geneid | 80127 |
---|---|
ensemblid | ENSG00000119636.16 |
hgncid | 19855 |
symbol | BBOF1 |
name | basal body orientation factor 1 |
refseq_nuc | NM_025057.3 |
refseq_prot | NP_079333.2 |
ensembl_nuc | ENST00000394009.5 |
ensembl_prot | ENSP00000377577.3 |
mane_status | MANE Select |
chr | chr14 |
start | 74019349 |
end | 74066092 |
strand | + |
ver | v1.2 |
region | chr14:74019349-74066092 |
region5000 | chr14:74014349-74071092 |
regionname0 | BBOF1_chr14_74019349_74066092 |
regionname5000 | BBOF1_chr14_74014349_74071092 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0001 | 0/0 | 529 | 111 | 18 | 16 | 53 | 3 | 21 | 41 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0002 | 1/0 | 529 | 103 | 37 | 23 | 27 | 8 | 7 | 21 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0003 | 0/1 | 529 | 80 | 3 | 9 | 63 | 1 | 3 | 50 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0004 | 0/0 | 529 | 56 | 9 | 22 | 15 | 2 | 8 | 11 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0005 | 0/0 | 529 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0006 | 0/0 | 529 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0007 | 0/0 | 529 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0008 | 0/0 | 529 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0009 | 0/0 | 529 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0010 | 0/0 | 529 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0011 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0012 | 0/0 | 529 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0013 | 0/0 | 529 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0014 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1590 | 111 | 18 | 16 | 53 | 3 | 21 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0002 | 1/0 | 1590 | 102 | 37 | 22 | 27 | 8 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0003 | 0/1 | 1590 | 79 | 3 | 9 | 62 | 1 | 3 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0004 | 0/0 | 1590 | 46 | 0 | 22 | 15 | 2 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0005 | 0/0 | 1590 | 11 | 11 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0006 | 0/0 | 1590 | 11 | 9 | 2 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0007 | 0/0 | 1590 | 7 | 7 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0008 | 0/0 | 1590 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0009 | 0/0 | 1590 | 3 | 2 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0010 | 0/0 | 1590 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0011 | 0/0 | 1590 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0012 | 0/0 | 1590 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0013 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0014 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0015 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0016 | 0/0 | 1590 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0017 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0018 | 0/0 | 1298 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
c0019 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1524 | 193 | 45 | 33 | 92 | 9 | 12 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0002 | 0/0 | 1524 | 63 | 1 | 9 | 42 | 2 | 9 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0003 | 0/0 | 1524 | 59 | 27 | 6 | 13 | 0 | 13 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0004 | 0/0 | 1524 | 46 | 0 | 22 | 15 | 2 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0005 | 0/0 | 1524 | 5 | 5 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0006 | 0/0 | 1524 | 4 | 3 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0007 | 0/0 | 1524 | 3 | 2 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0008 | 0/0 | 1525 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0009 | 0/0 | 1524 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0010 | 0/0 | 1524 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0011 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0012 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0013 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0014 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0015 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
t0016 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0018 | 0/0 | 1298 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0001c0001 | 0/0 | 1590 | 111 | 18 | 16 | 53 | 3 | 21 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0002c0002 | 1/0 | 1590 | 102 | 37 | 22 | 27 | 8 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0002c0016 | 0/0 | 1590 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0003c0003 | 0/1 | 1590 | 79 | 3 | 9 | 62 | 1 | 3 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0003c0015 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0004c0004 | 0/0 | 1590 | 46 | 0 | 22 | 15 | 2 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0004c0007 | 0/0 | 1590 | 7 | 7 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0004c0009 | 0/0 | 1590 | 3 | 2 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0005c0006 | 0/0 | 1590 | 11 | 9 | 2 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0006c0005 | 0/0 | 1590 | 11 | 11 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0007c0008 | 0/0 | 1590 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0008c0010 | 0/0 | 1590 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0009c0012 | 0/0 | 1590 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0010c0011 | 0/0 | 1590 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0011c0013 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0012c0014 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0013c0017 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0014c0019 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0018t0003 | 0/0 | 2821 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0001c0001t0002 | 0/0 | 3113 | 60 | 1 | 9 | 39 | 2 | 9 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0001c0001t0003 | 0/0 | 3113 | 48 | 17 | 6 | 13 | 0 | 12 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0001c0001t0011 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0001c0001t0012 | 0/0 | 3113 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0001c0001t0013 | 0/0 | 3113 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0002c0002t0001 | 1/0 | 3113 | 99 | 34 | 22 | 27 | 8 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0002c0002t0010 | 0/0 | 3113 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0002c0002t0014 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0002c0016t0001 | 0/0 | 3113 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0003c0003t0001 | 0/1 | 3113 | 77 | 2 | 9 | 61 | 1 | 3 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0003c0003t0003 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0003c0003t0015 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0003c0015t0001 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0004c0004t0004 | 0/0 | 3113 | 46 | 0 | 22 | 15 | 2 | 7 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0004c0007t0003 | 0/0 | 3113 | 7 | 7 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0004c0009t0007 | 0/0 | 3113 | 3 | 2 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0005c0006t0001 | 0/0 | 3113 | 7 | 6 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0005c0006t0006 | 0/0 | 3113 | 4 | 3 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0006c0005t0003 | 0/0 | 3113 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0006c0005t0005 | 0/0 | 3113 | 5 | 5 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0006c0005t0008 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0006c0005t0016 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0007c0008t0001 | 0/0 | 3113 | 3 | 3 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0008c0010t0001 | 0/0 | 3113 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0009c0012t0009 | 0/0 | 3113 | 2 | 2 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0010c0011t0002 | 0/0 | 3113 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0011c0013t0001 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0012c0014t0001 | 0/0 | 3113 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0013c0017t0001 | 0/0 | 3113 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
a0014c0019t0002 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | copy fasta | chr14 | 74014349 | 74071092 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0018t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0011g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0001c0001t0013g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0010g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0010g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0002t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0002c0016t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0003t0015g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0003c0015t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0004t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0007t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0007t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0007t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0007t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0007t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0007t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0007t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0009t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0009t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0004c0009t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0005c0006t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0005g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0005g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0005g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0008g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0008g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0008g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0006c0005t0016g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0007c0008t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0007c0008t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0007c0008t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0008c0010t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0008c0010t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0009c0012t0009g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0009c0012t0009g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0010c0011t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0010c0011t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0011c0013t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0012c0014t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0013c0017t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
a0014c0019t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0237 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0160 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0244 | EUR | GBR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0250 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00280 | hp2 | a0004 | c0004 | t0004 | g0101 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00323 | hp1 | a0004 | c0004 | t0004 | g0114 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0056 | EUR | FIN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00423 | hp2 | a0003 | c0003 | t0001 | g0020 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0024 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0057 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00639 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0078 | EAS | CHS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00741 | hp1 | a0004 | c0004 | t0004 | g0089 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01069 | hp2 | a0003 | c0003 | t0001 | g0047 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01070 | hp2 | a0004 | c0004 | t0004 | g0127 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01071 | hp1 | a0004 | c0004 | t0004 | g0002 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0068 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01099 | hp2 | a0004 | c0004 | t0004 | g0096 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01106 | hp2 | a0004 | c0004 | t0004 | g0119 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01109 | hp2 | a0005 | c0006 | t0006 | g0193 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01167 | hp2 | a0004 | c0004 | t0004 | g0092 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0366 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01168 | hp2 | a0004 | c0004 | t0004 | g0095 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01169 | hp1 | a0004 | c0004 | t0004 | g0126 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0076 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01243 | hp1 | a0005 | c0006 | t0001 | g0131 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0191 | AMR | PUR | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01256 | hp1 | a0004 | c0004 | t0004 | g0104 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01256 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01257 | hp1 | a0004 | c0004 | t0004 | g0118 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01258 | hp2 | a0003 | c0003 | t0001 | g0037 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01261 | hp1 | a0004 | c0004 | t0004 | g0108 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01346 | hp1 | a0004 | c0004 | t0004 | g0117 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01433 | hp1 | a0004 | c0004 | t0004 | g0102 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01496 | hp1 | a0001 | c0001 | t0013 | g0302 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0070 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0336 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0251 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0247 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0246 | EUR | IBS | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01884 | hp1 | a0009 | c0012 | t0009 | g0377 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01928 | hp1 | a0004 | c0004 | t0004 | g0124 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01928 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01934 | hp1 | a0004 | c0004 | t0004 | g0105 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01943 | hp2 | a0004 | c0004 | t0004 | g0093 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01981 | hp1 | a0004 | c0004 | t0004 | g0091 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0346 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02015 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02015 | hp2 | a0008 | c0010 | t0001 | g0055 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02040 | hp2 | a0004 | c0004 | t0004 | g0097 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02055 | hp2 | a0006 | c0005 | t0005 | g0373 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02071 | hp1 | a0001 | c0001 | t0011 | g0317 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02071 | hp2 | a0004 | c0004 | t0004 | g0106 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0022 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02129 | hp2 | a0004 | c0004 | t0004 | g0100 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02145 | hp2 | a0004 | c0007 | t0003 | g0361 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02148 | hp2 | a0004 | c0004 | t0004 | g0087 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02165 | hp2 | a0004 | c0004 | t0004 | g0094 | EAS | CDX | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02257 | hp1 | a0006 | c0005 | t0005 | g0371 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02300 | hp1 | a0004 | c0004 | t0004 | g0103 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02300 | hp2 | a0004 | c0004 | t0004 | g0122 | AMR | PEL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02451 | hp2 | a0006 | c0005 | t0008 | g0380 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02572 | hp2 | a0004 | c0009 | t0007 | g0140 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02602 | hp1 | a0000 | c0018 | t0003 | g0175 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02602 | hp2 | a0004 | c0004 | t0004 | g0099 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02622 | hp1 | a0002 | c0002 | t0010 | g0362 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02647 | hp2 | a0004 | c0009 | t0007 | g0138 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02683 | hp1 | a0012 | c0014 | t0001 | g0204 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02698 | hp1 | a0003 | c0003 | t0001 | g0045 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02717 | hp2 | a0002 | c0002 | t0010 | g0363 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0190 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02723 | hp2 | a0006 | c0005 | t0005 | g0369 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02735 | hp2 | a0004 | c0004 | t0004 | g0109 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02738 | hp1 | a0004 | c0004 | t0004 | g0123 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02809 | hp1 | a0004 | c0007 | t0003 | g0007 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02809 | hp2 | a0004 | c0007 | t0003 | g0006 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02818 | hp2 | a0006 | c0005 | t0003 | g0375 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02886 | hp1 | a0006 | c0005 | t0005 | g0372 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02895 | hp2 | a0005 | c0006 | t0001 | g0134 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02897 | hp1 | a0005 | c0006 | t0001 | g0132 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02922 | hp2 | a0007 | c0008 | t0001 | g0216 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02965 | hp1 | a0006 | c0005 | t0003 | g0374 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02970 | hp2 | a0006 | c0005 | t0008 | g0378 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02976 | hp1 | a0007 | c0008 | t0001 | g0273 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0044 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03041 | hp1 | a0004 | c0007 | t0003 | g0004 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03041 | hp2 | a0003 | c0003 | t0003 | g0189 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03130 | hp1 | a0004 | c0007 | t0003 | g0005 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03139 | hp2 | a0009 | c0012 | t0009 | g0376 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03195 | hp2 | a0005 | c0006 | t0006 | g0196 | AFR | ESN | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03209 | hp2 | a0006 | c0005 | t0008 | g0379 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0367 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0200 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03453 | hp2 | a0005 | c0006 | t0006 | g0194 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03486 | hp1 | a0005 | c0006 | t0001 | g0136 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03491 | hp2 | a0004 | c0004 | t0004 | g0115 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03492 | hp1 | a0004 | c0004 | t0004 | g0120 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03540 | hp2 | a0005 | c0006 | t0001 | g0135 | AFR | GWD | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0014 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03927 | hp1 | a0004 | c0004 | t0004 | g0128 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0350 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03942 | hp1 | a0004 | c0004 | t0004 | g0116 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0290 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04184 | hp2 | a0004 | c0009 | t0007 | g0139 | SAS | BEB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04204 | hp1 | a0013 | c0017 | t0001 | g0351 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | STU | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18612 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | CHB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | CHB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18906 | hp1 | a0005 | c0006 | t0001 | g0133 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18906 | hp2 | a0005 | c0006 | t0006 | g0195 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18940 | hp1 | a0014 | c0019 | t0002 | g0291 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18940 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18942 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18942 | hp2 | a0004 | c0004 | t0004 | g0107 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18948 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0382 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18953 | hp1 | a0011 | c0013 | t0001 | g0017 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18956 | hp1 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18957 | hp2 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18960 | hp1 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18961 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18961 | hp2 | a0004 | c0004 | t0004 | g0129 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18962 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18963 | hp1 | a0010 | c0011 | t0002 | g0314 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18963 | hp2 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0065 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18966 | hp1 | a0008 | c0010 | t0001 | g0041 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18966 | hp2 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18967 | hp2 | a0004 | c0004 | t0004 | g0088 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18972 | hp2 | a0004 | c0004 | t0004 | g0111 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18975 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18979 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18983 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18985 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18991 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18997 | hp1 | a0004 | c0004 | t0004 | g0130 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18997 | hp2 | a0003 | c0015 | t0001 | g0059 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0034 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19003 | hp1 | a0004 | c0004 | t0004 | g0113 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19007 | hp2 | a0010 | c0011 | t0002 | g0337 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19009 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19010 | hp2 | a0004 | c0004 | t0004 | g0112 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19012 | hp1 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19043 | hp2 | a0004 | c0007 | t0003 | g0364 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19055 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19057 | hp2 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19062 | hp2 | a0004 | c0004 | t0004 | g0110 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19065 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19070 | hp2 | a0004 | c0004 | t0004 | g0098 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19076 | hp2 | a0003 | c0003 | t0015 | g0027 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19080 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19081 | hp1 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19082 | hp2 | a0004 | c0004 | t0004 | g0125 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19086 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19086 | hp2 | a0004 | c0004 | t0004 | g0121 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19090 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19091 | hp1 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0368 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | YRI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA20129 | hp1 | a0006 | c0005 | t0005 | g0370 | AFR | ASW | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | ASW | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0345 | EUR | TSI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0252 | EUR | TSI | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01123 | hp1 | a0004 | c0004 | t0004 | g0090 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG01123 | hp2 | a0002 | c0016 | t0001 | g0218 | AMR | CLM | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02486 | hp1 | a0005 | c0006 | t0001 | g0137 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02486 | hp2 | a0006 | c0005 | t0016 | g0381 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02559 | hp1 | a0007 | c0008 | t0001 | g0213 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | ACB | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG03471 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | MSL | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
