others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | |||||
chr16:66453731
|
A | AT | 76 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.26-15859dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453731 | |||||
chr16:66453731
|
AT | A | 43 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0051others(40): Show | 44 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.26-15859delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453731 | |||||
chr16:66453743
|
T | G | 2 | a0001c0001t0001g0255a0001c0001t0003g0163 | 2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.26-15859T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453743 | ||||||
chr16:66453824
|
T | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-15778T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453824 | ||||||
chr16:66453939
|
G | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.26-15663G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453939 | ||||||
chr16:66453960
|
C | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(75): Show | 81 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.26-15642C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453960 | ||||||
chr16:66454027
|
G | A | 3 | a0001c0001t0001g0283a0001c0001t0006g0284a0001c0001t0009g0019 | 3 | HG02109.hp2 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.26-15575G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454027 | ||||||
chr16:66454262
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-15340G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454262 | ||||||
chr16:66454649
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-14953T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454649 | ||||||
chr16:66454725
|
C | G | 2 | a0001c0001t0007g0108a0001c0001t0007g0109 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.26-14877C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454725 | ||||||
chr16:66454729
|
C | CT | 32 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0033others(29): Show | 35 | HG00280.hp1 HG00738.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.26-14853dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66454729 | |||||
chr16:66454729
|
CT | C | 38 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0038others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.26-14853delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66454729 | |||||
chr16:66454729
|
CTT | C | 16 | a0001c0001t0001g0046a0001c0001t0001g0110a0001c0001t0001g0111others(13): Show | 16 | HG00558.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-14854_26-14853d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66454729 | |||||
chr16:66454733
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26-14869T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454733 | ||||||
chr16:66455202
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.26-14400G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455202 | ||||||
chr16:66455320
|
A | C | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-14282A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455320 | ||||||
chr16:66455357
|
A | C | 28 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0051others(25): Show | 29 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.26-14245A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455357 | ||||||
chr16:66455416
|
A | T | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-14186A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455416 | ||||||
chr16:66455458
|
T | C | 1 | a0005c0004t0003g0197 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26-14144T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455458 | ||||||
chr16:66455637
|
C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-13965C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455637 | ||||||
chr16:66455671
|
C | T | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0164 | 3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.26-13931C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455671 | ||||||
chr16:66455688
|
C | CT | 44 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(41): Show | 46 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.26-13898dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66455688 | |||||
chr16:66455688
|
CT | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.26-13898delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66455688 | |||||
chr16:66455688
|
CTT | C | 12 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0110others(9): Show | 12 | HG01255.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-13899_26-13898d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66455688 | |||||
chr16:66455842
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0046others(63): Show | 69 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.26-13760A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455842 | ||||||
chr16:66455860
|
T | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-13742T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455860 | ||||||
chr16:66456134
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-13468G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456134 | ||||||
chr16:66456238
|
G | A | 2 | a0001c0001t0006g0284a0001c0001t0012g0105 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.26-13364G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456238 | ||||||
chr16:66456547
|
G | A | 1 | a0006c0008t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.26-13055G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456547 | ||||||
chr16:66456691
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(67): Show | 73 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.26-12911T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456691 | ||||||
chr16:66456707
|
G | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(8): Show | 12 | HG01069.hp2 HG01109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-12895G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456707 | ||||||
chr16:66456739
|
A | C | 46 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0053others(43): Show | 48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-12863A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456739 | ||||||
chr16:66456760
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.26-12842G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456760 | ||||||
chr16:66456790
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(68): Show | 74 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.26-12812G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456790 | ||||||
chr16:66457013
|
C | G | 56 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(53): Show | 57 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.26-12589C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457013 | ||||||
chr16:66457218
|
G | T | 1 | a0001c0001t0002g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.26-12384G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457218 | ||||||
chr16:66457336
|
G | T | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.26-12266G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457336 | ||||||
chr16:66457423
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-12179C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457423 | ||||||
chr16:66457584
|
C | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-12018C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457584 | ||||||
chr16:66457707
|
C | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0249a0001c0001t0004g0012 | 4 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-11895C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457707 | ||||||
chr16:66457785
|
C | CA | 58 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(55): Show | 61 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.26-11805dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66457785 | |||||
chr16:66457785
|
C | CAA | 7 | a0001c0001t0002g0060a0001c0001t0002g0079a0001c0001t0002g0090others(4): Show | 7 | HG00558.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-11806_26-11805d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66457785 | |||||
chr16:66457887
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.26-11715G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457887 | ||||||
chr16:66458027
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.26-11575G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458027 | ||||||
chr16:66458151
|
C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-11451C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458151 | ||||||
chr16:66458175
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-11427T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458175 | ||||||
chr16:66458211
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0159 | 2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.26-11391A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458211 | ||||||
chr16:66458356
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.26-11246G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458356 | ||||||
chr16:66458466
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.26-11136C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458466 | ||||||
chr16:66458502
|
G | A | 2 | a0001c0001t0001g0285a0001c0001t0006g0284 | 2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.26-11100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458502 | ||||||
chr16:66458561
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-11041C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458561 | ||||||
chr16:66458589
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0273 | 2 | HG00323.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.26-11013C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458589 | ||||||
chr16:66458626
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0003g0175a0001c0001t0003g0195 | 3 | HG01256.hp1 HG01258.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.26-10976A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458626 | ||||||
chr16:66458650
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.26-10952T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458650 | ||||||
chr16:66458753
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(76): Show | 83 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-10849G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458753 | ||||||