HG06807 | hp2 | a0004 | c0007 | t0003 | g0365 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | USA | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA21309 | hp1 | a0002 | c0002 | t0014 | g0238 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0075 | REF | REF | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0236 | REF | REF | BBOF1_chr14_74014349_74071092 | BBOF1 | chr14 | 74014349 | 74071092 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:74022956
|
A | T | 1 | a0014 | 1 | NA18940.hp1 | stop_gained | HIGH | c.97A>T | p.Lys33* | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 227/3113 | 97/1590 | 33/529 | chr14 | 74022956 | ||
chr14:74022958
|
G | T | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.99G>T | p.Lys33Asn | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 229/3113 | 99/1590 | 33/529 | chr14 | 74022958 | ||
chr14:74022959
|
G | A | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.100G>A | p.Ala34Thr | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 230/3113 | 100/1590 | 34/529 | chr14 | 74022959 | ||
chr14:74022962
|
A | G | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.103A>G | p.Asn35Asp | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 233/3113 | 103/1590 | 35/529 | chr14 | 74022962 | ||
chr14:74022966
|
C | T | 1 | a0014 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.107C>T | p.Ala36Val | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 237/3113 | 107/1590 | 36/529 | chr14 | 74022966 | ||
chr14:74022992
|
G | T | 1 | a0005 | 11 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(8): Show |
missense_variant | MODERATE | c.133G>T | p.Val45Phe | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 263/3113 | 133/1590 | 45/529 | chr14 | 74022992 | ||
chr14:74023032
|
G | A | 4 | a0003a0008a0011others(1): Show | 84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
missense_variant | MODERATE | c.173G>A | p.Arg58Gln | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 303/3113 | 173/1590 | 58/529 | chr14 | 74023032 | ||
chr14:74023079
|
A | C | 2 | a0006a0009 | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
missense_variant | MODERATE | c.220A>C | p.Met74Leu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 350/3113 | 220/1590 | 74/529 | chr14 | 74023079 | ||
chr14:74034152
|
T | A | 1 | a0011 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.476T>A | p.Val159Glu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/12 | 606/3113 | 476/1590 | 159/529 | chr14 | 74034152 | ||
chr14:74040617
|
G | A | 1 | a0006 | 11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
missense_variant | MODERATE | c.548G>A | p.Arg183Lys | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/12 | 678/3113 | 548/1590 | 183/529 | chr14 | 74040617 | ||
chr14:74040629
|
G | T | 1 | a0010 | 2 | NA18963.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.560G>T | p.Arg187Ile | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/12 | 690/3113 | 560/1590 | 187/529 | chr14 | 74040629 | ||
chr14:74047971
|
A | T | 11 | a0000a0001a0003others(8): Show | 277 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(274): Show |
missense_variant | MODERATE | c.689A>T | p.Asp230Val | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/12 | 819/3113 | 689/1590 | 230/529 | chr14 | 74047971 | ||
chr14:74049917
|
G | C | 1 | a0012 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1008G>C | p.Gln336His | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1138/3113 | 1008/1590 | 336/529 | chr14 | 74049917 | ||
chr14:74050077
|
A | G | 1 | a0013 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1168A>G | p.Asn390Asp | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1298/3113 | 1168/1590 | 390/529 | chr14 | 74050077 | ||
chr14:74050177
|
T | C | 1 | a0007 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.1268T>C | p.Leu423Pro | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1398/3113 | 1268/1590 | 423/529 | chr14 | 74050177 | ||
chr14:74050188
|
G | A | 1 | a0008 | 2 | HG02015.hp2 NA18966.hp1 |
missense_variant | MODERATE | c.1279G>A | p.Glu427Lys | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1409/3113 | 1279/1590 | 427/529 | chr14 | 74050188 | ||
chr14:74053659
|
GGCCTCCC others(9771): Show |
G | 1 | a0000 | 1 | HG02602.hp1 | exon_loss_variant | HIGH | c.1287-1913_1579-124 others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 74053659 | |||||
chr14:74057166
|
A | G | 3 | a0001a0010a0014 | 114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
missense_variant | MODERATE | c.1486A>G | p.Lys496Glu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/12 | 1616/3113 | 1486/1590 | 496/529 | chr14 | 74057166 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:74022961
|
C | T | 1 | a0014c0019 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.102C>T | p.Ala34Ala | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/12 | 232/3113 | 102/1590 | 34/529 | chr14 | 74022961 | ||
chr14:74046113
|
C | A | 1 | a0002c0016 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.630C>A | p.Ala210Ala | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/12 | 760/3113 | 630/1590 | 210/529 | chr14 | 74046113 | ||
chr14:74048014
|
C | T | 1 | a0004c0009 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
synonymous_variant | LOW | c.732C>T | p.Asp244Asp | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/12 | 862/3113 | 732/1590 | 244/529 | chr14 | 74048014 | ||
chr14:74049794
|
G | A | 1 | a0004c0004 | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
synonymous_variant | LOW | c.885G>A | p.Leu295Leu | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1015/3113 | 885/1590 | 295/529 | chr14 | 74049794 | ||
chr14:74050157
|
C | T | 1 | a0003c0015 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.1248C>T | p.Thr416Thr | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/12 | 1378/3113 | 1248/1590 | 416/529 | chr14 | 74050157 | ||
chr14:74057246
|
G | A | 6 | a0001c0001a0004c0007a0004c0009others(3): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
synonymous_variant | LOW | c.1566G>A | p.Gln522Gln | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/12 | 1696/3113 | 1566/1590 | 522/529 | chr14 | 74057246 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:74019376
|
G | C | 1 | a0005c0006t0006 | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-103G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/12 | chr14 | 74019376 | ||||||
chr14:74019399
|
C | T | 1 | a0006c0005t0016 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/12 | 80 | chr14 | 74019399 | |||||
chr14:74064781
|
T | C | 1 | a0009c0012t0009 | 2 | HG01884.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*82T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 82 | chr14 | 74064781 | |||||
chr14:74064782
|
T | G | 15 | a0000c0018t0003a0001c0001t0002a0001c0001t0003others(12): Show | 137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*83T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 83 | chr14 | 74064782 | |||||
chr14:74064870
|
G | A | 1 | a0002c0002t0014 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 171 | chr14 | 74064870 | |||||
chr14:74065450
|
A | AT | 1 | a0006c0005t0008 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*754dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 755 | INFO_REALIGN_3_PRIME | chr14 | 74065450 | ||||
chr14:74065582
|
C | A | 1 | a0001c0001t0011 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 883 | chr14 | 74065582 | |||||
chr14:74065584
|
A | C | 1 | a0001c0001t0013 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*885A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 885 | chr14 | 74065584 | |||||
chr14:74065724
|
A | T | 2 | a0006c0005t0005a0006c0005t0016 | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1025A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1025 | chr14 | 74065724 | |||||
chr14:74065820
|
A | C | 4 | a0001c0001t0002a0001c0001t0011a0010c0011t0002others(1): Show | 64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1121A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1121 | chr14 | 74065820 | |||||
chr14:74065828
|
G | A | 1 | a0004c0004t0004 | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1129G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1129 | chr14 | 74065828 | |||||
chr14:74065831
|
T | C | 1 | a0004c0009t0007 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1132T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1132 | chr14 | 74065831 | |||||
chr14:74065986
|
T | A | 1 | a0002c0002t0010 | 2 | HG02622.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1287T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1287 | chr14 | 74065986 | |||||
chr14:74066000
|
A | C | 1 | a0001c0001t0012 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1301 | chr14 | 74066000 | |||||
chr14:74066081
|
T | C | 1 | a0003c0003t0015 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1382T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 12/12 | 1382 | chr14 | 74066081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:74019738
|
A | G | 1 | a0003c0003t0001g0382 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.56+204A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019738 | ||||||
chr14:74019766
|
G | T | 13 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.56+232G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019766 | ||||||
chr14:74019767
|
A | T | 13 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.56+233A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019767 | ||||||
chr14:74019921
|
T | C | 5 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+387T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74019921 | ||||||
chr14:74020064
|
A | G | 1 | a0002c0002t0001g0368 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.56+530A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020064 | ||||||
chr14:74020094
|
A | G | 78 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.56+560A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020094 | ||||||
chr14:74020142
|
A | G | 1 | a0002c0002t0001g0290 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.56+608A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020142 | ||||||
chr14:74020238
|
A | G | 1 | a0002c0002t0001g0289 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56+704A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020238 | ||||||
chr14:74020243
|
AT | A | 286 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(283): Show | 288 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.56+719delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74020243 | |||||
chr14:74020266
|
C | G | 2 | a0001c0001t0002g0366a0001c0001t0002g0367 | 2 | HG01168.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.56+732C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020266 | ||||||
chr14:74020455
|
CAGTG | C | 7 | a0002c0002t0001g0197a0002c0002t0001g0198a0002c0002t0001g0199others(4): Show | 7 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+925_56+928delGA others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74020455 | |||||
chr14:74020505
|
CT | C | 92 | a0002c0002t0001g0197a0002c0002t0001g0198a0002c0002t0001g0199others(89): Show | 92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.56+983delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74020505 | |||||
chr14:74020560
|
A | G | 4 | a0005c0006t0006g0193a0005c0006t0006g0194a0005c0006t0006g0195others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56+1026A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020560 | ||||||
chr14:74020567
|
G | A | 73 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(70): Show | 74 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.56+1033G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020567 | ||||||
chr14:74020584
|
A | G | 1 | a0002c0002t0001g0288 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56+1050A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020584 | ||||||
chr14:74020608
|
A | G | 1 | a0002c0002t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.56+1074A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020608 | ||||||
chr14:74020660
|
C | T | 84 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(81): Show | 84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.56+1126C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020660 | ||||||
chr14:74020818
|
G | A | 73 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(70): Show | 74 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.56+1284G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020818 | ||||||
chr14:74020889
|
A | G | 72 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(69): Show | 73 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.56+1355A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020889 | ||||||
chr14:74020890
|
A | G | 1 | a0014c0019t0002g0291 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.56+1356A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020890 | ||||||
chr14:74020894
|
A | G | 1 | a0014c0019t0002g0291 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.56+1360A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020894 | ||||||
chr14:74020985
|
C | G | 4 | a0005c0006t0006g0193a0005c0006t0006g0194a0005c0006t0006g0195others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.56+1451C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74020985 | ||||||
chr14:74021100
|
A | C | 5 | a0003c0003t0001g0082a0003c0003t0001g0083a0003c0003t0001g0084others(2): Show | 5 | NA18975.hp2 NA18988.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+1566A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021100 | ||||||
chr14:74021317
|
G | T | 3 | a0001c0001t0002g0358a0001c0001t0002g0359a0001c0001t0002g0360 | 3 | NA18983.hp2 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.57-1599G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021317 | ||||||
chr14:74021403
|
T | C | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.57-1513T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021403 | ||||||
chr14:74021465
|
C | A | 11 | a0005c0006t0001g0131a0005c0006t0001g0132a0005c0006t0001g0133others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.57-1451C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021465 | ||||||
chr14:74021581
|
CTT | C | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.57-1334_57-1333del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021581 | ||||||
chr14:74021839
|
G | A | 6 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(3): Show | 6 | HG01081.hp1 HG01884.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-1077G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021839 | ||||||
chr14:74021886
|
G | C | 2 | a0002c0002t0001g0205a0002c0002t0001g0206 | 2 | HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.57-1030G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021886 | ||||||
chr14:74021907
|
T | C | 1 | a0014c0019t0002g0291 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.57-1009T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021907 | ||||||
chr14:74021914
|
G | GA | 6 | a0001c0001t0002g0292a0001c0001t0002g0293a0001c0001t0002g0294others(3): Show | 6 | HG00735.hp1 HG03688.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-990dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74021914 | |||||
chr14:74021944
|
G | A | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.57-972G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74021944 | ||||||
chr14:74022211
|
A | T | 12 | a0002c0002t0001g0001a0002c0002t0001g0277a0002c0002t0001g0278others(9): Show | 14 | HG01358.hp1 HG01952.hp1 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-705A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022211 | ||||||
chr14:74022289
|
T | G | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.57-627T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022289 | ||||||
chr14:74022306
|
C | T | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-610C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022306 | ||||||
chr14:74022310
|
G | T | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-606G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022310 | ||||||
chr14:74022337
|
C | CAGGAGTT others(4): Show |
1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.57-577_57-567dupGG others(9): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74022337 | |||||
chr14:74022416
|
C | T | 1 | a0004c0004t0004g0130 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.57-500C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022416 | ||||||
chr14:74022459
|
G | A | 7 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0008g0378others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-457G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022459 | ||||||
chr14:74022462
|
G | A | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.57-454G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022462 | ||||||
chr14:74022465
|
T | C | 2 | a0002c0002t0001g0205a0002c0002t0001g0206 | 2 | HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.57-451T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022465 | ||||||
chr14:74022467
|
G | A | 3 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57-449G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022467 | ||||||
chr14:74022522
|
C | T | 77 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(74): Show | 78 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.57-394C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022522 | ||||||
chr14:74022523
|
G | A | 1 | a0003c0003t0001g0009 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.57-393G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022523 | ||||||
chr14:74022541
|
A | T | 78 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.57-375A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022541 | ||||||
chr14:74022552
|
GA | G | 7 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(4): Show | 7 | HG01081.hp1 HG01884.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-354delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 74022552 | |||||
chr14:74022645
|
A | G | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.57-271A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022645 | ||||||
chr14:74022710
|
T | C | 1 | a0003c0003t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.57-206T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022710 | ||||||
chr14:74022711
|
C | T | 1 | a0003c0003t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.57-205C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 1/11 | chr14 | 74022711 | ||||||
chr14:74023299
|
T | G | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+155T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023299 | ||||||
chr14:74023342
|
C | T | 40 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.285+198C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023342 | ||||||