chr16:66458884
|
G | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-10718G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458884 | ||||||
chr16:66458985
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-10617T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458985 | ||||||
chr16:66459181
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.26-10421A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459181 | ||||||
chr16:66459275
|
C | T | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 59 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.26-10327C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459275 | ||||||
chr16:66459445
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26-10157G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459445 | ||||||
chr16:66459463
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.26-10139G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459463 | ||||||
chr16:66459653
|
C | A | 9 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 9 | HG02486.hp1 HG02896.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-9949C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459653 | ||||||
chr16:66459666
|
G | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-9936G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459666 | ||||||
chr16:66459746
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.26-9856T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459746 | ||||||
chr16:66459836
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.26-9766T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459836 | ||||||
chr16:66460071
|
G | C | 3 | a0001c0001t0001g0283a0001c0001t0007g0108a0001c0001t0007g0109 | 3 | HG02451.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.26-9531G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460071 | ||||||
chr16:66460101
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.26-9501T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460101 | ||||||
chr16:66460120
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.26-9482G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460120 | ||||||
chr16:66460155
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(76): Show | 83 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-9447T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460155 | ||||||
chr16:66460271
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0054others(53): Show | 59 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.26-9331G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460271 | ||||||
chr16:66460428
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0165 | 2 | NA19003.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.26-9174G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460428 | ||||||
chr16:66460501
|
G | A | 47 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0053others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-9101G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460501 | ||||||
chr16:66461192
|
G | A | 1 | a0001c0001t0004g0012 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.26-8410G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461192 | ||||||
chr16:66461309
|
C | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0061 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.26-8293C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461309 | ||||||
chr16:66461314
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.26-8288C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461314 | ||||||
chr16:66461320
|
C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-8282C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461320 | ||||||
chr16:66461321
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.26-8281G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461321 | ||||||
chr16:66461366
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0004g0040 | 2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26-8236G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461366 | ||||||
chr16:66461424
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0025others(135): Show | 143 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.26-8178T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461424 | ||||||
chr16:66461462
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.26-8140C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461462 | ||||||
chr16:66461563
|
G | A | 12 | a0001c0001t0001g0178a0001c0001t0001g0257a0001c0001t0001g0258others(9): Show | 12 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-8039G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461563 | ||||||
chr16:66461569
|
G | GAC | 12 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0023others(9): Show | 13 | HG00323.hp1 HG01109.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-7989_26-7988dup others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
G | GACAC | 55 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0024others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.26-7991_26-7988dup others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
G | GACACAC | 32 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0030others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-7993_26-7988dup others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
G | GACACACA others(1): Show |
6 | a0001c0001t0001g0132a0001c0001t0001g0237a0001c0001t0001g0238others(3): Show | 6 | HG00609.hp2 HG00642.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-7995_26-7988dup others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
G | GACACACA others(3): Show |
11 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0209others(8): Show | 14 | HG00544.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.26-7997_26-7988dup others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
G | GACACACA others(5): Show |
3 | a0001c0001t0001g0240a0001c0001t0003g0175a0001c0001t0003g0195 | 3 | HG01256.hp1 HG01258.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.26-7999_26-7988dup others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
G | GACACACA others(7): Show |
1 | a0001c0001t0002g0251 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.26-8001_26-7988dup others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
G | GACACACA others(9): Show |
1 | a0001c0001t0002g0243 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.26-8003_26-7988dup others(16): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
GAC | G | 20 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0128others(17): Show | 22 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.26-7989_26-7988del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
GACAC | G | 32 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0053others(29): Show | 33 | HG00544.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-7991_26-7988del others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
GACACACA others(1): Show |
G | 5 | a0001c0001t0001g0283a0001c0001t0003g0124a0001c0001t0003g0163others(2): Show | 5 | HG01993.hp1 HG02451.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-7995_26-7988del others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
GACACACA others(3): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.26-7997_26-7988del others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
GACACACA others(5): Show |
G | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0249others(6): Show | 10 | HG01069.hp2 HG01255.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-7999_26-7988del others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
GACACACA others(7): Show |
G | 70 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(67): Show | 73 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.26-8001_26-7988del others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461569
|
GACACACA others(9): Show |
G | 2 | a0001c0001t0004g0004a0001c0001t0009g0019 | 3 | HG00738.hp1 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.26-8003_26-7988del others(16): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | |||||
chr16:66461613
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.26-7988_26-7987ins others(11): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461613 | |||||
chr16:66461615
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.26-7987A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461615 | ||||||
chr16:66461742
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26-7860G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461742 | ||||||
chr16:66461765
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0005g0231 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.26-7837T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461765 | ||||||
chr16:66461778
|
A | C | 16 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0001t0001g0111others(13): Show | 17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-7824A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461778 | ||||||
chr16:66461808
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-7794T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461808 | ||||||
chr16:66461885
|
C | T | 1 | a0001c0001t0003g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.26-7717C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461885 | ||||||
chr16:66461975
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26-7627C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461975 | ||||||
chr16:66462018
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.26-7584T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462018 | ||||||
chr16:66462158
|
C | T | 47 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0053others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-7444C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462158 | ||||||
chr16:66462196
|
C | T | 16 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0001t0001g0111others(13): Show | 17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-7406C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462196 | ||||||
chr16:66462444
|
T | C | 1 | a0006c0008t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.26-7158T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462444 | ||||||
chr16:66462572
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0249a0001c0001t0004g0012 | 4 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-7030C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462572 | ||||||
chr16:66462573
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0003g0256 | 2 | HG04204.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.26-7029G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462573 | ||||||
chr16:66462658
|
G | T | 1 | a0001c0001t0004g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.26-6944G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462658 | ||||||
chr16:66462687
|
G | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0054others(74): Show | 81 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.26-6915G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462687 | ||||||
chr16:66462731
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG01071.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.26-6871G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462731 | ||||||
chr16:66462755
|
C | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0186a0001c0001t0001g0249others(1): Show | 5 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-6847C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462755 | ||||||
chr16:66462984
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0025others(136): Show | 144 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.26-6618A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462984 | ||||||
chr16:66463113
|
A | T | 1 | a0001c0001t0003g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.26-6489A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463113 | ||||||
chr16:66463114
|
C | G | 1 | a0001c0001t0003g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.26-6488C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463114 | ||||||
chr16:66463410
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.26-6192T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463410 | ||||||
chr16:66463510
|
G | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-6092G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463510 | ||||||
chr16:66463591
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-6011G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463591 | ||||||
chr16:66463762
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.26-5840G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463762 | ||||||
chr16:66463947
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.26-5655G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463947 | ||||||
chr16:66464037
|
G | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0054others(57): Show | 63 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-5565G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464037 | ||||||
chr16:66464126
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(59): Show | 65 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.26-5476A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464126 | ||||||
chr16:66464156
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.26-5446C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464156 | ||||||
chr16:66464225
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.26-5377T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464225 | ||||||
chr16:66464399
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.26-5203T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464399 | ||||||
chr16:66464590
|
G | A | 16 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0001t0001g0111others(13): Show | 17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-5012G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464590 | ||||||
chr16:66464630
|
A | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0249 | 2 | HG01069.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.26-4972A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464630 | ||||||
chr16:66464771
|
T | C | 2 | a0001c0001t0001g0036a0006c0008t0001g0050 | 2 | HG00609.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.26-4831T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464771 | ||||||
chr16:66464821
|
T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-4781T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464821 | ||||||
chr16:66464925
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0233a0001c0001t0001g0235 | 3 | HG02683.hp1 HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.26-4677G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464925 | ||||||
chr16:66464997
|
G | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0054others(48): Show | 54 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.26-4605G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464997 | ||||||
chr16:66465231
|
G | A | 16 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0001t0001g0111others(13): Show | 17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-4371G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465231 | ||||||
chr16:66465319
|
C | T | 2 | a0002c0003t0002g0080a0002c0003t0002g0158 | 2 | NA19007.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-4283C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465319 | ||||||
chr16:66465456
|
T | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-4146T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465456 | ||||||
chr16:66465508
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0054others(76): Show | 83 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-4094G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465508 | ||||||
chr16:66465577
|
G | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-4025G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465577 | ||||||
chr16:66465672
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.26-3930T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465672 | ||||||
chr16:66465722
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(77): Show | 84 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-3880C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465722 | ||||||
chr16:66465975
|
GCTAA | G | 3 | a0001c0001t0001g0283a0001c0001t0007g0108a0001c0001t0007g0109 | 3 | HG02451.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.26-3624_26-3621del others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66465975 | |||||
chr16:66466066
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-3536G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466066 | ||||||
chr16:66466104
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0230 | 4 | HG00323.hp1 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-3498G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466104 | ||||||
chr16:66466109
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-3493C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466109 | ||||||
chr16:66466263
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.26-3339C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466263 | ||||||
chr16:66466294
|
A | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-3308A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466294 | ||||||
chr16:66466309
|
C | A | 1 | a0001c0001t0002g0211 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.26-3293C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466309 | ||||||
chr16:66466398
|
TTC | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.26-3198_26-3197del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66466398 | |||||
chr16:66466600
|
T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-3002T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466600 | ||||||
chr16:66466781
|
C | T | 16 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0001t0001g0111others(13): Show | 17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-2821C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466781 | ||||||
chr16:66467045
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0249 | 2 | HG01069.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.26-2557T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467045 | ||||||
chr16:66467307
|
A | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0043others(58): Show | 64 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.26-2295A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467307 | ||||||
chr16:66467335
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.26-2267C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467335 | ||||||
chr16:66467362
|
C | T | 1 | a0001c0001t0003g0142 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.26-2240C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467362 | ||||||
chr16:66467389
|
G | A | 1 | a0001c0001t0003g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.26-2213G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467389 | ||||||
chr16:66467390
|
G | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-2212G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467390 | ||||||
chr16:66467442
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.26-2160C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467442 | ||||||
chr16:66467515
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-2087C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467515 | ||||||
chr16:66467555
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-2047C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467555 | ||||||
chr16:66467593
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(45): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.26-2009G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467593 | ||||||
chr16:66467731
|
G | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1871G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467731 | ||||||
chr16:66467816
|
G | A | 13 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(10): Show | 13 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-1786G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467816 | ||||||
chr16:66467877
|
C | A | 1 | a0001c0001t0001g0212 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.26-1725C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467877 | ||||||
chr16:66468109
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.26-1493G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468109 | ||||||
chr16:66468234
|