chr14:74023448
|
T | C | 1 | a0002c0002t0001g0208 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.285+304T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023448 | ||||||
chr14:74023553
|
C | T | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+409C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023553 | ||||||
chr14:74023573
|
A | T | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.285+429A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023573 | ||||||
chr14:74023658
|
G | A | 1 | a0002c0002t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.285+514G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023658 | ||||||
chr14:74023745
|
G | A | 5 | a0001c0001t0003g0149a0001c0001t0003g0150a0002c0002t0001g0147others(2): Show | 5 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+601G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023745 | ||||||
chr14:74023841
|
G | A | 2 | a0003c0003t0001g0011a0003c0003t0001g0012 | 2 | HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.285+697G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023841 | ||||||
chr14:74023857
|
A | G | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+713A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023857 | ||||||
chr14:74023920
|
C | T | 1 | a0003c0003t0001g0081 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.285+776C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023920 | ||||||
chr14:74023925
|
C | CA | 11 | a0001c0001t0002g0297a0001c0001t0003g0298a0001c0001t0003g0299others(8): Show | 11 | HG00438.hp1 HG01109.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+799dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74023925 | |||||
chr14:74023925
|
CA | C | 8 | a0001c0001t0002g0356a0001c0001t0002g0357a0001c0001t0003g0188others(5): Show | 8 | HG02451.hp2 HG02976.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+799delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74023925 | |||||
chr14:74023961
|
G | A | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+817G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74023961 | ||||||
chr14:74024230
|
T | A | 1 | a0002c0002t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.285+1086T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024230 | ||||||
chr14:74024349
|
G | A | 5 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+1205G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024349 | ||||||
chr14:74024362
|
G | A | 84 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(81): Show | 84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.285+1218G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024362 | ||||||
chr14:74024414
|
T | G | 6 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+1270T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024414 | ||||||
chr14:74024418
|
G | C | 64 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.285+1274G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024418 | ||||||
chr14:74024419
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.285+1275G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024419 | ||||||
chr14:74024542
|
C | T | 2 | a0002c0002t0001g0271a0002c0002t0001g0272 | 2 | HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.285+1398C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024542 | ||||||
chr14:74024550
|
C | T | 2 | a0001c0001t0002g0354a0001c0001t0002g0355 | 2 | NA18954.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.285+1406C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024550 | ||||||
chr14:74024557
|
C | T | 5 | a0001c0001t0003g0149a0001c0001t0003g0150a0002c0002t0001g0147others(2): Show | 5 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+1413C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024557 | ||||||
chr14:74024582
|
A | G | 14 | a0005c0006t0001g0131a0005c0006t0001g0132a0005c0006t0001g0133others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.285+1438A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024582 | ||||||
chr14:74024627
|
G | A | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+1483G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024627 | ||||||
chr14:74024713
|
G | A | 1 | a0003c0003t0001g0014 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.285+1569G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024713 | ||||||
chr14:74024748
|
G | T | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.285+1604G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024748 | ||||||
chr14:74024932
|
T | G | 12 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(9): Show | 12 | HG00408.hp1 HG02083.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.285+1788T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024932 | ||||||
chr14:74024948
|
A | G | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.285+1804A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74024948 | ||||||
chr14:74025023
|
C | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.285+1879C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025023 | ||||||
chr14:74025127
|
A | G | 2 | a0003c0003t0001g0190a0003c0003t0001g0191 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.285+1983A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025127 | ||||||
chr14:74025159
|
C | T | 11 | a0005c0006t0001g0131a0005c0006t0001g0132a0005c0006t0001g0133others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+2015C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025159 | ||||||
chr14:74025163
|
A | G | 5 | a0001c0001t0003g0149a0001c0001t0003g0150a0002c0002t0001g0147others(2): Show | 5 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+2019A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025163 | ||||||
chr14:74025565
|
A | C | 1 | a0002c0002t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.285+2421A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025565 | ||||||
chr14:74025905
|
T | TG | 82 | a0001c0001t0003g0152a0002c0002t0001g0212a0003c0003t0001g0008others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.285+2769dupG | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74025905 | |||||
chr14:74025906
|
G | A | 7 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0008g0378others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+2762G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025906 | ||||||
chr14:74025907
|
G | C | 1 | a0001c0001t0003g0151 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.285+2763G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74025907 | ||||||
chr14:74026140
|
C | CA | 66 | a0001c0001t0002g0315a0002c0002t0001g0197a0002c0002t0001g0198others(63): Show | 67 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.285+3010dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026140 | |||||
chr14:74026140
|
C | CAA | 7 | a0005c0006t0001g0131a0005c0006t0001g0132a0005c0006t0001g0133others(4): Show | 7 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3009_285+3010d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026140 | |||||
chr14:74026140
|
CA | C | 7 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0003g0188others(4): Show | 7 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3010delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026140 | |||||
chr14:74026153
|
A | G | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+3009A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026153 | ||||||
chr14:74026263
|
G | A | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-2921G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026263 | ||||||
chr14:74026271
|
A | G | 64 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.286-2913A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026271 | ||||||
chr14:74026310
|
T | G | 63 | a0002c0002t0001g0197a0002c0002t0001g0198a0002c0002t0001g0199others(60): Show | 64 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.286-2874T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026310 | ||||||
chr14:74026444
|
C | CA | 165 | a0001c0001t0002g0003a0001c0001t0002g0293a0001c0001t0002g0294others(162): Show | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.286-2716dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026444 | |||||
chr14:74026444
|
C | CAA | 19 | a0001c0001t0002g0292a0001c0001t0002g0297a0001c0001t0002g0316others(16): Show | 19 | HG00741.hp1 HG01167.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.286-2717_286-2716d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026444 | |||||
chr14:74026444
|
CA | C | 12 | a0001c0001t0003g0182a0001c0001t0003g0183a0001c0001t0003g0184others(9): Show | 12 | HG01934.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-2716delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026444 | |||||
chr14:74026505
|
A | T | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2679A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026505 | ||||||
chr14:74026509
|
T | A | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2675T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026509 | ||||||
chr14:74026511
|
A | T | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2673A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026511 | ||||||
chr14:74026538
|
T | C | 224 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(221): Show | 226 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.286-2646T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026538 | ||||||
chr14:74026702
|
A | G | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-2482A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026702 | ||||||
chr14:74026791
|
A | T | 1 | a0003c0003t0001g0008 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-2393A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026791 | ||||||
chr14:74026820
|
G | A | 1 | a0001c0001t0002g0319 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.286-2364G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026820 | ||||||
chr14:74026930
|
GAA | G | 78 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-2243_286-2242d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74026930 | |||||
chr14:74026931
|
A | G | 1 | a0004c0004t0004g0130 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.286-2253A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026931 | ||||||
chr14:74026989
|
A | T | 28 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(25): Show | 28 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.286-2195A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74026989 | ||||||
chr14:74027082
|
C | CT | 177 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(174): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.286-2080dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | |||||
chr14:74027082
|
C | CTT | 37 | a0001c0001t0003g0155a0001c0001t0003g0176a0001c0001t0003g0177others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.286-2081_286-2080d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | |||||
chr14:74027082
|
CT | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0293a0001c0001t0002g0294others(57): Show | 61 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.286-2080delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | |||||
chr14:74027082
|
CTTT | C | 15 | a0003c0003t0001g0009a0003c0003t0001g0023a0003c0003t0001g0024others(12): Show | 15 | HG00544.hp2 NA18940.hp2 NA18942.hp1 others(12): Show |
intron_variant | MODIFIER | c.286-2082_286-2080d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027082 | |||||
chr14:74027203
|
A | G | 1 | a0001c0001t0002g0319 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.286-1981A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027203 | ||||||
chr14:74027271
|
A | G | 381 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(378): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.286-1913A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027271 | ||||||
chr14:74027304
|
C | A | 1 | a0004c0004t0004g0090 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.286-1880C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027304 | ||||||
chr14:74027378
|
C | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.286-1806C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027378 | ||||||
chr14:74027385
|
C | CT | 125 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0293others(122): Show | 126 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.286-1773dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | |||||
chr14:74027385
|
C | CTT | 51 | a0001c0001t0002g0294a0001c0001t0002g0297a0001c0001t0002g0305others(48): Show | 51 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.286-1774_286-1773d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | |||||
chr14:74027385
|
C | CTTT | 8 | a0001c0001t0002g0292a0001c0001t0002g0309a0001c0001t0002g0311others(5): Show | 8 | HG00408.hp1 HG02895.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-1775_286-1773d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | |||||
chr14:74027385
|
CT | C | 43 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0147others(40): Show | 44 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.286-1773delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | |||||
chr14:74027385
|
CTT | C | 13 | a0002c0002t0001g0197a0002c0002t0001g0198a0002c0002t0001g0199others(10): Show | 13 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-1774_286-1773d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | |||||
chr14:74027385
|
CTTT | C | 6 | a0004c0007t0003g0004a0005c0006t0001g0132a0005c0006t0001g0133others(3): Show | 6 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-1775_286-1773d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027385 | |||||
chr14:74027449
|
T | C | 2 | a0009c0012t0009g0376a0009c0012t0009g0377 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.286-1735T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027449 | ||||||
chr14:74027604
|
G | T | 1 | a0002c0002t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.286-1580G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027604 | ||||||
chr14:74027734
|
A | G | 78 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-1450A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027734 | ||||||
chr14:74027736
|
C | G | 1 | a0003c0003t0001g0031 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.286-1448C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027736 | ||||||
chr14:74027911
|
T | TACAAGAA others(6): Show |
1 | a0001c0001t0002g0315 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.286-1272_286-1271i others(15): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74027911 | |||||
chr14:74027915
|
C | A | 1 | a0001c0001t0002g0315 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.286-1269C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027915 | ||||||
chr14:74027918
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.286-1266G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027918 | ||||||
chr14:74027933
|
G | T | 1 | a0005c0006t0006g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286-1251G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74027933 | ||||||
chr14:74028347
|
C | T | 3 | a0004c0009t0007g0138a0004c0009t0007g0139a0004c0009t0007g0140 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.286-837C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028347 | ||||||
chr14:74028387
|
C | G | 78 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(75): Show | 79 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-797C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028387 | ||||||
chr14:74028467
|
T | TAC | 39 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0157others(36): Show | 39 | HG00544.hp1 HG00673.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.286-673_286-672dup others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
T | TACAC | 17 | a0000c0018t0003g0175a0001c0001t0003g0149a0001c0001t0003g0150others(14): Show | 17 | HG00408.hp2 HG01074.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.286-675_286-672dup others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
T | TACACAC | 4 | a0001c0001t0003g0152a0001c0001t0003g0158a0001c0001t0003g0181others(1): Show | 4 | HG02486.hp2 HG03831.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-677_286-672dup others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
T | TACACACA others(3): Show |
1 | a0001c0001t0003g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.286-681_286-672dup others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
T | TACACACA others(5): Show |
1 | a0001c0001t0003g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.286-683_286-672dup others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TAC | T | 28 | a0001c0001t0003g0159a0001c0001t0003g0161a0001c0001t0003g0162others(25): Show | 28 | HG00099.hp2 HG00438.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.286-673_286-672del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TACAC | T | 79 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(76): Show | 82 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.286-675_286-672del others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TACACAC | T | 11 | a0002c0002t0001g0230a0002c0002t0001g0264a0002c0002t0001g0289others(8): Show | 11 | HG00558.hp1 HG00642.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-677_286-672del others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TACACACA others(1): Show |
T | 4 | a0002c0002t0001g0197a0002c0002t0001g0285a0002c0016t0001g0218others(1): Show | 4 | HG01123.hp2 HG02818.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-679_286-672del others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TACACACA others(5): Show |
T | 5 | a0004c0007t0003g0007a0005c0006t0006g0193a0005c0006t0006g0194others(2): Show | 5 | HG01109.hp2 HG02809.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-683_286-672del others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TACACACA others(7): Show |
T | 1 | a0002c0002t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-685_286-672del others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TACACACA others(9): Show |
T | 14 | a0002c0002t0001g0208a0002c0002t0001g0210a0002c0002t0001g0211others(11): Show | 14 | HG01070.hp1 HG01192.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.286-687_286-672del others(16): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028467
|
TACACACA others(13): Show |
T | 12 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(9): Show | 12 | HG00408.hp1 HG02083.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-691_286-672del others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028467 | |||||
chr14:74028503
|
C | G | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-681C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028503 | ||||||
chr14:74028507
|
C | A | 16 | a0001c0001t0002g0294a0001c0001t0002g0297a0001c0001t0002g0318others(13): Show | 16 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.286-677C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028507 | ||||||
chr14:74028509
|
C | A | 86 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(83): Show | 87 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.286-675C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028509 | ||||||
chr14:74028509
|
C | CAA | 55 | a0003c0003t0001g0009a0003c0003t0001g0011a0003c0003t0001g0013others(52): Show | 55 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.286-674_286-673ins others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028509 | |||||
chr14:74028509
|
C | T | 16 | a0001c0001t0002g0294a0001c0001t0002g0297a0001c0001t0002g0318others(13): Show | 16 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.286-675C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028509 | ||||||
chr14:74028511
|
C | G | 18 | a0001c0001t0002g0294a0001c0001t0002g0297a0001c0001t0002g0318others(15): Show | 18 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.286-673C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028511 | ||||||
chr14:74028511
|
C | T | 141 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(138): Show | 142 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.286-673C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028511 | ||||||
chr14:74028513
|
A | C | 1 | a0001c0001t0003g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.286-671A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028513 | ||||||
chr14:74028513
|
A | G | 141 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(138): Show | 142 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.286-671A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028513 | ||||||
chr14:74028513
|
AAT | A | 18 | a0001c0001t0002g0294a0001c0001t0002g0297a0001c0001t0002g0318others(15): Show | 18 | HG01109.hp1 HG01981.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.286-669_286-668del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028513 | |||||
chr14:74028515
|
T | A | 142 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(139): Show | 143 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.286-669T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028515 | ||||||
chr14:74028515
|
T | TAGAA | 64 | a0001c0001t0003g0296a0001c0001t0003g0298a0001c0001t0003g0299others(61): Show | 65 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.286-666_286-665ins others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028515 | |||||
chr14:74028638
|
G | A | 2 | a0003c0003t0001g0030a0003c0003t0001g0034 | 2 | NA18979.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.286-546G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028638 | ||||||
chr14:74028731
|
CAG | C | 3 | a0003c0003t0001g0053a0003c0003t0001g0054a0003c0003t0001g0069 | 3 | NA18966.hp2 NA18985.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.286-450_286-449del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028731 | |||||
chr14:74028744
|
T | C | 2 | a0009c0012t0009g0376a0009c0012t0009g0377 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.286-440T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028744 | ||||||