T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1368T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468234 | ||||||
chr16:66468257
|
A | C | 7 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005others(4): Show | 10 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-1345A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468257 | ||||||
chr16:66468257
|
A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1345A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468257 | ||||||
chr16:66468354
|
G | C | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG01071.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.26-1248G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468354 | ||||||
chr16:66468478
|
C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-1124C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468478 | ||||||
chr16:66468515
|
A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1087A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468515 | ||||||
chr16:66468576
|
C | T | 5 | a0001c0001t0002g0115a0001c0001t0002g0117a0001c0001t0002g0121others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-1026C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468576 | ||||||
chr16:66468585
|
G | T | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1017G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468585 | ||||||
chr16:66468588
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-1014G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468588 | ||||||
chr16:66468605
|
C | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-997C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468605 | ||||||
chr16:66468674
|
A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-928A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468674 | ||||||
chr16:66468730
|
C | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-872C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468730 | ||||||
chr16:66468873
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-729C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468873 | ||||||
chr16:66468893
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.26-709A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468893 | ||||||
chr16:66468946
|
A | C | 1 | a0001c0001t0003g0147 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.26-656A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468946 | ||||||
chr16:66469101
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.26-501A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469101 | ||||||
chr16:66469148
|
C | T | 47 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0053others(44): Show | 48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-454C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469148 | ||||||
chr16:66469270
|
C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-332C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469270 | ||||||
chr16:66469362
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-240C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469362 | ||||||
chr16:66469477
|
G | A | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-125G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469477 | ||||||
chr16:66469536
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26-66G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469536 | ||||||
chr16:66469875
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+10C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66469875 | ||||||
chr16:66469972
|
G | A | 12 | a0001c0001t0001g0178a0001c0001t0001g0257a0001c0001t0001g0258others(9): Show | 12 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.289+107G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66469972 | ||||||
chr16:66469979
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289+114C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66469979 | ||||||
chr16:66470170
|
C | CGATG | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(67): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.289+351_289+354dup others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | |||||
chr16:66470170
|
C | CGATGGAT others(1): Show |
7 | a0001c0001t0001g0030a0001c0001t0001g0107a0001c0001t0001g0178others(4): Show | 7 | HG02004.hp2 HG02809.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+347_289+354dup others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | |||||
chr16:66470170
|
C | CGATGGAT others(5): Show |
1 | a0001c0001t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.289+343_289+354dup others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | |||||
chr16:66470170
|
CGATG | C | 13 | a0001c0001t0001g0096a0001c0001t0001g0173a0001c0001t0001g0249others(10): Show | 16 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.289+351_289+354del others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | |||||
chr16:66470170
|
CGATGGAT others(1): Show |
C | 12 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(9): Show | 12 | HG01109.hp2 HG01175.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+347_289+354del others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | |||||
chr16:66470170
|
CGATGGAT others(5): Show |
C | 45 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0053others(42): Show | 46 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.289+343_289+354del others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | |||||
chr16:66470870
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289+1005T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66470870 | ||||||
chr16:66470989
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.289+1124C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66470989 | ||||||
chr16:66471435
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0025others(138): Show | 146 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.289+1570A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471435 | ||||||
chr16:66471440
|
G | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.289+1575G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471440 | ||||||
chr16:66471464
|
G | A | 2 | a0001c0001t0001g0285a0001c0001t0009g0019 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.289+1599G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471464 | ||||||
chr16:66471549
|
T | G | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.289+1684T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471549 | ||||||
chr16:66471666
|
A | G | 2 | a0001c0001t0006g0284a0001c0001t0009g0019 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.289+1801A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471666 | ||||||
chr16:66471676
|
T | C | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.289+1811T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471676 | ||||||
chr16:66471812
|
A | G | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(8): Show | 11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+1947A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471812 | ||||||
chr16:66471816
|
C | T | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289+1951C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471816 | ||||||
chr16:66471911
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.289+2046G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471911 | ||||||
chr16:66472124
|
C | A | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.289+2259C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472124 | ||||||
chr16:66472346
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.289+2481A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472346 | ||||||
chr16:66472478
|
C | T | 2 | a0001c0001t0003g0114a0001c0001t0003g0154 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.289+2613C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472478 | ||||||
chr16:66472755
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0249a0001c0001t0004g0012 | 4 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+2890C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472755 | ||||||
chr16:66472786
|
A | G | 66 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0043others(63): Show | 68 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.289+2921A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472786 | ||||||
chr16:66472875
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.289+3010A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472875 | ||||||
chr16:66472886
|
A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.289+3021A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472886 | ||||||
chr16:66472948
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289+3083G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472948 | ||||||
chr16:66473039
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289+3174T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473039 | ||||||
chr16:66473173
|
T | C | 126 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(123): Show | 130 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.289+3308T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473173 | ||||||
chr16:66473207
|
G | A | 48 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0053others(45): Show | 50 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.289+3342G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473207 | ||||||
chr16:66473311
|
C | G | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.289+3446C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473311 | ||||||
chr16:66473346
|
G | T | 1 | a0001c0001t0003g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.289+3481G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473346 | ||||||
chr16:66473382
|
C | T | 2 | a0001c0001t0003g0160a0001c0001t0003g0161 | 2 | NA19012.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.289+3517C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473382 | ||||||
chr16:66473505
|
G | A | 4 | a0001c0001t0002g0044a0001c0001t0002g0045a0002c0003t0002g0080others(1): Show | 4 | NA18953.hp1 NA19007.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+3640G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473505 | ||||||
chr16:66473511
|
C | T | 11 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+3646C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473511 | ||||||
chr16:66473551
|
A | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0026others(10): Show | 14 | HG00323.hp1 HG00733.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.289+3686A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473551 | ||||||
chr16:66473556
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0004g0040 | 2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.289+3691G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473556 | ||||||
chr16:66473696
|
CTAAATAA others(9): Show |
C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289+3843_290-3837d others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66473696 | |||||
chr16:66473720
|
A | T | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG01169.hp2 HG01934.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.290-3840A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473720 | ||||||
chr16:66473721
|
T | A | 10 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG01169.hp2 HG01934.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.290-3839T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473721 | ||||||
chr16:66473869
|
G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-3691G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473869 | ||||||
chr16:66474070
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.290-3490C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474070 | ||||||
chr16:66474322
|
T | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290-3238T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474322 | ||||||
chr16:66474443
|
T | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-3117T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474443 | ||||||
chr16:66474544
|
A | AAGAGGGA others(5): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0222a0001c0001t0001g0240 | 3 | NA18969.hp1 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.290-2979_290-2968d others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | |||||
chr16:66474544
|
A | AAGAGGGA others(17): Show |
2 | a0001c0001t0001g0202a0001c0001t0001g0236 | 2 | HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.290-2991_290-2968d others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | |||||
chr16:66474544
|
A | AAGAGGGA others(81): Show |
1 | a0001c0001t0004g0012 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.290-2992_290-2991i others(90): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | |||||
chr16:66474544
|
A | AAGAGGGA others(85): Show |
1 | a0001c0001t0002g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(94): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | |||||
chr16:66474544
|
A | AAGAGGGA others(25): Show |
1 | a0001c0001t0002g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.290-3004_290-3003i others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | |||||
chr16:66474544
|
AAGAGGGA others(53): Show |
A | 1 | a0001c0001t0002g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.290-3003_290-2944d others(62): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | |||||
chr16:66474545
|
A | AGAGGGAG others(17): Show |
1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.290-2992_290-2991i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474545 | |||||
chr16:66474557
|
A | AGAGGGAG others(1): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0129others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-2999_290-2992d others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | |||||
chr16:66474557
|
A | AGAGGGAG others(29): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0201 | 2 | NA18953.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.290-2979_290-2944d others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | |||||
chr16:66474557
|
A | AGAGGGAG others(5): Show |
1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | |||||
chr16:66474557
|
A | AGAGGGAG others(9): Show |
1 | a0001c0001t0001g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | |||||
chr16:66474557
|
A | AGAGGGAG others(65): Show |
1 | a0001c0001t0001g0208 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(74): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | |||||
chr16:66474561
|
G | GGAGGGAG others(9): Show |
1 | a0001c0001t0001g0025 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474561 | |||||
chr16:66474562
|
G | GAGGGAGA others(25): Show |
1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.290-2984_290-2983i others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474562 | |||||
chr16:66474569
|
A | AGAGGGAG others(13): Show |
1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-2979_290-2960d others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(45): Show |
1 | a0001c0005t0001g0200 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.290-2968_290-2967i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(25): Show |
3 | a0001c0001t0001g0178a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG00642.hp2 HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.290-2987_290-2956d others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(77): Show |
1 | a0001c0001t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.290-2910_290-2909i others(86): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(5): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0168 | 2 | HG03927.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.290-2980_290-2979i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(453): Show |
1 | a0001c0001t0001g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.290-2980_290-2979i others(462): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(77): Show |
1 | a0001c0001t0001g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290-2980_290-2979i others(86): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(165): Show |
2 | a0001c0001t0001g0033a0001c0001t0004g0040 | 2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290-2980_290-2979i others(174): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | AGAGGGAG others(45): Show |
1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.290-2980_290-2979i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474569
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0110others(14): Show | 17 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.290-2991A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474569 | ||||||
chr16:66474569
|
AGAGG | A | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.290-2983_290-2980d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | |||||
chr16:66474570
|
G | GAGGGAGG others(29): Show |
1 | a0001c0001t0007g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-2980_290-2979i others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474570 | |||||
chr16:66474573
|
GGAGGGAG others(1): Show |
G | 12 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0095others(9): Show | 13 | HG00621.hp2 HG00673.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-2979_290-2972d others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474573 | |||||
chr16:66474574
|
G | GAGGGAGG others(17): Show |
1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.290-2980_290-2979i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474574 | |||||
chr16:66474577
|
GGAGA | G | 6 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005others(3): Show | 9 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2979_290-2976d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474577 | |||||
chr16:66474577
|
GGAGAGAG others(21): Show |
G | 1 | a0001c0001t0001g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.290-2979_290-2952d others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474577 | |||||
chr16:66474581
|
A | AGAGGGAG others(34): Show |
1 | a0001c0001t0001g0191 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.290-2968_290-2967i others(43): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474581 | |||||
chr16:66474581
|
A | AGAGGGAG others(217): Show |
1 | a0001c0001t0005g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.290-2968_290-2967i others(226): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474581 | |||||
chr16:66474581
|
A | AGAGGGAG others(5): Show |
1 | a0001c0001t0001g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.290-2967_290-2956d others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474581 | |||||
chr16:66474581
|
A | G | 21 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(18): Show | 21 | HG00609.hp1 HG00621.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.290-2979A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474581 | ||||||
chr16:66474589
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.290-2971G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474589 | ||||||
chr16:66474590
|
G | A | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.290-2970G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474590 | ||||||
chr16:66474590
|
G | GAGGA | 6 | a0001c0001t0001g0053a0001c0001t0003g0114a0001c0001t0003g0141others(3): Show | 6 | HG00621.hp1 HG02015.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-2967_290-2966i others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474590 | |||||
chr16:66474593
|
G | A | 46 | a0001c0001t0001g0010a0001c0001t0001g0051a0001c0001t0001g0062others(43): Show | 48 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.290-2967G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474593 | ||||||
chr16:66474594
|
G | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0252a0001c0001t0003g0114others(6): Show | 9 | HG00621.hp1 HG02015.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2966G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474594 | ||||||
chr16:66474598
|
G | A | 10 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0002g0039others(7): Show | 13 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-2962G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474598 | ||||||
chr16:66474601
|
G | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0167others(6): Show | 10 | HG00621.hp2 HG00673.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-2959G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474601 | ||||||
chr16:66474601
|
GGAGA | G | 6 | a0001c0001t0003g0137a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG00733.hp1 HG01099.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2955_290-2952d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474601 | |||||
chr16:66474602
|
G | A | 20 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0053others(17): Show | 23 | HG00621.hp1 HG00738.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.290-2958G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474602 | ||||||
chr16:66474602
|
G | GAGGAAGG others(1): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0217a0001c0001t0004g0041others(1): Show | 4 | HG02145.hp2 HG03041.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2956_290-2955i others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474602 | |||||
chr16:66474602
|
G | GAGGAAGG others(9): Show |
5 | a0001c0001t0003g0007a0001c0001t0003g0142a0001c0001t0003g0147others(2): Show | 6 | NA18950.hp1 NA18968.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2956_290-2955i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474602 | |||||
chr16:66474602
|
G | GAGGAAGG others(89): Show |
1 | a0001c0001t0001g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290-2956_290-2955i others(98): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474602 | |||||
chr16:66474603
|
A | AGGAAGGA others(3): Show |
4 | a0001c0001t0003g0123a0001c0001t0003g0150a0001c0001t0003g0177others(1): Show | 4 | HG02723.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2956_290-2955i others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474603 | |||||
chr16:66474605
|
A | AGAGGGAG others(117): Show |
1 | a0001c0001t0003g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(126): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474605 | |||||
chr16:66474605
|
A | AGAGGGAG others(9): Show |
1 | a0001c0001t0003g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474605 | |||||
chr16:66474605
|
A | G | 93 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0025others(90): Show | 100 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.290-2955A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474605 | ||||||
chr16:66474606
|
G | A | 19 | a0001c0001t0001g0031a0001c0001t0001g0129a0001c0001t0001g0208others(16): Show | 20 | HG00609.hp1 HG02257.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-2954G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474606 | ||||||
chr16:66474606
|
G | GAGGGAGG others(29): Show |
1 | a0001c0001t0003g0250 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.290-2943_290-2942i others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474606 | |||||
chr16:66474606
|
G | GAGGGAGG others(121): Show |
1 | a0001c0001t0001g0034 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(130): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474606 | |||||
chr16:66474606
|
G | GGA | 4 | a0001c0001t0003g0123a0001c0001t0003g0150a0001c0001t0003g0177others(1): Show | 4 | HG02723.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2954_290-2953i others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474606 | ||||||
chr16:66474610
|
G | A | 37 | a0001c0001t0001g0025a0001c0001t0001g0118a0001c0001t0001g0119others(34): Show | 41 | HG00609.hp1 HG00733.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.290-2950G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474610 | ||||||
chr16:66474610
|
G | GAGGGAGA others(141): Show |
1 | a0001c0001t0002g0279 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(150): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | |||||
chr16:66474610
|
G | GAGGGAGA others(129): Show |
1 | a0001c0001t0002g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(138): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | |||||
chr16:66474610
|
G | GAGGGAGA others(149): Show |
1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(158): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | |||||
chr16:66474610
|
G | GAGGGAGA others(33): Show |
1 | a0001c0001t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(42): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | |||||
chr16:66474610
|
G | GAGGGAGG others(13): Show |
1 | a0001c0001t0002g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | |||||
chr16:66474610
|
G | GAGGGAGG others(21): Show |
1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.290-2943_290-2942i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | |||||
chr16:66474614
|
G | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0031others(15): Show | 19 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.290-2946G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474614 | ||||||
chr16:66474614
|
G | GAGAGAGG others(141): Show |
1 | a0001c0001t0002g0003 | 2 | HG01975.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.290-2944_290-2943i others(150): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGAGAGG others(57): Show |
1 | a0001c0001t0001g0274 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(66): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGAGAGG others(49): Show |
1 | a0001c0001t0003g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(58): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGAGAGG others(37): Show |
1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(46): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGAGAGG others(101): Show |
1 | a0001c0001t0001g0257 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(110): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGAGAGG others(33): Show |
6 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0173others(3): Show | 6 | HG00408.hp2 HG02083.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2944_290-2943i others(42): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGAGAGG others(33): Show |
1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(42): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGGGAGG others(105): Show |
1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(114): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGGGAGG others(21): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0001g0096others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2943_290-2942i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGGGAGG others(117): Show |
5 | a0001c0001t0002g0115a0001c0001t0002g0117a0001c0001t0002g0121others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-2943_290-2942i others(126): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474614
|
G | GAGGGAGG others(141): Show |
1 | a0001c0001t0001g0249 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(150): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | |||||
chr16:66474616
|
G | GAGGAGGG others(254): Show |
1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(263): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474616 | ||||||
chr16:66474616
|
G | GGGAGGGA others(169): Show |
2 | a0001c0001t0003g0104a0001c0001t0003g0106 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.290-2943_290-2942i others(178): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474616 | |||||
chr16:66474618
|
A | AAGGAAGG others(9): Show |
3 | a0001c0001t0001g0101a0001c0001t0001g0186a0001c0001t0002g0099 | 3 | HG03669.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.290-2939_290-2938i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGAAGG others(13): Show |
4 | a0001c0001t0001g0131a0001c0001t0001g0180a0001c0001t0003g0155others(1): Show | 4 | HG01169.hp1 HG02602.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2939_290-2938i others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGAAGG others(17): Show |
2 | a0001c0001t0001g0051a0001c0001t0008g0006 | 3 | HG03209.hp1 HG03453.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.290-2939_290-2938i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGAAGG others(25): Show |
1 | a0001c0001t0003g0163 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.290-2939_290-2938i others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGG | 101 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(98): Show | 105 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.290-2913_290-2910d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(1): Show |
9 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(6): Show | 9 | HG00140.hp1 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2917_290-2910d others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(5): Show |
3 | a0001c0001t0003g0176a0001c0001t0003g0198a0001c0001t0003g0199 | 3 | HG02896.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.290-2933_290-2932i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(189): Show |
1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.290-2920_290-2919i others(198): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(109): Show |
1 | a0001c0001t0001g0085 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.290-2920_290-2919i others(118): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(25): Show |
1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.290-2941_290-2910d others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(45): Show |
2 | a0001c0001t0001g0174a0001c0001t0001g0248 | 2 | HG02258.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.290-2910_290-2909i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(45): Show |
1 | a0006c0008t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.290-2910_290-2909i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(137): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0254 | 2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.290-2910_290-2909i others(146): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(45): Show |
2 | a0003c0002t0001g0089a0003c0002t0001g0188 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.290-2910_290-2909i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | AAGGGAGG others(85): Show |
4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0136others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2910_290-2909i others(94): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | |||||
chr16:66474618
|
A | G | 117 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(114): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.290-2942A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474618 | ||||||
chr16:66474621
|
G | GGAGGGAG others(169): Show |
1 | a0001c0001t0002g0211 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.290-2920_290-2919i others(178): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474621 | |||||
chr16:66474621
|
G | GGAGGGAG others(85): Show |
1 | a0001c0001t0001g0170 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.290-2910_290-2909i others(94): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474621 | |||||