chr14:74028751
|
C | T | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.286-433C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028751 | ||||||
chr14:74028763
|
C | T | 2 | a0001c0001t0003g0153a0001c0001t0003g0154 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.286-421C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028763 | ||||||
chr14:74028766
|
T | C | 1 | a0002c0002t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.286-418T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028766 | ||||||
chr14:74028777
|
C | T | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-407C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028777 | ||||||
chr14:74028831
|
C | T | 2 | a0002c0002t0001g0231a0002c0002t0001g0237 | 2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.286-353C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | chr14 | 74028831 | ||||||
chr14:74028948
|
C | CCACA | 40 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-219_286-216dup others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028948 | |||||
chr14:74028948
|
CCA | C | 226 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(223): Show | 228 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.286-217_286-216del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 74028948 | |||||
chr14:74029375
|
T | C | 1 | a0001c0001t0003g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.351+126T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029375 | ||||||
chr14:74029458
|
G | A | 7 | a0002c0002t0001g0197a0002c0002t0001g0198a0002c0002t0001g0199others(4): Show | 7 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+209G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029458 | ||||||
chr14:74029617
|
A | G | 266 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(263): Show | 268 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.351+368A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029617 | ||||||
chr14:74029636
|
C | T | 1 | a0001c0001t0002g0343 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.351+387C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029636 | ||||||
chr14:74029682
|
C | CA | 47 | a0000c0018t0003g0175a0001c0001t0002g0343a0001c0001t0003g0151others(44): Show | 47 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.351+448dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74029682 | |||||
chr14:74029682
|
CA | C | 6 | a0003c0003t0001g0019a0003c0003t0001g0052a0003c0003t0001g0074others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+448delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74029682 | |||||
chr14:74029780
|
A | G | 4 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0229others(1): Show | 4 | NA18952.hp2 NA19010.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+531A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74029780 | ||||||
chr14:74030079
|
A | G | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.351+830A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030079 | ||||||
chr14:74030082
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.351+833C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030082 | ||||||
chr14:74030527
|
G | A | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+1278G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030527 | ||||||
chr14:74030686
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.351+1437G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030686 | ||||||
chr14:74030760
|
G | A | 64 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.351+1511G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030760 | ||||||
chr14:74030855
|
T | G | 1 | a0009c0012t0009g0377 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.351+1606T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030855 | ||||||
chr14:74030859
|
T | A | 1 | a0001c0001t0002g0354 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.351+1610T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030859 | ||||||
chr14:74030860
|
A | T | 1 | a0001c0001t0002g0354 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.351+1611A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030860 | ||||||
chr14:74030921
|
C | CAT | 3 | a0002c0002t0001g0252a0002c0002t0001g0255a0002c0002t0001g0276 | 3 | HG02970.hp1 HG03239.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.351+1690_351+1691d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030921 | |||||
chr14:74030921
|
CAT | C | 205 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(202): Show | 207 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.351+1690_351+1691d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030921 | |||||
chr14:74030931
|
T | G | 2 | a0002c0002t0010g0362a0002c0002t0010g0363 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.351+1682T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030931 | ||||||
chr14:74030933
|
T | G | 9 | a0001c0001t0002g0320a0001c0001t0003g0158a0001c0001t0003g0174others(6): Show | 9 | HG00408.hp2 HG01069.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+1684T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030933 | ||||||
chr14:74030933
|
T | TAG | 7 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0182others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+1685_351+1686i others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030933 | |||||
chr14:74030933
|
T | TAGAG | 18 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(15): Show | 18 | HG00099.hp2 HG00544.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.351+1685_351+1686i others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030933 | |||||
chr14:74030935
|
T | G | 69 | a0000c0018t0003g0175a0001c0001t0002g0320a0001c0001t0002g0321others(66): Show | 69 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.351+1686T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030935 | ||||||
chr14:74030935
|
T | TAG | 4 | a0001c0001t0003g0157a0001c0001t0003g0183a0001c0001t0003g0274others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1687_351+1688i others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030935 | |||||
chr14:74030935
|
T | TAGAG | 7 | a0001c0001t0003g0159a0001c0001t0003g0166a0001c0001t0003g0167others(4): Show | 7 | HG00438.hp2 HG03669.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+1687_351+1688i others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030935 | |||||
chr14:74030937
|
T | G | 176 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0293others(173): Show | 177 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.351+1688T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030937 | ||||||
chr14:74030937
|
T | TAG | 6 | a0001c0001t0003g0156a0002c0002t0001g0242a0002c0016t0001g0218others(3): Show | 6 | HG01074.hp2 HG01123.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1689_351+1690i others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030937 | |||||
chr14:74030939
|
T | G | 297 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0293others(294): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.351+1690T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030939 | ||||||
chr14:74030939
|
TAG | T | 5 | a0003c0003t0001g0051a0003c0003t0001g0086a0003c0015t0001g0059others(2): Show | 5 | HG02738.hp1 HG02818.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+1702_351+1703d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74030939 | |||||
chr14:74030941
|
G | T | 1 | a0002c0002t0001g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.351+1692G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74030941 | ||||||
chr14:74031012
|
G | A | 2 | a0001c0001t0003g0162a0001c0001t0003g0168 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.351+1763G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031012 | ||||||
chr14:74031119
|
C | CTT | 6 | a0001c0001t0002g0354a0002c0002t0010g0362a0002c0002t0010g0363others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1881_351+1882d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74031119 | |||||
chr14:74031119
|
C | CTTT | 72 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(69): Show | 73 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.351+1880_351+1882d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74031119 | |||||
chr14:74031140
|
G | C | 7 | a0001c0001t0003g0298a0001c0001t0003g0299a0001c0001t0003g0300others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+1891G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031140 | ||||||
chr14:74031350
|
C | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(70): Show | 74 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.351+2101C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031350 | ||||||
chr14:74031370
|
C | T | 2 | a0004c0004t0004g0115a0004c0004t0004g0120 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.351+2121C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031370 | ||||||
chr14:74031499
|
T | A | 3 | a0003c0003t0001g0042a0003c0003t0001g0043a0003c0003t0001g0082 | 3 | NA19057.hp2 NA19081.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.351+2250T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031499 | ||||||
chr14:74031512
|
T | A | 1 | a0001c0001t0012g0160 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.351+2263T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031512 | ||||||
chr14:74031589
|
G | C | 2 | a0002c0002t0001g0219a0002c0002t0001g0232 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.351+2340G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031589 | ||||||
chr14:74031630
|
G | A | 229 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(226): Show | 231 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.351+2381G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031630 | ||||||
chr14:74031655
|
A | G | 229 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(226): Show | 231 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.352-2373A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031655 | ||||||
chr14:74031845
|
T | A | 1 | a0001c0001t0003g0151 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.352-2183T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031845 | ||||||
chr14:74031945
|
G | A | 5 | a0002c0002t0010g0362a0002c0002t0010g0363a0004c0007t0003g0361others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-2083G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74031945 | ||||||
chr14:74032092
|
A | G | 1 | a0004c0004t0004g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.352-1936A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032092 | ||||||
chr14:74032118
|
A | AT | 96 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0152others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.352-1885dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | |||||
chr14:74032118
|
A | ATT | 14 | a0002c0002t0001g0192a0003c0003t0001g0011a0003c0003t0001g0014others(11): Show | 14 | HG01243.hp2 HG01928.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.352-1886_352-1885d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | |||||
chr14:74032118
|
AT | A | 8 | a0001c0001t0002g0354a0002c0002t0001g0208a0002c0002t0001g0223others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-1885delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | |||||
chr14:74032118
|
ATT | A | 10 | a0001c0001t0002g0305a0001c0001t0002g0340a0001c0001t0002g0349others(7): Show | 10 | HG02135.hp2 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.352-1886_352-1885d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | |||||
chr14:74032118
|
ATTT | A | 65 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(62): Show | 66 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.352-1887_352-1885d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032118 | |||||
chr14:74032126
|
T | A | 36 | a0004c0004t0004g0089a0004c0004t0004g0090a0004c0004t0004g0091others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.352-1902T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032126 | ||||||
chr14:74032133
|
T | A | 9 | a0004c0004t0004g0089a0004c0004t0004g0099a0004c0004t0004g0100others(6): Show | 9 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.352-1895T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032133 | ||||||
chr14:74032148
|
C | A | 2 | a0003c0003t0001g0037a0003c0003t0001g0060 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.352-1880C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032148 | ||||||
chr14:74032212
|
C | T | 3 | a0004c0004t0004g0090a0004c0004t0004g0103a0004c0004t0004g0108 | 3 | HG01123.hp1 HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.352-1816C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032212 | ||||||
chr14:74032257
|
G | A | 1 | a0004c0007t0003g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.352-1771G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032257 | ||||||
chr14:74032450
|
A | T | 8 | a0003c0003t0001g0039a0003c0003t0001g0050a0003c0003t0001g0053others(5): Show | 8 | HG00673.hp2 HG02015.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1578A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032450 | ||||||
chr14:74032489
|
C | CT | 127 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(124): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.352-1525dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74032489 | |||||
chr14:74032491
|
T | C | 1 | a0002c0002t0001g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.352-1537T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032491 | ||||||
chr14:74032553
|
G | A | 1 | a0001c0001t0002g0328 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.352-1475G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032553 | ||||||
chr14:74032727
|
C | T | 41 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(38): Show | 41 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.352-1301C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032727 | ||||||
chr14:74032854
|
G | A | 11 | a0001c0001t0003g0298a0001c0001t0003g0299a0001c0001t0003g0301others(8): Show | 11 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.352-1174G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74032854 | ||||||
chr14:74033216
|
AT | A | 59 | a0003c0003t0003g0189a0004c0004t0004g0002a0004c0004t0004g0087others(56): Show | 60 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.352-805delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 74033216 | |||||
chr14:74033227
|
A | G | 7 | a0003c0003t0001g0018a0003c0003t0001g0026a0003c0003t0001g0032others(4): Show | 7 | NA18940.hp2 NA18959.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-801A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033227 | ||||||
chr14:74033256
|
A | T | 4 | a0002c0002t0001g0242a0002c0002t0001g0255a0002c0002t0001g0269others(1): Show | 4 | HG01123.hp2 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-772A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033256 | ||||||
chr14:74033268
|
A | G | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.352-760A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033268 | ||||||
chr14:74033280
|
A | G | 3 | a0004c0009t0007g0138a0004c0009t0007g0139a0004c0009t0007g0140 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.352-748A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033280 | ||||||
chr14:74033421
|
T | C | 1 | a0004c0004t0004g0090 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.352-607T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033421 | ||||||
chr14:74033491
|
A | C | 2 | a0009c0012t0009g0376a0009c0012t0009g0377 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.352-537A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033491 | ||||||
chr14:74033564
|
C | T | 1 | a0004c0004t0004g0126 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.352-464C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033564 | ||||||
chr14:74033779
|
T | G | 1 | a0004c0004t0004g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.352-249T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033779 | ||||||
chr14:74033808
|
G | A | 1 | a0003c0003t0001g0011 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.352-220G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033808 | ||||||
chr14:74033827
|
T | C | 114 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-201T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033827 | ||||||
chr14:74033845
|
G | A | 3 | a0004c0004t0004g0094a0004c0004t0004g0106a0004c0004t0004g0107 | 3 | HG02071.hp2 HG02165.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.352-183G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033845 | ||||||
chr14:74033882
|
A | T | 114 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-146A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033882 | ||||||
chr14:74033883
|
T | A | 114 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.352-145T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033883 | ||||||
chr14:74033888
|
A | C | 6 | a0005c0006t0001g0131a0005c0006t0001g0132a0005c0006t0001g0133others(3): Show | 6 | HG01243.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-140A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033888 | ||||||
chr14:74033918
|
G | A | 40 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.352-110G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 3/11 | chr14 | 74033918 | ||||||
chr14:74034239
|
A | G | 1 | a0004c0004t0004g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.495+68A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034239 | ||||||
chr14:74034331
|
A | C | 132 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(129): Show | 133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.495+160A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034331 | ||||||
chr14:74034481
|
A | G | 3 | a0004c0009t0007g0138a0004c0009t0007g0139a0004c0009t0007g0140 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.495+310A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034481 | ||||||
chr14:74034566
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.495+395G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034566 | ||||||
chr14:74034747
|
C | G | 149 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(146): Show | 150 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.495+576C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034747 | ||||||
chr14:74034833
|
G | A | 6 | a0002c0002t0001g0239a0002c0002t0001g0240a0002c0002t0001g0246others(3): Show | 6 | HG00639.hp2 HG01261.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+662G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034833 | ||||||
chr14:74034963
|
G | A | 83 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.495+792G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74034963 | ||||||
chr14:74035009
|
T | C | 81 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(78): Show | 81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.495+838T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035009 | ||||||
chr14:74035077
|
A | G | 276 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(273): Show | 278 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.495+906A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035077 | ||||||
chr14:74035138
|
T | C | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.495+967T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035138 | ||||||
chr14:74035226
|
TA | T | 51 | a0002c0002t0001g0001a0002c0002t0001g0205a0002c0002t0001g0206others(48): Show | 53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.495+1065delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035226 | |||||
chr14:74035290
|
A | C | 275 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(272): Show | 277 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.495+1119A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035290 | ||||||
chr14:74035298
|
A | G | 40 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.495+1127A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035298 | ||||||
chr14:74035377
|
C | T | 3 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.495+1206C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035377 | ||||||
chr14:74035413
|
C | CT | 18 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(15): Show | 18 | HG00735.hp1 HG01081.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1263dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | |||||
chr14:74035413
|
CT | C | 141 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(138): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.495+1263delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | |||||
chr14:74035413
|
CTT | C | 19 | a0001c0001t0002g0333a0001c0001t0003g0149a0001c0001t0003g0150others(16): Show | 19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.495+1262_495+1263d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | |||||
chr14:74035413
|
CTTT | C | 8 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(5): Show | 8 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+1261_495+1263d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035413 | |||||
chr14:74035453
|
A | G | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.495+1282A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035453 | ||||||
chr14:74035480
|
G | A | 4 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1309G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035480 | ||||||
chr14:74035527
|
G | A | 2 | a0003c0003t0001g0190a0003c0003t0001g0191 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.495+1356G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035527 | ||||||
chr14:74035542
|
C | T | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.495+1371C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035542 | ||||||
chr14:74035567
|
A | G | 3 | a0007c0008t0001g0213a0007c0008t0001g0216a0007c0008t0001g0273 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.495+1396A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035567 | ||||||