chr16:66474622
|
G | A | 8 | a0001c0001t0001g0101a0001c0001t0002g0003a0001c0001t0002g0060others(5): Show | 9 | HG01975.hp1 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2938G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474622 | ||||||
chr16:66474622
|
G | GAGGA | 4 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0002g0097others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2935_290-2934i others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474622
|
G | GAGGAAGG others(17): Show |
14 | a0001c0001t0001g0157a0001c0001t0002g0018a0001c0001t0002g0045others(11): Show | 14 | HG00280.hp2 HG00544.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-2935_290-2934i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474622
|
G | GAGGAAGG others(77): Show |
1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.290-2935_290-2934i others(86): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474622
|
G | GAGGAAGG others(5): Show |
1 | a0001c0001t0002g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.290-2935_290-2934i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474622
|
G | GAGGAAGG others(45): Show |
1 | a0001c0001t0002g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.290-2935_290-2934i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474622
|
G | GAGGAGGA others(19): Show |
1 | a0001c0001t0002g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.290-2935_290-2934i others(28): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474622
|
G | GAGGGAGG others(21): Show |
1 | a0001c0001t0002g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.290-2931_290-2930i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474622
|
G | GAGGGAGG others(29): Show |
4 | a0001c0001t0002g0090a0001c0001t0002g0091a0002c0003t0002g0080others(1): Show | 4 | HG00558.hp1 HG03831.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2923_290-2922i others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | |||||
chr16:66474626
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.290-2934G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474626 | ||||||
chr16:66474629
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0201 | 2 | NA18953.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.290-2931G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474629 | ||||||
chr16:66474637
|
G | GGAGGGAG others(21): Show |
3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG01071.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.290-2910_290-2909i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474637 | |||||
chr16:66474638
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2922G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474638 | ||||||
chr16:66474639
|
A | G | 1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2921A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474639 | ||||||
chr16:66474691
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.290-2869G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474691 | ||||||
chr16:66474730
|
AAAAGAAA others(8): Show |
A | 2 | a0001c0001t0001g0221a0001c0001t0001g0239 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.290-2821_290-2807d others(17): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474730 | |||||
chr16:66474743
|
GAGAA | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0009g0019others(1): Show | 4 | HG02071.hp2 HG02074.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2800_290-2797d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474743 | |||||
chr16:66474918
|
G | A | 1 | a0005c0004t0003g0197 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.290-2642G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474918 | ||||||
chr16:66474965
|
A | T | 1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2595A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474965 | ||||||
chr16:66475056
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0003g0278 | 2 | NA18963.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.290-2504G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475056 | ||||||
chr16:66475079
|
G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-2481G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475079 | ||||||
chr16:66475167
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.290-2393C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475167 | ||||||
chr16:66475222
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(275): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.290-2338A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475222 | ||||||
chr16:66475371
|
C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.290-2189C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475371 | ||||||
chr16:66475748
|
A | G | 7 | a0001c0001t0002g0003a0001c0001t0002g0047a0001c0001t0002g0068others(4): Show | 8 | HG01975.hp1 HG02071.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-1812A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475748 | ||||||
chr16:66475784
|
T | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0227 | 2 | NA18955.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.290-1776T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475784 | ||||||
chr16:66475937
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.290-1623G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475937 | ||||||
chr16:66476042
|
G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-1518G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476042 | ||||||
chr16:66476109
|
CA | C | 60 | a0001c0001t0001g0113a0001c0001t0001g0236a0001c0001t0002g0003others(57): Show | 66 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.290-1436delA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66476109 | |||||
chr16:66476121
|
A | G | 11 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005others(8): Show | 15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.290-1439A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476121 | ||||||
chr16:66476250
|
G | A | 59 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0018others(56): Show | 65 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.290-1310G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476250 | ||||||
chr16:66476275
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-1285G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476275 | ||||||
chr16:66476445
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1115G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476445 | ||||||
chr16:66476447
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1113A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476447 | ||||||
chr16:66476448
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1112A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476448 | ||||||
chr16:66476450
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1110T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476450 | ||||||
chr16:66476451
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1109G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476451 | ||||||
chr16:66476456
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1104A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476456 | ||||||
chr16:66476458
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1102T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476458 | ||||||
chr16:66476460
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1100A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476460 | ||||||
chr16:66476462
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1098A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476462 | ||||||
chr16:66476465
|
A | G | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-1095A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476465 | ||||||
chr16:66476466
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1094G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476466 | ||||||
chr16:66476467
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1093A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476467 | ||||||
chr16:66476468
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1092G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476468 | ||||||
chr16:66476469
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1091A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476469 | ||||||
chr16:66476470
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1090A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476470 | ||||||
chr16:66476471
|
A | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1089A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476471 | ||||||
chr16:66476472
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1088G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476472 | ||||||
chr16:66476473
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1087G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476473 | ||||||
chr16:66476477
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1083T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476477 | ||||||
chr16:66476478
|
A | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1082A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476478 | ||||||
chr16:66476479
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1081G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476479 | ||||||
chr16:66476481
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1079T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476481 | ||||||
chr16:66476483
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1077C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476483 | ||||||
chr16:66476484
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1076G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476484 | ||||||
chr16:66476492
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1068T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476492 | ||||||
chr16:66476493
|
G | A | 2 | a0001c0001t0006g0284a0001c0001t0012g0105 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.290-1067G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476493 | ||||||
chr16:66476498
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1062G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476498 | ||||||
chr16:66476503
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1057A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476503 | ||||||
chr16:66476504
|
C | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1056C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476504 | ||||||
chr16:66476509
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1051A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476509 | ||||||
chr16:66476511
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1049A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476511 | ||||||
chr16:66476512
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1048G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476512 | ||||||
chr16:66476513
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1047G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476513 | ||||||
chr16:66476514
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1046G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476514 | ||||||
chr16:66476515
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1045G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476515 | ||||||
chr16:66476516
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1044A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476516 | ||||||
chr16:66476517
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1043G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476517 | ||||||
chr16:66476518
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1042G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476518 | ||||||
chr16:66476519
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1041A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476519 | ||||||
chr16:66476520
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1040G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476520 | ||||||
chr16:66476521
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1039G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476521 | ||||||
chr16:66476523
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1037A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476523 | ||||||
chr16:66476526
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1034T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476526 | ||||||
chr16:66476527
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1033G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476527 | ||||||
chr16:66476529
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1031G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476529 | ||||||
chr16:66476530
|
A | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1030A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476530 | ||||||
chr16:66476531
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1029G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476531 | ||||||
chr16:66476535
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1025T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476535 | ||||||
chr16:66476536
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1024G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476536 | ||||||
chr16:66476537
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1023G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476537 | ||||||
chr16:66476543
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1017G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476543 | ||||||
chr16:66476551
|
C | G | 1 | a0001c0001t0002g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.290-1009C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476551 | ||||||
chr16:66476878
|
T | TA | 12 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0086others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.290-676dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66476878 | |||||
chr16:66476926
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.290-634T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476926 | ||||||
chr16:66477126
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.290-434C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477126 | ||||||
chr16:66477142
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.290-418C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477142 | ||||||
chr16:66477186
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.290-374C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477186 | ||||||
chr16:66477281
|
G | A | 3 | a0001c0001t0001g0259a0001c0001t0003g0153a0001c0001t0003g0278 | 3 | HG00323.hp2 NA18963.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.290-279G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477281 | ||||||
chr16:66477420
|
G | C | 11 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005others(8): Show | 15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.290-140G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477420 | ||||||
chr16:66477460
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290-100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477460 | ||||||
chr16:66477532
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.290-28G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477532 | ||||||
chr16:66477724
|
A | G | 119 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(116): Show | 127 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.440+14A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66477724 | ||||||
chr16:66477810
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.440+100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66477810 | ||||||
chr16:66478002
|
C | T | 2 | a0001c0001t0003g0155a0001c0007t0003g0245 | 2 | HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.440+292C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478002 | ||||||
chr16:66478158
|
C | G | 1 | a0001c0001t0004g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.440+448C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478158 | ||||||
chr16:66478193
|
T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.440+483T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478193 | ||||||
chr16:66478271
|
G | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.440+561G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478271 | ||||||
chr16:66478385
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.440+675G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478385 | ||||||
chr16:66478387
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.440+677G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478387 | ||||||
chr16:66478443
|
A | G | 11 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005others(8): Show | 15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.440+733A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478443 | ||||||
chr16:66478589
|
G | A | 11 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005others(8): Show | 15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.440+879G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478589 | ||||||
chr16:66478801
|
G | A | 57 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(54): Show | 59 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.440+1091G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478801 | ||||||
chr16:66478832
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0239 | 2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.440+1122C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478832 | ||||||
chr16:66478906
|
G | A | 11 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0005others(8): Show | 15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.440+1196G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478906 | ||||||
chr16:66478921
|
G | A | 57 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0018others(54): Show | 63 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.440+1211G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478921 | ||||||
chr16:66479094
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.440+1384A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479094 | ||||||
chr16:66479166
|
T | G | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1420T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479166 | ||||||
chr16:66479168
|
G | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1418G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479168 | ||||||
chr16:66479169
|
C | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1417C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479169 | ||||||
chr16:66479207
|
A | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.441-1379A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479207 | ||||||
chr16:66479387
|
G | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1199G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479387 | ||||||
chr16:66479601
|
G | C | 1 | a0001c0001t0001g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441-985G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479601 | ||||||
chr16:66479675
|
T | G | 2 | a0001c0001t0009g0019a0001c0001t0012g0105 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.441-911T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479675 | ||||||
chr16:66479738
|
G | C | 1 | a0001c0001t0003g0150 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.441-848G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479738 | ||||||
chr16:66479799
|
G | C | 1 | a0001c0001t0001g0212 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.441-787G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479799 | ||||||
chr16:66479942
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | NA18963.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.441-644C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479942 | ||||||
chr16:66479972
|
G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.441-614G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479972 | ||||||
chr16:66480071
|
AC | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0204 | 3 | HG02109.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.441-511delC | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 66480071 | |||||
chr16:66480146
|
T | A | 9 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.441-440T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66480146 | ||||||
chr16:66480205
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.441-381G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66480205 |