chr14:74035578
|
C | G | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+1407C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035578 | ||||||
chr14:74035584
|
A | AT | 22 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(19): Show | 22 | HG00735.hp1 HG01109.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.495+1441dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTT | 39 | a0001c0001t0002g0313a0001c0001t0002g0331a0001c0001t0003g0149others(36): Show | 39 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.495+1439_495+1441d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTT | 56 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(53): Show | 57 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.495+1438_495+1441d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTT | 15 | a0001c0001t0002g0297a0001c0001t0002g0306a0001c0001t0002g0316others(12): Show | 15 | HG00423.hp1 HG00735.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.495+1437_495+1441d others(7): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(3): Show |
4 | a0004c0007t0003g0361a0006c0005t0005g0369a0006c0005t0005g0370others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1432_495+1441d others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(4): Show |
2 | a0006c0005t0005g0373a0006c0005t0016g0381 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.495+1431_495+1441d others(13): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(5): Show |
1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.495+1430_495+1441d others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(6): Show |
1 | a0006c0005t0005g0372 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.495+1429_495+1441d others(15): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(8): Show |
1 | a0006c0005t0003g0375 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.495+1427_495+1441d others(17): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(11): Show |
2 | a0004c0007t0003g0004a0004c0007t0003g0006 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.495+1424_495+1441d others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(12): Show |
1 | a0004c0007t0003g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.495+1423_495+1441d others(21): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(21): Show |
1 | a0006c0005t0008g0380 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.495+1414_495+1441d others(30): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
A | ATTTTTTT others(22): Show |
2 | a0006c0005t0008g0378a0006c0005t0008g0379 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.495+1441_495+1442i others(31): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
AT | A | 114 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(111): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.495+1441delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035584
|
ATTTTTTT others(4): Show |
A | 1 | a0004c0007t0003g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.495+1431_495+1441d others(13): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74035584 | |||||
chr14:74035712
|
C | T | 1 | a0002c0002t0001g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+1541C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035712 | ||||||
chr14:74035792
|
C | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+1621C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035792 | ||||||
chr14:74035810
|
C | T | 11 | a0001c0001t0002g0339a0004c0007t0003g0004a0004c0007t0003g0005others(8): Show | 11 | HG00673.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+1639C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035810 | ||||||
chr14:74035854
|
A | T | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.495+1683A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035854 | ||||||
chr14:74035856
|
TCACA | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+1686_495+1689d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035856 | ||||||
chr14:74035903
|
G | A | 1 | a0006c0005t0016g0381 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.495+1732G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74035903 | ||||||
chr14:74036062
|
C | CT | 12 | a0002c0002t0001g0001a0002c0002t0001g0277a0002c0002t0001g0278others(9): Show | 14 | HG01358.hp1 HG01884.hp1 HG03139.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+1902dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036062 | |||||
chr14:74036062
|
CT | C | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1902delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036062 | |||||
chr14:74036118
|
C | T | 114 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.495+1947C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036118 | ||||||
chr14:74036135
|
AACCTCC | A | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1971_495+1976d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036135 | |||||
chr14:74036174
|
G | C | 84 | a0002c0002t0001g0261a0003c0003t0001g0008a0003c0003t0001g0009others(81): Show | 84 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.495+2003G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036174 | ||||||
chr14:74036184
|
T | G | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.495+2013T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036184 | ||||||
chr14:74036210
|
C | T | 3 | a0007c0008t0001g0213a0007c0008t0001g0216a0007c0008t0001g0273 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.495+2039C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036210 | ||||||
chr14:74036498
|
C | T | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.495+2327C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036498 | ||||||
chr14:74036630
|
A | G | 376 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(373): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.495+2459A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036630 | ||||||
chr14:74036683
|
C | CA | 275 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.495+2530dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036683 | |||||
chr14:74036683
|
C | CAA | 46 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0342others(43): Show | 46 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+2529_495+2530d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036683 | |||||
chr14:74036683
|
CA | C | 44 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(41): Show | 45 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.495+2530delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036683 | |||||
chr14:74036701
|
A | G | 1 | a0004c0007t0003g0361 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.495+2530A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036701 | ||||||
chr14:74036702
|
G | A | 1 | a0006c0005t0003g0375 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.495+2531G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036702 | ||||||
chr14:74036782
|
G | A | 48 | a0002c0002t0001g0001a0002c0002t0001g0205a0002c0002t0001g0206others(45): Show | 50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.495+2611G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036782 | ||||||
chr14:74036905
|
T | G | 4 | a0005c0006t0006g0193a0005c0006t0006g0194a0005c0006t0006g0195others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+2734T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74036905 | ||||||
chr14:74036952
|
ATCTTTTT others(12): Show |
A | 8 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+2795_495+2813d others(21): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036952 | |||||
chr14:74036954
|
CTTTTTTT others(13): Show |
C | 2 | a0004c0009t0007g0138a0004c0009t0007g0140 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.495+2795_495+2814d others(22): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036954 | |||||
chr14:74036955
|
TTTTTTTT others(11): Show |
T | 3 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0016g0381 | 3 | HG02486.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.495+2795_495+2812d others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036955 | |||||
chr14:74036973
|
C | CT | 20 | a0002c0002t0001g0222a0002c0002t0001g0233a0002c0002t0001g0289others(17): Show | 20 | HG00738.hp1 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.495+2819dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74036973 | |||||
chr14:74037009
|
G | A | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.495+2838G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037009 | ||||||
chr14:74037119
|
C | T | 4 | a0002c0002t0001g0147a0002c0002t0001g0148a0002c0002t0001g0192others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+2948C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037119 | ||||||
chr14:74037156
|
G | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.495+2985G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037156 | ||||||
chr14:74037226
|
G | A | 16 | a0001c0001t0003g0155a0001c0001t0003g0158a0001c0001t0003g0159others(13): Show | 16 | HG00099.hp2 HG00438.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+3055G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037226 | ||||||
chr14:74037232
|
C | T | 1 | a0004c0004t0004g0117 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.495+3061C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037232 | ||||||
chr14:74037274
|
C | CT | 35 | a0001c0001t0003g0152a0001c0001t0003g0161a0001c0001t0003g0162others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.495+3130dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | |||||
chr14:74037274
|
CT | C | 72 | a0001c0001t0002g0003a0001c0001t0002g0293a0001c0001t0002g0294others(69): Show | 73 | HG00323.hp1 HG00642.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.495+3130delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | |||||
chr14:74037274
|
CTT | C | 9 | a0001c0001t0002g0316a0001c0001t0002g0318a0001c0001t0002g0322others(6): Show | 9 | HG01167.hp1 HG01346.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+3129_495+3130d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | |||||
chr14:74037274
|
CTTTTTTT others(1): Show |
C | 11 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+3123_495+3130d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | |||||
chr14:74037274
|
CTTTTTTT others(3): Show |
C | 12 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+3121_495+3130d others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | |||||
chr14:74037274
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0320 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.495+3120_495+3130d others(13): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | |||||
chr14:74037274
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0308 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.495+3118_495+3130d others(15): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037274 | |||||
chr14:74037326
|
C | T | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.495+3155C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037326 | ||||||
chr14:74037364
|
T | C | 1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.495+3193T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037364 | ||||||
chr14:74037439
|
C | T | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-3126C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037439 | ||||||
chr14:74037459
|
A | AT | 8 | a0003c0003t0001g0033a0003c0003t0001g0190a0003c0003t0001g0191others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-3090dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037459 | |||||
chr14:74037459
|
AT | A | 26 | a0001c0001t0002g0325a0001c0001t0002g0334a0002c0002t0001g0147others(23): Show | 26 | HG00423.hp1 HG01243.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-3090delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74037459 | |||||
chr14:74037629
|
A | G | 4 | a0001c0001t0002g0321a0001c0001t0002g0328a0001c0001t0002g0346others(1): Show | 4 | HG00642.hp2 HG00735.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-2936A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037629 | ||||||
chr14:74037800
|
A | G | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.496-2765A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74037800 | ||||||
chr14:74038021
|
A | ACCACTTA others(1): Show |
285 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(282): Show | 287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.496-2542_496-2541i others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74038021 | |||||
chr14:74038088
|
T | C | 1 | a0002c0002t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.496-2477T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038088 | ||||||
chr14:74038100
|
C | T | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.496-2465C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038100 | ||||||
chr14:74038120
|
G | A | 8 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.496-2445G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038120 | ||||||
chr14:74038225
|
T | A | 81 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(78): Show | 81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.496-2340T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038225 | ||||||
chr14:74038278
|
A | T | 1 | a0001c0001t0002g0338 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.496-2287A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038278 | ||||||
chr14:74038366
|
T | C | 114 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.496-2199T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038366 | ||||||
chr14:74038554
|
T | G | 1 | a0008c0010t0001g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.496-2011T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038554 | ||||||
chr14:74038784
|
G | A | 283 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(280): Show | 285 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.496-1781G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038784 | ||||||
chr14:74038790
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496-1775G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038790 | ||||||
chr14:74038989
|
C | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.496-1576C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038989 | ||||||
chr14:74038989
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.496-1576C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74038989 | ||||||
chr14:74039045
|
C | T | 275 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(272): Show | 277 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.496-1520C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039045 | ||||||
chr14:74039117
|
C | T | 3 | a0005c0006t0006g0194a0005c0006t0006g0195a0005c0006t0006g0196 | 3 | HG03195.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.496-1448C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039117 | ||||||
chr14:74039282
|
A | G | 2 | a0009c0012t0009g0376a0009c0012t0009g0377 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.496-1283A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039282 | ||||||
chr14:74039309
|
A | C | 3 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.496-1256A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039309 | ||||||
chr14:74039392
|
T | A | 81 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(78): Show | 81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.496-1173T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039392 | ||||||
chr14:74039538
|
C | T | 2 | a0005c0006t0001g0134a0005c0006t0001g0135 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.496-1027C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039538 | ||||||
chr14:74039595
|
A | AT | 272 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(269): Show | 274 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.496-956dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74039595 | |||||
chr14:74039624
|
C | T | 1 | a0009c0012t0009g0376 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496-941C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039624 | ||||||
chr14:74039679
|
C | T | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.496-886C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039679 | ||||||
chr14:74039713
|
C | T | 11 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0295others(8): Show | 11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.496-852C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039713 | ||||||
chr14:74039742
|
C | T | 286 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(283): Show | 288 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.496-823C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039742 | ||||||
chr14:74039830
|
C | A | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-735C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74039830 | ||||||
chr14:74040012
|
T | A | 9 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0298others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-553T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040012 | ||||||
chr14:74040060
|
TCA | T | 114 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.496-503_496-502del others(2): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 74040060 | |||||
chr14:74040115
|
C | T | 1 | a0000c0018t0003g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.496-450C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040115 | ||||||
chr14:74040279
|
G | A | 11 | a0002c0002t0001g0207a0002c0002t0001g0248a0002c0002t0001g0249others(8): Show | 11 | HG00280.hp1 HG00735.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-286G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040279 | ||||||
chr14:74040414
|
G | A | 3 | a0004c0009t0007g0138a0004c0009t0007g0139a0004c0009t0007g0140 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.496-151G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 4/11 | chr14 | 74040414 | ||||||
chr14:74040659
|
G | C | 1 | a0003c0003t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.576+14G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74040659 | ||||||
chr14:74040971
|
G | A | 6 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+326G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74040971 | ||||||
chr14:74041004
|
G | A | 6 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+359G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041004 | ||||||
chr14:74041056
|
G | T | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.576+411G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041056 | ||||||
chr14:74041072
|
C | T | 12 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.576+427C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041072 | ||||||
chr14:74041213
|
G | T | 6 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+568G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041213 | ||||||
chr14:74041282
|
G | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.576+637G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041282 | ||||||
chr14:74041465
|
T | G | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.576+820T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041465 | ||||||
chr14:74041480
|
ATAAT | A | 8 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0326others(5): Show | 8 | HG00673.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+839_576+842del others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74041480 | |||||
chr14:74041644
|
C | T | 11 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+999C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041644 | ||||||
chr14:74041756
|
G | A | 11 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.576+1111G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041756 | ||||||
chr14:74041932
|
G | A | 12 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.576+1287G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74041932 | ||||||
chr14:74042037
|
AAAC | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.576+1413_576+1415d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042037 | |||||
chr14:74042090
|
G | A | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.576+1445G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042090 | ||||||
chr14:74042155
|
A | G | 40 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.576+1510A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042155 | ||||||
chr14:74042272
|
C | T | 1 | a0005c0006t0006g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.576+1627C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042272 | ||||||
chr14:74042320
|
G | A | 40 | a0000c0018t0003g0175a0001c0001t0003g0151a0001c0001t0003g0152others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.576+1675G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042320 | ||||||
chr14:74042436
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.576+1791C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042436 | ||||||
chr14:74042535
|
C | T | 1 | a0002c0002t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.576+1890C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042535 | ||||||
chr14:74042563
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.576+1918C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042563 | ||||||
chr14:74042674
|
C | T | 218 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(215): Show | 219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.576+2029C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042674 | ||||||
chr14:74042698
|
C | A | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.576+2053C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042698 | ||||||
chr14:74042716
|
A | G | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.576+2071A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042716 | ||||||
chr14:74042837
|
C | T | 1 | a0003c0003t0001g0023 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.576+2192C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042837 | ||||||
chr14:74042859
|
C | G | 1 | a0001c0001t0002g0366 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.576+2214C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042859 | ||||||
chr14:74042871
|
CACACACA others(1): Show |
C | 5 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+2234_576+2241d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042871 | |||||
chr14:74042873
|
CACACAG | C | 6 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0008g0378others(3): Show | 6 | HG02451.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+2234_576+2239d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042873 | |||||
chr14:74042879
|
G | GAC | 89 | a0001c0001t0003g0182a0001c0001t0003g0185a0001c0001t0003g0274others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.576+2265_576+2266d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042879
|
G | GACAC | 12 | a0001c0001t0003g0156a0002c0002t0001g0198a0002c0002t0001g0199others(9): Show | 12 | HG01074.hp2 HG01934.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.576+2263_576+2266d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042879
|
G | GACACAC | 39 | a0002c0002t0001g0202a0003c0003t0001g0042a0003c0003t0001g0065others(36): Show | 40 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.576+2261_576+2266d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042879
|
G | GACACACA others(1): Show |
6 | a0004c0004t0004g0095a0004c0004t0004g0114a0004c0004t0004g0126others(3): Show | 6 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+2259_576+2266d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042879
|
GAC | G | 46 | a0000c0018t0003g0175a0001c0001t0002g0305a0001c0001t0003g0151others(43): Show | 46 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.576+2265_576+2266d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042879
|
GACAC | G | 76 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(73): Show | 77 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.576+2263_576+2266d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042879
|
GACACAC | G | 13 | a0001c0001t0003g0150a0001c0001t0003g0295a0003c0003t0003g0189others(10): Show | 13 | HG01243.hp1 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.576+2261_576+2266d others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042879
|
GACACACA others(1): Show |
G | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.576+2259_576+2266d others(10): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74042879 | |||||
chr14:74042887
|
C | G | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.576+2242C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042887 | ||||||
chr14:74042889
|
C | G | 4 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+2244C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042889 | ||||||
chr14:74042891
|
C | G | 5 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+2246C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042891 | ||||||
chr14:74042895
|
C | G | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.576+2250C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042895 | ||||||
chr14:74042957
|
A | G | 230 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(227): Show | 231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.576+2312A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74042957 | ||||||
chr14:74043187
|
T | C | 1 | a0003c0003t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.576+2542T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043187 | ||||||
chr14:74043208
|
A | G | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.576+2563A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043208 | ||||||
chr14:74043245
|
A | G | 1 | a0004c0004t0004g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.576+2600A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043245 | ||||||
chr14:74043249
|
A | G | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+2604A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043249 | ||||||
chr14:74043253
|
T | A | 1 | a0002c0002t0001g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.576+2608T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043253 | ||||||
chr14:74043269
|
G | T | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.576+2624G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043269 | ||||||
chr14:74043273
|
A | G | 285 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(282): Show | 287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.576+2628A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043273 | ||||||
chr14:74043279
|
G | A | 1 | a0006c0005t0003g0375 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.576+2634G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043279 | ||||||
chr14:74043302
|
G | C | 1 | a0003c0003t0001g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.576+2657G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043302 | ||||||
chr14:74043533
|
G | A | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.577-2527G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043533 | ||||||
chr14:74043543
|
C | T | 5 | a0002c0002t0001g0197a0003c0003t0001g0047a0003c0003t0001g0068others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-2517C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043543 | ||||||
chr14:74043551
|
C | T | 4 | a0006c0005t0003g0374a0006c0005t0003g0375a0009c0012t0009g0376others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-2509C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043551 | ||||||
chr14:74043556
|
C | CA | 76 | a0000c0018t0003g0175a0001c0001t0002g0352a0001c0001t0003g0150others(73): Show | 78 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.577-2476dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | |||||
chr14:74043556
|
CA | C | 65 | a0001c0001t0002g0003a0001c0001t0002g0293a0001c0001t0002g0306others(62): Show | 66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.577-2476delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | |||||
chr14:74043556
|
CAA | C | 73 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(70): Show | 73 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.577-2477_577-2476d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | |||||
chr14:74043556
|
CAAA | C | 10 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(7): Show | 10 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-2478_577-2476d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74043556 | |||||
chr14:74043557
|
A | C | 3 | a0004c0004t0004g0089a0004c0004t0004g0114a0004c0004t0004g0119 | 3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.577-2503A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043557 | ||||||
chr14:74043587
|
C | G | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.577-2473C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043587 | ||||||
chr14:74043666
|
C | A | 1 | a0003c0003t0001g0052 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.577-2394C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043666 | ||||||
chr14:74043776
|
G | T | 1 | a0002c0002t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.577-2284G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043776 | ||||||
chr14:74043784
|
C | T | 1 | a0003c0003t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.577-2276C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043784 | ||||||
chr14:74043881
|
T | G | 2 | a0009c0012t0009g0376a0009c0012t0009g0377 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.577-2179T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043881 | ||||||
chr14:74043905
|
T | C | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-2155T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043905 | ||||||
chr14:74043909
|
G | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.577-2151G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74043909 | ||||||
chr14:74044021
|
G | A | 10 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(7): Show | 10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-2039G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044021 | ||||||
chr14:74044170
|
C | T | 6 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-1890C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044170 | ||||||
chr14:74044180
|
A | C | 1 | a0002c0002t0001g0266 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.577-1880A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044180 | ||||||
chr14:74044193
|
C | T | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.577-1867C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044193 | ||||||
chr14:74044195
|
G | A | 1 | a0000c0018t0003g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.577-1865G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044195 | ||||||
chr14:74044239
|
CTGTCTCA others(17): Show |
C | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.577-1819_577-1796d others(26): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044239 | |||||
chr14:74044260
|
A | AAAAT | 4 | a0001c0001t0002g0320a0004c0007t0003g0361a0004c0007t0003g0364others(1): Show | 4 | HG01069.hp1 HG02145.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-1781_577-1778d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044260 | |||||
chr14:74044403
|
A | T | 1 | a0001c0001t0002g0346 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.577-1657A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044403 | ||||||
chr14:74044421
|
C | G | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.577-1639C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044421 | ||||||
chr14:74044475
|
C | CT | 224 | a0000c0018t0003g0175a0001c0001t0002g0318a0001c0001t0002g0322others(221): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.577-1569dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044475 | |||||
chr14:74044475
|
C | CTT | 129 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(126): Show | 130 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.577-1570_577-1569d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74044475 | |||||
chr14:74044476
|
T | TC | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-1584_577-1583i others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044476 | ||||||
chr14:74044508
|
G | A | 21 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(18): Show | 21 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.577-1552G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044508 | ||||||
chr14:74044523
|
C | T | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.577-1537C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044523 | ||||||
chr14:74044651
|
C | T | 4 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-1409C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044651 | ||||||
chr14:74044704
|
T | C | 1 | a0004c0004t0004g0092 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.577-1356T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044704 | ||||||
chr14:74044762
|
C | G | 3 | a0001c0001t0003g0184a0001c0001t0003g0186a0001c0001t0003g0187 | 3 | HG02615.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.577-1298C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044762 | ||||||
chr14:74044869
|
G | A | 21 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(18): Show | 21 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.577-1191G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74044869 | ||||||
chr14:74045030
|
G | A | 1 | a0001c0001t0003g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.577-1030G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045030 | ||||||
chr14:74045087
|
C | G | 4 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-973C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045087 | ||||||
chr14:74045127
|
A | G | 1 | a0004c0007t0003g0365 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.577-933A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045127 | ||||||
chr14:74045172
|
T | C | 1 | a0009c0012t0009g0376 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.577-888T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045172 | ||||||
chr14:74045175
|
T | C | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.577-885T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045175 | ||||||
chr14:74045232
|
A | G | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-828A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045232 | ||||||
chr14:74045302
|
A | ATTCTT | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.577-756_577-755ins others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 74045302 | |||||
chr14:74045371
|
G | A | 46 | a0002c0002t0001g0209a0004c0004t0004g0002a0004c0004t0004g0087others(43): Show | 47 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.577-689G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045371 | ||||||
chr14:74045496
|
C | A | 230 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(227): Show | 231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.577-564C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045496 | ||||||
chr14:74045686
|
T | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.577-374T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045686 | ||||||
chr14:74045995
|
T | C | 285 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(282): Show | 287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.577-65T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 5/11 | chr14 | 74045995 | ||||||
chr14:74046218
|
C | G | 1 | a0007c0008t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.647+88C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046218 | ||||||
chr14:74046402
|
CATCCAGG others(2): Show |
C | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.647+282_647+290del others(9): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74046402 | |||||
chr14:74046530
|
A | T | 8 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.647+400A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046530 | ||||||
chr14:74046533
|
T | C | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.647+403T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046533 | ||||||
chr14:74046543
|
T | C | 1 | a0001c0001t0002g0330 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.647+413T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046543 | ||||||
chr14:74046643
|
G | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+513G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046643 | ||||||
chr14:74046644
|
A | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+514A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046644 | ||||||
chr14:74046647
|
A | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+517A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046647 | ||||||
chr14:74046648
|
T | C | 1 | a0003c0003t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.647+518T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046648 | ||||||
chr14:74046849
|
C | T | 2 | a0003c0003t0001g0190a0003c0003t0001g0191 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.647+719C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046849 | ||||||
chr14:74046937
|
G | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.647+807G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046937 | ||||||
chr14:74046939
|
G | A | 1 | a0003c0003t0001g0012 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.647+809G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74046939 | ||||||
chr14:74047407
|
C | CTTTA | 112 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(109): Show | 112 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.648-487_648-484dup others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | |||||
chr14:74047407
|
C | CTTTATTT others(1): Show |
29 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201others(26): Show | 29 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.648-491_648-484dup others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | |||||
chr14:74047407
|
C | CTTTATTT others(5): Show |
13 | a0002c0002t0001g0198a0002c0002t0001g0224a0002c0002t0001g0225others(10): Show | 13 | HG02258.hp1 HG02486.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.648-495_648-484dup others(12): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | |||||
chr14:74047407
|
C | CTTTATTT others(9): Show |
1 | a0002c0002t0001g0223 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.648-499_648-484dup others(16): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | |||||
chr14:74047407
|
C | CTTTATTT others(13): Show |
1 | a0003c0003t0001g0078 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.648-503_648-484dup others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | |||||
chr14:74047407
|
CTTTA | C | 13 | a0002c0002t0001g0147a0002c0002t0001g0148a0002c0002t0001g0192others(10): Show | 13 | HG00558.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.648-487_648-484del others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047407 | |||||
chr14:74047413
|
T | TTATG | 34 | a0000c0018t0003g0175a0001c0001t0002g0321a0001c0001t0002g0328others(31): Show | 34 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.648-514_648-513ins others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 74047413 | |||||
chr14:74047417
|
T | G | 79 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(76): Show | 80 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.648-513T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047417 | ||||||
chr14:74047463
|
C | G | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.648-467C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047463 | ||||||
chr14:74047594
|
C | T | 1 | a0002c0002t0001g0210 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.648-336C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047594 | ||||||
chr14:74047595
|
G | A | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.648-335G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047595 | ||||||
chr14:74047685
|
C | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.648-245C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047685 | ||||||
chr14:74047899
|
C | A | 1 | a0002c0002t0001g0266 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.648-31C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 6/11 | chr14 | 74047899 | ||||||
chr14:74048152
|
A | G | 1 | a0001c0001t0002g0309 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.792+78A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048152 | ||||||
chr14:74048180
|
A | T | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.792+106A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048180 | ||||||
chr14:74048375
|
T | G | 2 | a0002c0002t0001g0244a0002c0002t0001g0289 | 2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.792+301T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048375 | ||||||
chr14:74048380
|
C | T | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.792+306C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048380 | ||||||
chr14:74048881
|
G | T | 2 | a0002c0002t0001g0269a0003c0003t0001g0066 | 2 | NA18984.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.792+807G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048881 | ||||||
chr14:74048951
|
C | T | 1 | a0002c0002t0001g0220 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.793-751C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048951 | ||||||
chr14:74048957
|
T | C | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.793-745T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74048957 | ||||||
chr14:74049018
|
A | C | 7 | a0002c0002t0001g0214a0002c0002t0001g0239a0002c0002t0001g0240others(4): Show | 7 | HG00639.hp2 HG01261.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-684A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049018 | ||||||
chr14:74049030
|
G | A | 1 | a0003c0003t0001g0069 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.793-672G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049030 | ||||||
chr14:74049120
|
C | A | 1 | a0002c0002t0001g0368 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.793-582C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049120 | ||||||
chr14:74049208
|
T | C | 10 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(7): Show | 10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-494T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049208 | ||||||
chr14:74049364
|
A | G | 2 | a0001c0001t0003g0301a0001c0001t0003g0303 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.793-338A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049364 | ||||||
chr14:74049379
|
T | TA | 281 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(278): Show | 283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.793-313dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 74049379 | |||||
chr14:74049535
|
A | C | 1 | a0006c0005t0008g0380 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.793-167A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049535 | ||||||
chr14:74049640
|
C | T | 1 | a0013c0017t0001g0351 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.793-62C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 7/11 | chr14 | 74049640 | ||||||
chr14:74050209
|
TTTA | T | 5 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+22_1286+24del others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74050209 | |||||
chr14:74050309
|
G | T | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+114G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050309 | ||||||
chr14:74050403
|
C | T | 8 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+208C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050403 | ||||||
chr14:74050451
|
T | C | 8 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+256T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050451 | ||||||
chr14:74050529
|
T | A | 3 | a0002c0002t0001g0249a0002c0002t0001g0250a0002c0002t0001g0268 | 3 | HG00280.hp1 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1286+334T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050529 | ||||||
chr14:74050535
|
A | G | 3 | a0001c0001t0003g0165a0001c0001t0003g0173a0001c0001t0003g0179 | 3 | HG04115.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1286+340A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050535 | ||||||
chr14:74050543
|
C | A | 1 | a0004c0004t0004g0103 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1286+348C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050543 | ||||||
chr14:74050584
|
A | G | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1286+389A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050584 | ||||||
chr14:74050674
|
C | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1286+479C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74050674 | ||||||
chr14:74051042
|
G | A | 21 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(18): Show | 21 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+847G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051042 | ||||||
chr14:74051070
|
C | T | 1 | a0001c0001t0002g0338 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1286+875C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051070 | ||||||
chr14:74051116
|
T | C | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1286+921T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051116 | ||||||
chr14:74051117
|
T | A | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1286+922T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051117 | ||||||
chr14:74051137
|
GGGAGGCT others(1394): Show |
G | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1286+965_1286+2365 others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74051137 | |||||
chr14:74051201
|
G | A | 8 | a0002c0002t0001g0223a0002c0002t0001g0224a0002c0002t0001g0225others(5): Show | 8 | HG02155.hp1 NA18612.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+1006G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051201 | ||||||
chr14:74051215
|
G | C | 132 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(129): Show | 133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1286+1020G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051215 | ||||||
chr14:74051327
|
C | T | 5 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+1132C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051327 | ||||||
chr14:74051365
|
A | T | 1 | a0003c0003t0001g0056 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1286+1170A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051365 | ||||||
chr14:74051370
|
A | G | 132 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(129): Show | 133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1286+1175A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051370 | ||||||
chr14:74051394
|
C | T | 1 | a0002c0002t0001g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1286+1199C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74051394 | ||||||
chr14:74052174
|
C | T | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1286+1979C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052174 | ||||||
chr14:74052357
|
C | A | 2 | a0001c0001t0003g0301a0001c0001t0003g0303 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1286+2162C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052357 | ||||||
chr14:74052644
|
C | CA | 19 | a0001c0001t0003g0188a0003c0003t0001g0052a0004c0007t0003g0004others(16): Show | 19 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1286+2462dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74052644 | |||||
chr14:74052860
|
C | T | 2 | a0002c0002t0001g0255a0002c0002t0001g0269 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1286+2665C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052860 | ||||||
chr14:74052877
|
G | T | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+2682G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74052877 | ||||||
chr14:74052934
|
AGGCTGCA others(9): Show |
A | 375 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(372): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1287-2616_1287-260 others(20): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74052934 | |||||
chr14:74053035
|
A | T | 3 | a0007c0008t0001g0213a0007c0008t0001g0216a0007c0008t0001g0273 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1287-2549A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053035 | ||||||
chr14:74053056
|
T | C | 25 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0001g0210others(22): Show | 25 | HG01070.hp1 HG01074.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1287-2528T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053056 | ||||||
chr14:74053121
|
A | T | 2 | a0002c0002t0001g0199a0002c0002t0001g0201 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1287-2463A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053121 | ||||||
chr14:74053125
|
T | A | 12 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-2459T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053125 | ||||||
chr14:74053161
|
C | A | 1 | a0004c0004t0004g0118 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1287-2423C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053161 | ||||||
chr14:74053222
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1287-2362C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053222 | ||||||
chr14:74053273
|
C | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-2311C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053273 | ||||||
chr14:74053373
|
A | C | 9 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0298others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287-2211A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053373 | ||||||
chr14:74053390
|
T | C | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1287-2194T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053390 | ||||||
chr14:74053607
|
A | G | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1287-1977A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053607 | ||||||
chr14:74053957
|
A | C | 229 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(226): Show | 230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1287-1627A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74053957 | ||||||
chr14:74054036
|
G | A | 113 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(110): Show | 114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1287-1548G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054036 | ||||||
chr14:74054037
|
G | C | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-1547G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054037 | ||||||
chr14:74054127
|
C | T | 63 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1287-1457C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054127 | ||||||
chr14:74054168
|
G | A | 63 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1287-1416G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054168 | ||||||
chr14:74054212
|
A | G | 229 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(226): Show | 230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1287-1372A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054212 | ||||||
chr14:74054305
|
T | C | 134 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(131): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1287-1279T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054305 | ||||||
chr14:74054385
|
G | GT | 8 | a0002c0002t0001g0215a0002c0002t0001g0220a0002c0002t0001g0234others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1287-1188dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054385 | |||||
chr14:74054385
|
G | T | 1 | a0003c0003t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1287-1199G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054385 | ||||||
chr14:74054410
|
G | A | 1 | a0002c0002t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1287-1174G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054410 | ||||||
chr14:74054415
|
G | C | 1 | a0001c0001t0003g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1287-1169G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054415 | ||||||
chr14:74054430
|
G | A | 83 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1287-1154G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054430 | ||||||
chr14:74054441
|
C | T | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-1143C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054441 | ||||||
chr14:74054442
|
G | T | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1287-1142G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054442 | ||||||
chr14:74054634
|
C | T | 2 | a0001c0001t0002g0358a0001c0001t0002g0360 | 2 | NA18983.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1287-950C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054634 | ||||||
chr14:74054652
|
C | T | 1 | a0006c0005t0016g0381 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1287-932C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054652 | ||||||
chr14:74054678
|
C | CT | 195 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(192): Show | 196 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1287-889dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054678 | |||||
chr14:74054678
|
C | CTT | 9 | a0003c0003t0001g0080a0003c0003t0003g0189a0005c0006t0001g0131others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-890_1287-889d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054678 | |||||
chr14:74054678
|
CT | C | 12 | a0002c0002t0001g0203a0002c0002t0001g0214a0002c0002t0001g0242others(9): Show | 12 | HG00323.hp1 HG01123.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-889delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74054678 | |||||
chr14:74054747
|
G | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-837G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054747 | ||||||
chr14:74054867
|
C | T | 2 | a0003c0003t0001g0064a0003c0003t0001g0382 | 2 | HG02027.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1287-717C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054867 | ||||||
chr14:74054870
|
C | T | 1 | a0002c0002t0001g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1287-714C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054870 | ||||||
chr14:74054899
|
G | A | 3 | a0001c0001t0002g0334a0001c0001t0002g0335a0002c0002t0001g0269 | 3 | NA18953.hp2 NA18960.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1287-685G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74054899 | ||||||
chr14:74055106
|
T | C | 1 | a0002c0002t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1287-478T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055106 | ||||||
chr14:74055154
|
C | CT | 8 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(5): Show | 8 | HG01081.hp1 HG01884.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1287-419dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 74055154 | |||||
chr14:74055170
|
C | T | 113 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(110): Show | 114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1287-414C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055170 | ||||||
chr14:74055171
|
G | A | 1 | a0004c0007t0003g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1287-413G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055171 | ||||||
chr14:74055211
|
C | T | 39 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0153others(36): Show | 39 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1287-373C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055211 | ||||||
chr14:74055212
|
G | A | 1 | a0003c0003t0001g0045 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1287-372G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055212 | ||||||
chr14:74055220
|
C | G | 3 | a0004c0009t0007g0138a0004c0009t0007g0139a0004c0009t0007g0140 | 3 | HG02572.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1287-364C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055220 | ||||||
chr14:74055276
|
G | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1287-308G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055276 | ||||||
chr14:74055340
|
G | C | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1287-244G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055340 | ||||||
chr14:74055401
|
G | A | 3 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1287-183G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055401 | ||||||
chr14:74055539
|
A | G | 1 | a0008c0010t0001g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1287-45A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055539 | ||||||
chr14:74055549
|
T | C | 2 | a0002c0002t0001g0211a0002c0002t0001g0212 | 2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1287-35T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 8/11 | chr14 | 74055549 | ||||||
chr14:74055785
|
G | A | 2 | a0009c0012t0009g0376a0009c0012t0009g0377 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1388+100G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74055785 | ||||||
chr14:74056033
|
T | TA | 3 | a0004c0004t0004g0090a0004c0004t0004g0103a0004c0004t0004g0122 | 3 | HG01123.hp1 HG02300.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1388+349dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056033 | |||||
chr14:74056034
|
AT | A | 129 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(126): Show | 130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1388+364delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056034 | |||||
chr14:74056035
|
T | A | 144 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(141): Show | 145 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1388+350T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056035 | ||||||
chr14:74056036
|
T | A | 127 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(124): Show | 128 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1388+351T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056036 | ||||||
chr14:74056192
|
C | T | 113 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(110): Show | 114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1388+507C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056192 | ||||||
chr14:74056198
|
A | AT | 115 | a0001c0001t0002g0003a0001c0001t0002g0293a0001c0001t0002g0294others(112): Show | 117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1388+533dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | |||||
chr14:74056198
|
A | ATT | 45 | a0001c0001t0002g0292a0001c0001t0002g0329a0001c0001t0002g0330others(42): Show | 45 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1388+532_1388+533d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | |||||
chr14:74056198
|
A | ATTT | 77 | a0001c0001t0003g0168a0001c0001t0003g0172a0001c0001t0003g0178others(74): Show | 77 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1388+531_1388+533d others(5): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | |||||
chr14:74056198
|
A | ATTTT | 13 | a0003c0003t0001g0014a0003c0003t0001g0015a0003c0003t0001g0016others(10): Show | 13 | HG02135.hp1 HG02895.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.1388+530_1388+533d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056198 | |||||
chr14:74056322
|
C | G | 1 | a0001c0001t0003g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1389-584C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056322 | ||||||
chr14:74056324
|
C | T | 10 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(7): Show | 10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1389-582C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056324 | ||||||
chr14:74056344
|
G | C | 229 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(226): Show | 230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1389-562G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056344 | ||||||
chr14:74056380
|
T | G | 1 | a0002c0002t0001g0290 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1389-526T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056380 | ||||||
chr14:74056397
|
A | G | 8 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1389-509A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056397 | ||||||
chr14:74056474
|
ACAGG | A | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1389-429_1389-426d others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056474 | |||||
chr14:74056752
|
G | C | 1 | a0002c0002t0001g0252 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1389-154G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056752 | ||||||
chr14:74056816
|
TA | T | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389-81delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 74056816 | |||||
chr14:74056836
|
A | G | 1 | a0006c0005t0016g0381 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1389-70A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 9/11 | chr14 | 74056836 | ||||||
chr14:74057022
|
C | T | 1 | a0002c0002t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1463+42C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 10/11 | chr14 | 74057022 | ||||||
chr14:74057091
|
G | C | 1 | a0001c0001t0002g0305 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1464-53G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 10/11 | chr14 | 74057091 | ||||||
chr14:74057295
|
T | C | 12 | a0003c0003t0001g0015a0003c0003t0001g0020a0003c0003t0001g0021others(9): Show | 12 | HG00423.hp2 HG02165.hp1 NA18975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1578+37T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057295 | ||||||
chr14:74057454
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1578+196T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057454 | ||||||
chr14:74057490
|
G | C | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1578+232G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057490 | ||||||
chr14:74057495
|
C | T | 3 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1578+237C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057495 | ||||||
chr14:74057648
|
T | G | 10 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(7): Show | 10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1578+390T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057648 | ||||||
chr14:74057826
|
A | G | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1578+568A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057826 | ||||||
chr14:74057962
|
T | C | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+704T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057962 | ||||||
chr14:74057990
|
G | A | 5 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0146others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+732G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74057990 | ||||||
chr14:74058125
|
A | G | 6 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+867A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058125 | ||||||
chr14:74058151
|
C | A | 1 | a0008c0010t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1578+893C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058151 | ||||||
chr14:74058235
|
G | A | 2 | a0006c0005t0003g0374a0006c0005t0003g0375 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1578+977G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058235 | ||||||
chr14:74058281
|
C | T | 8 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1578+1023C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058281 | ||||||
chr14:74058289
|
T | C | 1 | a0002c0002t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1578+1031T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058289 | ||||||
chr14:74058290
|
G | A | 4 | a0002c0002t0001g0147a0002c0002t0001g0148a0002c0002t0001g0192others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+1032G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058290 | ||||||
chr14:74058318
|
C | A | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1578+1060C>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058318 | ||||||
chr14:74058340
|
ACAACAAC others(19): Show |
A | 10 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(7): Show | 10 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1578+1083_1578+110 others(30): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058340 | ||||||
chr14:74058344
|
C | T | 1 | a0002c0002t0001g0272 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1578+1086C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058344 | ||||||
chr14:74058448
|
G | GA | 173 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(170): Show | 175 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1578+1206dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74058448 | |||||
chr14:74058448
|
GA | G | 16 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(13): Show | 16 | HG02258.hp1 HG02280.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1578+1206delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74058448 | |||||
chr14:74058485
|
G | A | 2 | a0004c0009t0007g0138a0004c0009t0007g0140 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1578+1227G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058485 | ||||||
chr14:74058596
|
C | CT | 135 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1578+1350dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74058596 | |||||
chr14:74058708
|
A | G | 134 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(131): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1578+1450A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058708 | ||||||
chr14:74058738
|
C | G | 1 | a0003c0003t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1578+1480C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058738 | ||||||
chr14:74058822
|
C | T | 2 | a0001c0001t0003g0301a0001c0001t0003g0303 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1578+1564C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058822 | ||||||
chr14:74058952
|
C | T | 1 | a0003c0003t0001g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1578+1694C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74058952 | ||||||
chr14:74059019
|
G | A | 8 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1578+1761G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059019 | ||||||
chr14:74059057
|
C | G | 1 | a0002c0002t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1578+1799C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059057 | ||||||
chr14:74059083
|
T | TCAAAAAA others(3): Show |
1 | a0003c0003t0001g0058 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1578+1826_1578+183 others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74059083 | |||||
chr14:74059083
|
TC | T | 9 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0298others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578+1826delC | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059083 | ||||||
chr14:74059084
|
C | CA | 33 | a0001c0001t0002g0292a0001c0001t0002g0307a0001c0001t0002g0357others(30): Show | 33 | HG01255.hp2 HG02055.hp2 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.1578+1848dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74059084 | |||||
chr14:74059084
|
CA | C | 59 | a0001c0001t0002g0315a0001c0001t0003g0156a0001c0001t0003g0274others(56): Show | 60 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.1578+1848delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74059084 | |||||
chr14:74059085
|
A | T | 9 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0298others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578+1827A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059085 | ||||||
chr14:74059128
|
T | C | 4 | a0001c0001t0003g0156a0001c0001t0003g0185a0001c0001t0003g0274others(1): Show | 4 | HG01074.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+1870T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059128 | ||||||
chr14:74059187
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1578+1929G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059187 | ||||||
chr14:74059461
|
C | T | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1578+2203C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059461 | ||||||
chr14:74059485
|
C | G | 134 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(131): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1578+2227C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059485 | ||||||
chr14:74059494
|
G | A | 134 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(131): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1578+2236G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059494 | ||||||
chr14:74059610
|
G | A | 11 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1578+2352G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059610 | ||||||
chr14:74059626
|
C | T | 4 | a0005c0006t0006g0193a0005c0006t0006g0194a0005c0006t0006g0195others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+2368C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059626 | ||||||
chr14:74059627
|
G | A | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578+2369G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059627 | ||||||
chr14:74059636
|
G | A | 6 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+2378G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059636 | ||||||
chr14:74059662
|
T | C | 4 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+2404T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059662 | ||||||
chr14:74059950
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1578+2692T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74059950 | ||||||
chr14:74060000
|
G | A | 63 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1578+2742G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060000 | ||||||
chr14:74060075
|
G | A | 8 | a0004c0004t0004g0088a0004c0004t0004g0098a0004c0004t0004g0110others(5): Show | 8 | NA18967.hp2 NA18972.hp2 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578+2817G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060075 | ||||||
chr14:74060148
|
T | A | 64 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1578+2890T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060148 | ||||||
chr14:74060209
|
G | A | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1578+2951G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060209 | ||||||
chr14:74060239
|
A | G | 142 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(139): Show | 143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1578+2981A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060239 | ||||||
chr14:74060292
|
G | C | 1 | a0009c0012t0009g0376 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1578+3034G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060292 | ||||||
chr14:74060333
|
C | T | 2 | a0008c0010t0001g0041a0008c0010t0001g0055 | 2 | HG02015.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1578+3075C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060333 | ||||||
chr14:74060487
|
A | G | 113 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(110): Show | 114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1578+3229A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060487 | ||||||
chr14:74060500
|
G | A | 378 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(375): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1578+3242G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060500 | ||||||
chr14:74060646
|
C | T | 2 | a0001c0001t0002g0315a0001c0001t0002g0316 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1578+3388C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060646 | ||||||
chr14:74060811
|
CT | C | 5 | a0006c0005t0005g0369a0006c0005t0005g0370a0006c0005t0005g0371others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+3557delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74060811 | |||||
chr14:74060923
|
C | T | 1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1578+3665C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060923 | ||||||
chr14:74060924
|
T | C | 8 | a0002c0002t0001g0223a0002c0002t0001g0224a0002c0002t0001g0225others(5): Show | 8 | HG02155.hp1 NA18612.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1578+3666T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74060924 | ||||||
chr14:74061001
|
G | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1579-3687G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061001 | ||||||
chr14:74061294
|
C | CATTT | 66 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(63): Show | 67 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1579-3373_1579-337 others(8): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74061294 | |||||
chr14:74061320
|
G | T | 134 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(131): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1579-3368G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061320 | ||||||
chr14:74061321
|
A | T | 134 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(131): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1579-3367A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061321 | ||||||
chr14:74061499
|
T | C | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1579-3189T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061499 | ||||||
chr14:74061585
|
CAA | C | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1579-3101_1579-310 others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74061585 | |||||
chr14:74061643
|
T | C | 1 | a0002c0002t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1579-3045T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061643 | ||||||
chr14:74061681
|
A | G | 1 | a0001c0001t0003g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1579-3007A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061681 | ||||||
chr14:74061785
|
A | C | 1 | a0008c0010t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1579-2903A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061785 | ||||||
chr14:74061802
|
A | T | 2 | a0001c0001t0002g0328a0001c0001t0002g0347 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1579-2886A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74061802 | ||||||
chr14:74062024
|
A | G | 7 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0006others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-2664A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062024 | ||||||
chr14:74062048
|
T | TG | 12 | a0002c0002t0001g0231a0002c0002t0001g0264a0003c0003t0001g0011others(9): Show | 12 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579-2637dupG | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062048 | |||||
chr14:74062051
|
G | GA | 89 | a0001c0001t0002g0003a0001c0001t0002g0294a0001c0001t0002g0306others(86): Show | 90 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1579-2608dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
G | GAA | 33 | a0001c0001t0002g0293a0001c0001t0002g0297a0001c0001t0002g0305others(30): Show | 33 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1579-2609_1579-260 others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
G | GAAA | 8 | a0001c0001t0002g0292a0001c0001t0002g0352a0001c0001t0003g0165others(5): Show | 8 | HG02135.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1579-2610_1579-260 others(7): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
GA | G | 20 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(17): Show | 20 | HG01081.hp1 HG02040.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.1579-2608delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
GAA | G | 47 | a0003c0003t0003g0189a0004c0004t0004g0002a0004c0004t0004g0088others(44): Show | 48 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1579-2609_1579-260 others(6): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
GAAAAA | G | 8 | a0006c0005t0003g0374a0006c0005t0003g0375a0006c0005t0005g0369others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1579-2612_1579-260 others(9): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0002g0315a0001c0001t0002g0316 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1579-2617_1579-260 others(14): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
GAAAAAAA others(5): Show |
G | 3 | a0001c0001t0003g0167a0004c0007t0003g0006a0004c0009t0007g0139 | 3 | HG02809.hp2 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1579-2619_1579-260 others(16): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062051
|
GAAAAAAA others(6): Show |
G | 8 | a0004c0007t0003g0004a0004c0007t0003g0005a0004c0007t0003g0007others(5): Show | 8 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1579-2620_1579-260 others(17): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062051 | |||||
chr14:74062052
|
A | G | 74 | a0002c0002t0001g0237a0002c0002t0001g0270a0003c0003t0001g0008others(71): Show | 74 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1579-2636A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062052 | ||||||
chr14:74062053
|
A | G | 6 | a0003c0015t0001g0059a0005c0006t0001g0136a0005c0006t0001g0137others(3): Show | 6 | HG02486.hp1 HG03195.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-2635A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062053 | ||||||
chr14:74062054
|
A | G | 5 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0133others(2): Show | 5 | HG01243.hp1 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-2634A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062054 | ||||||
chr14:74062055
|
A | G | 1 | a0005c0006t0001g0132 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1579-2633A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062055 | ||||||
chr14:74062150
|
A | T | 274 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(271): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1579-2538A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062150 | ||||||
chr14:74062167
|
A | G | 1 | a0002c0016t0001g0218 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1579-2521A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062167 | ||||||
chr14:74062192
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1579-2496C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062192 | ||||||
chr14:74062205
|
T | A | 1 | a0003c0003t0015g0027 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1579-2483T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062205 | ||||||
chr14:74062206
|
A | T | 1 | a0003c0003t0015g0027 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1579-2482A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062206 | ||||||
chr14:74062207
|
A | T | 1 | a0006c0005t0003g0374 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1579-2481A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062207 | ||||||
chr14:74062249
|
G | C | 50 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0151others(47): Show | 50 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1579-2439G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062249 | ||||||
chr14:74062329
|
C | T | 1 | a0002c0002t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1579-2359C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062329 | ||||||
chr14:74062333
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1579-2355G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062333 | ||||||
chr14:74062730
|
A | G | 63 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1579-1958A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062730 | ||||||
chr14:74062776
|
C | T | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1579-1912C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062776 | ||||||
chr14:74062780
|
C | T | 2 | a0004c0009t0007g0138a0004c0009t0007g0140 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1579-1908C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062780 | ||||||
chr14:74062797
|
T | C | 274 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(271): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1579-1891T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062797 | ||||||
chr14:74062808
|
GA | G | 45 | a0004c0004t0004g0002a0004c0004t0004g0087a0004c0004t0004g0088others(42): Show | 46 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1579-1870delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74062808 | |||||
chr14:74062820
|
C | T | 134 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(131): Show | 135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1579-1868C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062820 | ||||||
chr14:74062832
|
G | C | 1 | a0002c0002t0014g0238 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1579-1856G>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062832 | ||||||
chr14:74062871
|
A | C | 1 | a0011c0013t0001g0017 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1579-1817A>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062871 | ||||||
chr14:74062957
|
T | G | 296 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(293): Show | 298 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1579-1731T>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062957 | ||||||
chr14:74062979
|
A | G | 3 | a0006c0005t0008g0378a0006c0005t0008g0379a0006c0005t0008g0380 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1579-1709A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062979 | ||||||
chr14:74062983
|
C | T | 3 | a0003c0003t0001g0022a0003c0003t0001g0048a0003c0015t0001g0059 | 3 | HG02083.hp1 NA18957.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1579-1705C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74062983 | ||||||
chr14:74063122
|
G | T | 2 | a0003c0003t0003g0189a0005c0006t0001g0137 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1579-1566G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063122 | ||||||
chr14:74063156
|
C | T | 2 | a0003c0003t0001g0037a0003c0003t0001g0060 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1579-1532C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063156 | ||||||
chr14:74063164
|
C | T | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-1524C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063164 | ||||||
chr14:74063165
|
C | T | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1579-1523C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063165 | ||||||
chr14:74063190
|
C | CT | 45 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0153others(42): Show | 45 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1579-1484dupT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063190 | |||||
chr14:74063190
|
CT | C | 49 | a0001c0001t0002g0319a0003c0003t0001g0012a0003c0003t0001g0056others(46): Show | 50 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1579-1484delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063190 | |||||
chr14:74063272
|
C | T | 1 | a0002c0002t0001g0252 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1579-1416C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063272 | ||||||
chr14:74063316
|
A | G | 1 | a0013c0017t0001g0351 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1579-1372A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063316 | ||||||
chr14:74063327
|
T | C | 274 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0293others(271): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1579-1361T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063327 | ||||||
chr14:74063464
|
C | T | 4 | a0002c0002t0001g0147a0002c0002t0001g0148a0002c0002t0001g0192others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1579-1224C>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063464 | ||||||
chr14:74063593
|
T | C | 114 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1579-1095T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063593 | ||||||
chr14:74063723
|
A | G | 281 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(278): Show | 283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1579-965A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063723 | ||||||
chr14:74063829
|
G | T | 1 | a0001c0001t0003g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1579-859G>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74063829 | ||||||
chr14:74063865
|
CA | C | 263 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(260): Show | 265 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.1579-807delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063865 | |||||
chr14:74063865
|
CAA | C | 9 | a0001c0001t0002g0316a0001c0001t0002g0326a0001c0001t0002g0354others(6): Show | 9 | HG01167.hp1 HG01167.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579-808_1579-807d others(4): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74063865 | |||||
chr14:74064011
|
T | A | 95 | a0003c0003t0001g0008a0003c0003t0001g0009a0003c0003t0001g0010others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1579-677T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064011 | ||||||
chr14:74064225
|
G | A | 12 | a0003c0003t0003g0189a0005c0006t0001g0131a0005c0006t0001g0132others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579-463G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064225 | ||||||
chr14:74064230
|
G | A | 4 | a0005c0006t0006g0193a0005c0006t0006g0194a0005c0006t0006g0195others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579-458G>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064230 | ||||||
chr14:74064263
|
A | G | 1 | a0003c0003t0001g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1579-425A>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064263 | ||||||
chr14:74064292
|
T | C | 230 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(227): Show | 231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1579-396T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064292 | ||||||
chr14:74064297
|
C | CA | 65 | a0000c0018t0003g0175a0001c0001t0003g0149a0001c0001t0003g0150others(62): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1579-377dupA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74064297 | |||||
chr14:74064297
|
CA | C | 12 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0319others(9): Show | 12 | HG03669.hp2 HG03688.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.1579-377delA | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 74064297 | |||||
chr14:74064309
|
A | AT | 5 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0171others(2): Show | 5 | HG01074.hp2 HG01081.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-379_1579-378i others(3): Show |
BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064309 | ||||||
chr14:74064309
|
A | T | 10 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0146others(7): Show | 10 | HG01884.hp2 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1579-379A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064309 | ||||||
chr14:74064311
|
AT | A | 142 | a0001c0001t0002g0003a0001c0001t0002g0292a0001c0001t0002g0297others(139): Show | 143 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1579-376delT | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064311 | ||||||
chr14:74064312
|
T | A | 66 | a0001c0001t0002g0338a0001c0001t0003g0151a0001c0001t0003g0153others(63): Show | 67 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1579-376T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064312 | ||||||
chr14:74064314
|
A | T | 1 | a0003c0003t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1579-374A>T | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064314 | ||||||
chr14:74064315
|
T | A | 59 | a0002c0002t0014g0238a0003c0003t0001g0008a0003c0003t0001g0009others(56): Show | 59 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1579-373T>A | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064315 | ||||||
chr14:74064352
|
C | G | 135 | a0000c0018t0003g0175a0001c0001t0002g0003a0001c0001t0002g0292others(132): Show | 136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1579-336C>G | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064352 | ||||||
chr14:74064661
|
T | C | 3 | a0004c0007t0003g0361a0004c0007t0003g0364a0004c0007t0003g0365 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1579-27T>C | BBOF1 | ENSG00000119636.16 | transcript | ENST00000394009.5 | protein_coding | 11/11 | chr14 | 74064661 |